Lie Yuan
Yongqing Cai
Liang Zhang1,2,3
Xiaoli Li- 1Department of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, China
- 2Chongqing Key Laboratory of Drug Metabolism, Chongqing, China
- 3Key Laboratory for Biochemistry and Molecular Pharmacology of Chongqing, Chongqing, China
- 4Department of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China
- 5Department of Pharmacy, Fengdu County Hospital of Traditional Chinese Medicine, Chongqing, China
Breast cancer is one of the top-ranked malignant carcinomas associated with morbidity and mortality in women worldwide. Chemotherapy is one of the main approaches to breast cancer treatment. Breast cancer initially responds to traditional first- and second-line drugs (aromatase inhibitor, tamoxifen, and carboplatin), but eventually acquires resistance, and certain patients relapse within 5 years. Chemotherapeutic drugs also have obvious toxic effects. In recent years, natural products have been widely used in breast cancer research because of their low side effects, low toxicity, and good efficacy based on their multitarget therapy. Apoptosis, a programmed cell death, occurs as a normal and controlled process that promotes cell growth and death. Inducing apoptosis is an important strategy to control excessive breast cancer cell proliferation. Accumulating evidence has revealed that natural products become increasingly important in breast cancer treatment by suppressing cell apoptosis. In this study, we reviewed current studies on natural product–induced breast cancer cell apoptosis and summarized the proapoptosis mechanisms including mitochondrial, FasL/Fas, PI3K/AKT, reactive oxygen species, and mitogen-activated protein kinase–mediated pathway. We hope that our review can provide direction in the search for candidate drugs derived from natural products to treat breast cancer by promoting cell apoptosis.
Introduction
Breast cancer (BC) is one of the most common malignancies occurring in women, with its morbidity increasing annually, thereby threatening human health (Georgalas et al., 2015). BC is characterized by high incidence, high mortality, high heterogeneity, high recurrence rate, and poor prognosis (Qian et al., 2019), which have collectively led to its morbidity and mortality surpassing that of lung cancer in women (Sung et al., 2021).
BC can mainly be divided into three subtypes according to histopathological features: estrogen receptor–positive (ER+), HER2-positive (HER2+), and triple-negative (TN). ER+ BC can be treated with tamoxifen and aromatase inhibitors. HER2+ BC can be treated with monoclonal antibodies against HER2, such as trastuzumab. TNBC does not express specific molecules; therefore, standard cytotoxic chemotherapy (doxorubicin, docetaxel, 5-fluorouracil, platinum drugs, and other agents in different combinations) remains the standard of care for patients with TNBC (Nøhr-Nielsen et al., 2020; Su et al., 2020; Pal and Rakshit, 2021; Shimanuki et al., 2021). However, regardless of the treatment strategy, the potential side effects, including lymphedema, weight reduction, pain, and chemotherapy-induced peripheral neuropathy, are significant (Binkley et al., 2012). Furthermore, BC initially responds to traditional chemotherapy. However, it eventually acquires resistance and metastasis in the advanced stage. Moreover, certain patients relapse within 5 years. Therefore, the discovery of additional or substituted drugs to treat BC is urgently required.
In the last 2 decades, natural products, such as alkaloids, flavonoids, terpenoids, and phenylpropanoids, have been widely used in preclinical studies of BC because of their rich natural resources, low toxicity and good efficacy (Ateba et al., 2018; Hematpoor et al., 2018; Kushwaha et al., 2020; Sindhu et al., 2021). They can target various apoptosis-related signaling pathways (PI3K/AKT, mitogen-activated protein kinase [MAPK], and p53) to induce apoptosis in BC cells (Khojasteh Poor et al., 2021; Li et al., 2021). Therefore, natural products are an important resource in the search for candidate drugs to treat BC. However, there is no systematic analysis or review of natural products for treating BC by promoting apoptosis. Herein, the purpose of our review is to summarize the latest research on natural products, including monomers and extracts, on anti-BC treatment through different molecular mechanisms to induce cell apoptosis. We hope that this article will provide direction for follow-up studies of natural products for BC treatment.
Apoptosis and BC
Cell death is indispensable in the growth, development, senescence, and death of an organism (Liu et al., 2018a). It can occur through numerous regulatory mechanisms, including apoptosis, necrosis, necroptosis, pyroptosis, and ferroptosis (Zhang et al., 2021b). Apoptosis and autophagy are known as type I and type II programmed cell death, respectively. Autophagy is a double-edged sword in tumor cells. It can degrade and recycle cellular components in an orderly manner to maintain homeostasis and promote the survival of tumor cells. However, excessive autophagy can lead to autophagic cell death (Yu et al., 2008). Unlike autophagy, apoptosis has been identified as a highly regulated and controlled process that promotes tumor cell death.
Apoptosis is a form of cellular suicide triggered by extracellular (extrinsic apoptosis) or intracellular (intrinsic apoptosis) signals (Suraweera et al., 2020). Its biochemical features include cell contraction, nuclear fragmentation, chromatin aggregation, DNA fragmentation, mRNA decay, and the formation of apoptotic bodies (Roos and Kaina, 2013). Excessive apoptosis leads to atrophy, whereas inadequate apoptosis is associated with uncontrolled cell proliferation, as observed in tumors. In normal breast cells, there is a balance between cell proliferation and apoptosis, antiapoptosis and proapoptosis to maintain the cell homeostasis (Parton et al., 2001). Once the balance is disrupted, activated antiapoptotic signal pathway or proapoptosis pathway deficiency can lead to uncontrolled cell proliferation, therapeutic resistance, and cancer cell recurrence (Mohammad et al., 2015). In BC cells, multiple factors, including growth factor, DNA damage, reactive oxygen species (ROS), and UV radiation, can promote uncontrolled cell growth through mitochondrial, FasL/Fas–, PI3K/AKT–, ROS-, nuclear factor κB (NF-κB)–, and MAPK–mediated pathways, to break the balance of proapoptotic and antiapoptotic effects. Therefore, targeting apoptotic pathways is an efficient strategy for identifying candidate drugs derived from natural products to treat BC (Rajabi et al., 2021).
Proapoptotic Effects of Monomers From Natural Products on BC
An increasing number of studies have comprehensively demonstrated the proapoptotic effects of natural products on BC. In this study, we reviewed the effect and mechanism of monomers derived from natural products on apoptosis in BC (Table 1).
TABLE 1. Proapoptotic effects of monomers from natural products on breast cancer cells.
Mitochondrial Pathway–Mediated Apoptosis
The mitochondrial pathway can be triggered by various cellular stresses, such as UV radiation, DNA damage, ROS, hypoxia, and endoplasmic reticulum stress (ERS). It is also known as an intrinsic pathway that induces apoptosis. The mechanism of mitochondrial pathway–mediated apoptosis is related to altered mitochondrial membrane potential (MMP) and promotes cytochrome c (CytoC) release to activate initiator caspase-9, which then activated caspase-9 cleaves caspase-3, resulting in cell apoptosis. CytoC is regulated by the evolutionarily conserved B-cell lymphoma-2 (Bcl-2) family, which includes proapoptotic and antiapoptotic members (Suraweera et al., 2020). Antiapoptotic members, Bcl-2, Bcl-2–like (Bcl2L), and Bcl-2–related protein long isoform (BclXL), are located in the outer membrane of mitochondria and can prevent the release of CytoC. Proapoptotic members, Bcl-2–associated X-protein (Bax), BH3-interacting death domain (Bid), and Bcl-2–interacting protein (Bim), must be transferred to mitochondria to induce apoptosis.
Numerous studies have suggested that certain natural products induce BC cell apoptosis through the mitochondrial pathway (Figure 1). Ganoderic acid DM is an active monomer of Ganoderma lucidum. In 2012, Wu et al. (2012) reported that ganoderic acid DM significantly induced DNA breakage and poly-ADP-ribose polymerase (PARP) cleavage, reduced MMP, and ultimately induced MCF-7 cell apoptosis. Sharma et al. (2012) also reported that 18β-glycyrrhetinic acid induced apoptosis through the mitochondrial death cascade, characterized by the absence of MMP, promoting the release of CytoC and activation of caspase-9. Stevioside is a diterpenoid glycoside found in Stevia rebaudiana (Bertoni) Bertoni leaves. A study by Paul et al. (2012) revealed that stevioside can reduce MMP and activate the mitochondrial-mediated apoptotic pathway in MCF-7 cells, suggesting that stevioside is a potent inducer of apoptosis. Amentoflavone, isolated from an ethyl acetate extract of Selaginella tamariscina (P. Beauv.) Spring, has been reported to trigger apoptosis of MCF-7 cells by reducing MMP and promoting CytoC release and caspase-3 activation (Pei et al., 2012). In 2013, as shown in the study by Tian et al. (2013), calycosin decreased Bcl-2 and increased Bax expression to incur BC cell apoptosis through the mitochondrial pathway. Rajput et al. (2013) found that thymoquinone, the predominant bioactive ingredient of black seed oil (Nigella sativa L.), could induce apoptosis in MDA-MB-468 and T47D cells through upregulation of the levels of Bax, CytoC, cleaved caspase-3, and cleaved PARP, along with downregulation of the levels of Bcl-2, BclXL, and survivin. Embelin is a small-molecule compound extracted from the Myrsinaceae family. As shown in the study by Li et al. (2013), embelin can regulate Bax and Bcl-2, promote the release of CytoC, and activate caspase-3 and caspase-9, which indicates that the mechanism of embelin-induced MCF-7 apoptosis is related to the mitochondrial pathway. In 2013, Kim et al. reported that ginseng saponin rg3 induced MDA-MB-231 cell apoptosis through typical mitochondria-dependent caspase activation (Kim et al., 2013). In 2014, Ma et al. reported that ursolic acid reduced the proliferation and induced apoptosis of MDA-MB-231 cells by increasing the activities of caspase-3 and caspase-9 via the mitochondrial apoptosis pathway (Ma and Sun, 2014). Kim et al. proposed that dioscin induced apoptosis in MDA-MB-231, MDA-MB-453, and T47D cells by promoting the transfer of apoptosis-inducing factor (AIF) from the mitochondria to the nucleus and inhibiting antiapoptotic proteins Bcl-2, cIAP-1, and Mcl-1 (Kim et al., 2014). As shown in the study by Zhang et al. (2018a), 20(S)-protopanaxadiol (PDD) upregulated the expression of Bax/Bcl-2, cleaved PARP, and downregulated the expression of MMP of MCF-7 cells, and the caspase protein family was activated, indicating that MCF-7 cell apoptosis was induced by PDD via the mitochondrial pathway. Paratocarpin E, which belongs to prenylated chalcone, was extracted from Euphorbia humifusa Wild. In 2016, Gao et al. (2016) reported that paratocarpin E induced apoptosis in MCF-7 cells by altering the expression of Bax and Bcl-2 and inducing the release of CytoC from the mitochondria into the cytoplasm, suggesting that mitochondria-mediated pathways are activated during this process. In 2016, Lee et al. reported that amygdalin induced apoptosis of Hs578T TNBC cells, and the proapoptotic effect may be related to Bcl-2 downregulation, Bax upregulation, caspase-3 activation, and cleaved PARP increase (Lee and Moon, 2016). Cordycepin, a major compound isolated from Cordyceps sinensis (BerK.) Sacc., has been reported to increase the activation of proapoptotic proteins, such as caspase-8, caspase-9, caspase-3, and Bax, and inhibit Bcl-2 expression, suggesting that cordycepin could induce apoptosis in BC cells via the caspase-dependent pathway (Wang et al., 2016). Berberine is an isoquinoline alkaloid isolated from Cotridis rhizoma. In 2017, Zhao et al. (2017) demonstrated that berberine activated caspase-9/CytoC–mediated apoptosis to suppress TNBC cell proliferation in vitro and in vivo. Clematis hederagenin saponin (CHS), isolated from Clematis chinensis Osbeck, is a triterpenoid saponin family. Cheng et al. (2018) reported that CHS could significantly increase mitochondrial Apaf-1 and CytoC to activate caspase-3 and caspase-9 in BC cells and finally showed a proapoptotic effect. In 2019, Zhu et al. reported that kaempferol, a flavonoid, could induce apoptosis in MDA-MB-231 cells, which may be achieved by increasing the expression of cleaved caspase-9/3 and p-ATM (Zhu and Xue, 2019). Liao et al. (2019) demonstrated that diosgenin induced the loss of MMP, resulting in the release of CytoC and activation of the caspase signaling cascade in BC cells. In a 2020 study by Rosas Gonzalez et al.(2020), allicin reduced cell viability and led to apoptosis by activating caspase-3/8/9; upregulating NOXA, p21, and Bak; and downregulating BclXL expression. Ma et al. (2021) found that dehydrocostuslactone suppressed the growth and promoted apoptosis in SK-BR-3 BC cells, which may be associated with the inhibition of the antiapoptotic ability of BC cells by regulating Bax/Bcl-2 and caspase-3 expression.
FIGURE 1. Natural products induced apoptosis through mitochondrial pathway. (1) Kaempferol, (2) berberine, (3) Clematis hederagenin saponin, (4) ursolic acid, (5) ganoderic acid DM, (6) stevioside, (7) Calycosin, (8) thymoquinon, (9) amygdalin, (10) catechol, (11) apigenin, (12) oleuropein, (13) diosgenin, (14) embelin, (15) dioscin, (16) violacein.
Cofilin can regulate mitochondrial division by interacting with Drp1 at mitochondrial division sites, leading to mitochondrial damage and CytoC release and ultimately inducing apoptosis. 4-Methylthiobutyl isothiocyanate (erucin) is a compound isolated from cruciferous vegetables. In 2015, Li et al. (2015) showed that erucin induced mitochondrial division and apoptosis in human BC cells through mitochondrial translocation of cofilin, which was correlated with downregulated PARP and upregulated caspase-3 and caspase-9 cleavage. Li et al. (2017a) reported that polyphyllin I induced mitochondrial translocation of DRP1 by dephosphorylating the Ser637 site of DRP1, leading to mitochondrial division and CytoC release from mitochondria into the cytoplasm, ultimately leading to BC cell apoptosis. Arnidiol is a pentacyclic triterpenoid diol. In 2020, Hu et al. (2020) found that arnidiol induced apoptosis in human BC MDA-MB-231 cells via mitochondrial translocation of Drp1 and cofilin, which was correlated with reduced PARP expression and increased caspase-3 cleavage. Furthermore, in 2021, Shen et al. (2021) revealed that coadministration of cepharanthine and epirubicin markedly led to mitochondrial translocation of cofilin, thus inducing apoptosis in TNBC cells via the mitochondrial pathway.
P53 is a nuclear transcription factor that is negatively and positively regulated by MDM2 and ATM, respectively, and can regulate apoptosis-related gene expression, such as that of Bax and BclXL, to exhibit an anti-BC effect. P53 can also alter MMP and trigger CytoC release, ultimately inducing BC cell apoptosis via the mitochondrial pathway. The deficiency of p53 reduces the therapeutic effect and prognosis of BC. Therefore, accumulating evidence has shown that many natural products can increase or stabilize p53 to induce BC apoptosis. Liu et al. (2012) proposed that apigenin induced p53-dependent apoptosis in BC T47D cells. In 2014, Patel et al. revealed that l-carvone induced p53- and caspase-3–mediated apoptosis in MCF-7 and MDA-MB-231 cells (Patel and Thakkar, 2014). In 2014, Hassan et al. proposed that oleuropein-induced apoptosis via the p53 pathway in MCF-7 cells was related to the upregulation of p53 and Bax and downregulation of Bcl-2 (Hassan et al., 2014). In 2015, Zu et al. reported that emodin reduced Bcl-2 levels and increased cleaved caspase-3, PARP, p53, and Bax levels in BCAP-37 and ZR-75-30 BC cells, suggesting that it could induce apoptosis through the p53-mediated mitochondrial pathway (Zu et al., 2015). Gaillardin is a natural sesquiterpene lactone. In 2015, Fallahian et al. found that the mechanism of apoptosis induced by gaillardin in MCF-7 and MDA-MB-468 cells involved upregulation the expression of Bax and p53, increased the production of ROS, and downregulated the expression of Bcl-2, inducing the loss of MMP (Fallahian et al., 2015). Sesamin is a major component of Sesamum indicum L. In 2015, Siao et al. demonstrated that sesamin could cause apoptosis in BC cells MCF-7 by improving the expression of the apoptosis markers Bax, caspase-3, and p53 (Siao et al., 2015). Zhang et al. found that osthole induced apoptosis in MCF-7 cells by the p53 pathway, which was related to high expression of Bax, p53, p21, and CytoC, as well as downregulation of Bcl-2 and MMP (Zhang and Zhu, 2016). Feng et al. (2016) showed that high concentrations of arecoline resulted in MCF-7 cell apoptosis, which may be achieved by increasing the protein expression of p53 and Bax and decreasing that of Bcl-2. Violacein is a natural purple pigment produced primarily by microorganisms. Alshatwi et al. (2016) showed that violacein induced apoptosis in MCF-7 cells through the upregulation the levels of Bax and p53 and downregulation the levels of MDM2. Li et al. (2017b) demonstrated that the mechanism of apoptosis induced by liriodenine in MCF-7 cells inhibited the expression of Bcl-2, cyclin D1, and vascular endothelial growth factor (VEGF) and upregulated the level of p53. As shown in the study by Liang et al. (2021), resveratrol can facilitate TNBC cell apoptosis via the p53-mediated pathway. In 2021, a study by Vazhappilly et al. indicated that catechol could inhibit proliferation and result in apoptosis in MCF-7 cells by activating p53, inhibiting of regulatory proteins such as DNMT1, P-BRCA1, Mcl-1, and PDCD6, and increasing the Bax/Bcl-2 ratio. Ultimately, caspase-mediated cell death is triggered (Vazhappilly et al., 2021). In their study, Sp et al. (2021) showed that 6-zingerol might induce apoptosis in MDA-MB-231 and MCF-7 BC cell lines by activating p53, regulating the Bax/Bcl-2 ratio, and increasing the release of CytoC.
Mitochondria are the main sites of ROS production. Accumulated ROS can directly act on the mitochondrial membrane, induce changes in MMP, release CytoC and other AIFs, and finally activate the caspase cascade, leading to apoptosis. 3β, 6β, 16β-trihydroxylup-20 (29)-ene (TTHL) is a pentacyclic triterpene isolated from the medicinal plant Combretum leprosum Mart. In 2014, Viau et al. demonstrated that TTHL induced MCF-7 cell apoptosis, and TTHL-induced apoptosis was accompanied by increased caspase-9 and intracellular ROS (Viau et al., 2014). Baicalein is a natural flavonoid extracted from Scutellaria baicalensis Georgi. A study by Liu et al. (2019) showed that baicalein damaged MMP, downregulated antiapoptotic protein Bcl-2 expression, upregulated proapoptotic protein Bax expression, and promoted the release of CytoC and activated caspase-9/3 in BC cells by increasing intracellular ROS levels. In a study conducted by Wang et al. (2020), diosmetin significantly upregulated the protein expression of p53, Bax, and caspase-3; downregulated the protein expression of Bcl-2; reduced MMP; and promoted ROS accumulation in MCF-7 cells, suggesting that diosmetin may promote apoptosis in MCF-7 cells through ROS- and p53-mediated mitochondrial apoptosis pathways.
FasL-Fas–Mediated Apoptosis
Upon FasL binding to the Fas receptor, it causes the formation of the complex of Fas, FADD, and pro–caspase-8, known as the death-inducing signaling complex. After caspase-8 is activated through self-cleavage of pro–caspase-8, it subsequently activates downstream effectors, including caspase-3 and caspase-7, resulting in cell apoptosis. Therefore, targeting to the FasL-Fas pathway is one of the strategies to induce cell apoptosis. Certain natural products have been shown to activate the FasL-Fas pathway to induce apoptosis in BC cells (Figure 2).
FIGURE 2. Natural products induced apoptosis through FasL-Fas pathway. (1) Fraxetin, (2) gambogenic acid, (3) icariside II, (4) pulveraven A.
In 2012, Huang et al. (2012) reported that icariside II enhanced the expression of Fas and FADD, activated caspase-8 in MCF-7 BC cells, and played a role in promoting apoptosis. Gambogenic acid is the main active component isolated from the tree Garcinia hanburyi Hook. f. In 2013, Zhou et al. (2013) proposed that gambogic acid could induce BC cell apoptosis, and the mechanism was also related to increased expression of Fas, cleaved caspase-3/8/9, and Bax and decreased expression of antiapoptotic protein Bcl-2. In 2013, Wang et al. (2013a) proposed that genistein enhanced FasL, FADD, and cleaved caspase-8 protein expression in MDA-MB-231 cells, suggesting that genistein-induced apoptosis was mediated by the Fas/FasL pathway. In 2014, Li et al. (2014) demonstrated that α-mangostin significantly inhibited the expression of Fas and intracellular Fas activity to induce apoptosis in BC cells. In 2017, Liu et al. (2017a) reported that fraxetin suppressed cell proliferation and induced MCF-7 cell apoptosis by increasing the expression of Fas, FasL, and Bax and reducing Bcl-2 expression. Pulveraven A is a phenolic compound isolated from Pulveroboletus ravenelii. In 2021, Lee et al. proposed that apoptotic BC death was induced by the activation of promoter caspase-8 and executioner caspase-7 and upregulated the expression of FADD by pulveraven A. Furthermore, it was accompanied by an increase in the Bax/Bcl-2 ratio (Lee et al., 2021).
PI3K/AKT Pathway Mediated Apoptosis
The PI3K/AKT pathway is triggered by the binding of ligands, such as insulin, growth factors, and hormones. Upon PI3K activation, it phosphorylates AKT, and activated AKT plays an important role in regulating Bad, a proapoptotic member of the Bcl-2 family, to inhibit mitochondrial-mediated apoptosis. Alternatively, activated AKT phosphorylates other components, such as the mTOR complex and IkBα/NF-κB, which are ultimately involved in cell growth (Miricescu et al., 2020). Therefore, targeted inhibition of PI3K/AKT pathway activation can promote cell apoptosis. In recent decades, increasing evidence has indicated that nature produces can inactivate PI3K/AKT pathway to induce BC apoptosis (Figure 3).
FIGURE 3. Natural products induced apoptosis through PI3K/AKT pathway. (1) cepharanthine, (2) piperlongumine, (3) fangchinoline, (4) lycopene, (5) genistein, (6) ramentaceone, (7) baicalein, (8) 18β-glycyrrhetinic acid, (9) tetramethylpyrazine, (10) cucurbitacin e, (11) ramentaceone, (12) baicalein, (13) daucosterol linoleate, (14) kaempferol, (15) flavopereirine.
In 2012, Sharma et al. (2012) reported that 18-β-glycyrrhetinic acid induced apoptosis by modulating the AKT/Foxo3a/Bim pathway in MCF-7 cells. In 2015, Hu et al. (2015) showed that isorhamnetin had a proapoptotic effect in MCF-7 and MDA-MB-468 BC cells, which was mediated by the AKT and MEK signaling pathways. In 2015, another report by Chen et al. (2015c) suggested that the phosphorylation level of AKT and the expression of its downstream target protein HOTAIR were decreased after treatment with calycosin, thus inducing apoptosis in MCF-7 BC cells. In 2016, Peng et al. (2016) proposed that ginsenoside Rg3 promoted apoptosis in BC cells by interfering with the level of mammaglobin A in MDA-MB-231 cells, and this effect was achieved by affecting PI3K/AKT signaling pathway activity. α-Mangostin was extracted from mangosteen (Garcinia mangostana L.). In 2016, Kritsanawong et al. (2016) found that α-mangostin induced apoptosis in BC cells, which may be associated with PI3K/AKT signaling pathway regulation. Stachydrine hydrochloride is a well-known bioactive ingredient extracted from Leonurus cardiac L. Wang et al. (2017) reported that stachydrine hydrochloride inhibited cell division and growth and induced apoptosis in BC cells via deactivation of the AKT and ERK pathways. As a rare ginsenoside and the main ingredient extracted from fine black Panax ginseng C.A.Mey., ginsenoside Rg5, can induce apoptosis in a dose-dependent manner by inhibiting p-PI3K and p-AKT in vivo (Liu and Fan, 2018). In 2018, Liu et al. (2018b) reported that galangin inhibited MCF-7 cell proliferation and induced cell apoptosis via the mitochondrial and PI3K/AKT pathways. In 2018, Shen et al. (2018) showed that tetramethylpyrazine could significantly decrease the gene expression and the activity of AKT and increase the activity of caspase-3, thus inducing apoptosis in BC cells. Daucosterol linoleate, a steroid extracted from Manihot esculenta Crantz, has been reported to diminish the expression of the antiapoptotic proteins BclXL, Bcl-2, and XIAP; promote the levels of proapoptotic proteins Bax and Bad; and activate caspase-dependent apoptosis in vivo. Moreover, daucosterol linoleate invalidates the upstream of the PI3k/AKT/NF-κB pathway (Han et al., 2018). Crambescidin, separated from Monanchora viridis, a marine sponge, may be involved in the inactivation of phosphorylation of Akt, NF-κB, and MAPK pathways, resulting in apoptosis in TNBC cells according to the study by Shrestha et al. (2018). In 2019, Zhao et al. (2019) showed that kaempferol promoted the apoptosis of the SUM190 inflammatory BC cell line, and the proapoptotic effect might be associated with PI3K/AKT/GSK-3β pathway inhibition. Flavopereirine is a β-carboline alkaloid with antiplasmodial activity. In 2019, Yeh et al. (2019) reported that flavopereirine can induce apoptosis in MDA-MB-231cells by inhibiting the AKT/p38/ERK pathway. In 2021, Xu et al. (2021) reported that erianin can induce TNBC cell apoptosis, which may be ascribed to the inhibition of the PI3K/AKT pathway.
mTOR is one of the downstream members of the PI3K/AKT signaling pathway and is directly regulated by AKT. Activation of mTOR can phosphorylate p70S6K and 4EBP1 to promote cell survival. In 2017, Zhang et al. discovered that fangchinoline induced apoptosis in MDA-MB-231 cells. The mechanism was related to the downregulation of PI3K, AKT, mTOR, and p-PI3K, p-AKT, and p-mTOR proteins in a concentration-dependent manner (Zhang et al., 2017). In 2014, Takeshima et al. (2014) proposed that lycopene induced apoptosis in the MDA-MB-468 cell line by inhibiting the phosphorylation of AKT and its downstream molecule mTOR, enhancing PARP cleavage and upregulating Bax. In 2014, Shrivastava et al. proposed that piperlongumine, an alkaloid, reduced the expression of p-AKT, p70S6K1, 4EBP1, Bcl-2, and p53 and increased the expression of Bax and CytoC in human TNBC cells, suggesting that the proapoptotic function of piperlongumine was related to the inhibition of the PI3K/AKT/mTOR signaling axis (Shrivastava et al., 2014). Cepharanthine is a biscoclaurine alkaloid extracted from Stephania cephalantha Hayata. In 2017, Gao et al. (2017) reported that cepharanthine resulted in apoptosis in MCF-7 and MDA-MB-231 cells, which might be achieved by AKT/mTOR signaling pathway inhibition. In 2017, Sun et al. proposed that fisetin reduced the phosphorylation of PI3K, AKT, mTOR, and p70S6K and upregulated apoptosis factors such as Bax and caspase-3/8/9 in BC cells. These results indicated that fisetin inhibited cell growth and induced the apoptosis, which was attributed to the inhibition of the PI3K/AKT/mTOR signaling pathway (Sun et al., 2018). Paris saponins are saponin compounds isolated from Paris polyphylla Sm. A study by Xie et al. showed that the apoptotic effect of Paris saponins in BC cells was mediated through the Akt/mTOR signaling pathway. It was highly correlated with the downregulation of p-AKT, p-mTOR, p-P70S6K, and p-4EBP1 (Xie et al., 2017). According to another study by Yan et al., baicalein significantly reduced the expression of p-AKT, p-mTOR, NF-κB, and p-IκB in MCF-7 and MDA-MB-231 cells, demonstrating that baicalein can induce BC cell line apoptosis in animal models by inhibiting the PI3K/AKT signaling pathway (Yan et al., 2018). 20(S)-PPD belongs to one of the main active metabolites of Panax ginseng C.A.Mey. In 2018, Zhang et al. (2018a) reported that 20(S)-PPD could downregulate the protein expression of PI3K/AKT/mTOR in MCF-7 cells. In 2018, Sultan et al. (2018) reported that cannabidiol suppressed cell survival and prompted apoptosis in a dose-dependent manner, accompanied by downregulation of mTOR and upregulation and localization of PPARγ protein in the nuclei and cytoplasm. In 2018, another report by Hu et al. (2018) indicated that curcumin inhibited the phosphorylation of AKT and mTOR, decreased Bcl-2 and increased Bax, and cleaved caspase-3, subsequently inducing apoptosis in MCF-7 and MDA-MB-231 cells. In 2020, Wei et al. (2020) proposed that magnoflorine, a quaternary alkaloid separated from Schisandra chinensis (Turcz.) Baill or Aristolochia clematitis L., improved cell sensitivity to doxorubicin by inducing apoptosis through the Akt/mTOR and p38 signaling pathways.
Bcl-2 family proteins, which play a key role in determining cell death or survival, are downstream targets of AKT. For example, AKT directly phosphorylates Bad, which is then separated from Bcl-2. Then, Bcl-2 binds to the proapoptotic Bcl-2 family members such as Bax and Bak, thereby inhibiting apoptosis. In 2014, Kong et al. (2014) reported that cucurbitacin E can induce the MDA-MB-468 cell apoptosis by reducing the levels of cyclin D1, survivin, XIAP, Bcl-2, and Mcl-1 and inhibiting the activation of AKT. d-Rhamnose β hederin is an oleanane-type triterpenoid soap, which was found to induce apoptosis in BC cells by inhibiting the PI3K/AKT signaling pathway and regulating the protein expression of the Bcl-2 family (Cheng et al., 2014). Genistein, an estrogenic soy-derived compound, belongs to the isoflavone family. In 2015, Chen et al. (2015b) proposed that genistein induced apoptosis via the IGF-1R/p-Akt signaling pathway in MCF-7 cells, accompanied by a reduction in the ratio of Bcl-2/Bax. Ramentaceone, a naphthoquinone isolated from Drosera rotundifolia L., was reported to induce BC cell apoptosis by inhibiting the PI3K/AKT signaling pathway, which was highly correlated with upregulated Bax and Bak expression, downregulated Bcl-2 expression, and inhibition of PI3K and AKT phosphorylation (Kawiak and Lojkowska, 2016). A study by Razak et al. (2019) showed that eupatorine-induced apoptosis in MCF-7 and MDA-MB-231 cells was mediated by the upregulation of proapoptotic genes such as Bak1, HIF1A, Bax, and Bad, increasing CytoC release and SMAC/Diablo and blocking the p-AKT pathway. Hong et al. showed that ginsenoside Rk1 increased the levels of Bax, CytoC, and cleaved caspase-3/8/9 and reduced Bcl-2 by blocking the PI3K/AKT pathway (Hong and Fan, 2019). In 2019, Han et al. (2019) showed that parthenolide could lead to BC cell apoptosis by modulating the PI3K/AKT signaling pathway, which was highly correlated with downregulated Bcl-2 expression and upregulated cleaved caspase-3 expression. In 2020, Yu et al. proposed that avicularin induces MDA-MB-231 cell apoptosis, which may be associated with the inhibition of the PI3K/AKT signaling pathway to decrease the gene expression of Bcl-2, BclXL, and CDK2 (Yu et al., 2020).
MAPK Pathway–Mediated Apoptosis
MAPK pathways are sequentially phosphorylated and activated by three protein kinases: MAPKKK activates MAPKK, which then activates MAPK. MAPKs are traditionally classified as ERK, JNK, and p38 kinase in mammalian cells. Through cascade reactions, MAPKs can transmit extracellular and intracellular signals to regulate cell growth, proliferation, differentiation, migration, and apoptosis.
Accumulating evidence suggests that MAPKs are important targets in natural product–induced BC cell apoptosis (Figure 4). In 2012, Chen and Sun found that formononetin elevated the Bax/Bcl-2 ratio in MCF-7 cells by activating the Ras-p38MAPK signaling pathway and finally induced cell apoptosis (Chen and Sun, 2012). Kim et al. reported that genipin, a constituent of Gardenia jasminoides J. Ellis, downregulated Bcl-2 and upregulated Bax and cleaved caspase-3 by activation of p38 and JNK signals, suggesting that genipin induced MDA-MB-231 cell apoptosis mediated by MAPK pathway activation (Kim et al., 2012). Deoxypodophyllotoxin (DTP) is a natural ingredient extracted from Juniperus communis L. In 2015, Benzina et al. proposed that DTP can induce BC cell apoptosis by inactivation of the ERK and NF-κB signaling pathways (Benzina et al., 2015). In 2015, Fan et al. (2015) proposed that emodin suppressed MCF-7 cell proliferation, and further studies showed that emodin promoted MCF-7 cell apoptosis by activating the JNK-AP1 signal transduction pathway. In 2015, Ranganathan et al. (2015) demonstrated that quercetin significantly inhibited cyclin D1, p21, Twist, and p-p38 expression in MCF-7 cells, demonstrating that quercetin increased BC cell apoptosis through the p38-Twist pathway mediated by cell cycle arrest. In 2017, Nguyen et al. also found that quercetin increased the signaling activities of p53, p21, and GADD45, and Foxo3a protein and mRNA expression and induced nuclear translocation of Foxo3a. The JNK inhibitor abolished quercetin-stimulated Foxo3a activity and apoptosis, suggesting that quercetin induced apoptosis by regulating Foxo3a signaling in TNBC cells (Nguyen et al., 2017). Isocryptotanshinone is a natural bioactive component isolated from Salvia miltiorrhiza Bunge. In 2015, Zhang et al. reported that isocryptotanshinone promoted apoptosis in human MCF-7 BC cells by activating MAPK signaling pathways, including p38, ERK, and JNK (Zhang et al., 2015a). In 2016, as shown in the study by Lai et al., tetramethylpyrazine (TMP) improved the expression of p-p38 and p-JNK proteins. However, it reduced p-ERK expression in MCF-7 cells. TMP can induce apoptosis in MCF-7 cells, and this may be related to MAPK signaling pathway activation (Lai et al., 2016). α-Mangostin was extracted from Garcinia mangostana L., and in 2016, Kritsanawong et al. (2016) found that α-mangostin could promote BC cell apoptosis by inhibiting PI3K/AKT and increasing p38 and JNK activation. In 2017, Lee et al. found that gallic acid decreased the expression of cyclin D1/CDK4 and cyclin E/CDK2, increased the expression of p21 and p27, and induced the activation of caspase-3/9 in MDA-MB-231 cells. In addition, p38 was found to be involved in gallic acid–induced apoptosis. The results indicated that gallic acid–induced apoptosis was related to the p38/p21/p27 axis (Lee et al., 2017). In 2019, Huang et al. (2019) reported that sophoraflavanone G suppressed the MAPK-related pathway to increase cleaved caspase-3/8/9 and Bax expression, decrease Bcl-2 and BclXL expression, and prompt the release of CytoC from mitochondria to the cytoplasm in MDA-MB-231 cells. Cardamonin is natural chalcone separated from large black Elettaria cardamomum (L.) Maton. As shown in the study by Kong et al. (2019), cardamonin increased the expression of Foxo3a and its target genes p21, p27, and Bim, and further studies suggested that cardamonin induced BC cell apoptosis by activating the JNK-Foxo3a pathway. In 2021, another report by Kim et al. (2021) indicated that silymarin induced BC cell apoptosis by regulating the MAPK signaling pathway, which increased the levels of Bax, cleaved PARP, cleaved caspase-9, and p-JNK and reduced the levels of Bcl-2, p-p38, and p-ERK.
FIGURE 4. Natural products induced apoptosis through MAPK pathway. (1) Tetramethylpyrazine, (2) emodin, (3) quercetin, (4) Deoxypodophyllotoxin.
NF-κB–Mediated Apoptosis
NF-κB can be activated physiologically and pathologically, such as by growth factors and oxidant-free radicals, particularly by pro-inflammatory cytokines interleukin 1 (IL-1) and tumor necrosis factor (TNF). Binding to the receptor TNFR1, TNF can recruit TNF-associated receptor death domain that binds to the TNF receptor–associated factor 2 and the kinase receptor–interacting protein 1, and then recruit IκB kinase (IKK), leading to the phosphorylation and subsequent degradation of IκBα, which activates NF-κB translocation into the nucleus, thereby regulating related gene expression to regulate cell apoptosis.
In 2013, Wang et al. (2013b) demonstrated that oridonin induced MDA-MB-231 BC cell apoptosis, which was associated with a reduction in the Bcl-2/Bax ratio, caspase-8, NF-κBp65, IKKα, IKKβ, and p-mTOR, and upregulated cleaved PARP, PPAR, and Fas expression levels. In 2018, Wu et al. (2018b) proposed that delphintin significantly downregulated the expression of p-NF-κBp65, p-IκBα, p-IKKα/β, and p-PKCα in MDA-MB-453 and BT-474 BC cells. The results showed that delphintin induced apoptosis by blocking the NF-κB signaling pathway. In 2018, Ren et al. demonstrated that chrysophanol upregulated caspase-3 and PARP cleavage and downregulated the apoptosis regulators Bcl-2, p-NF-κBp65, and p-IκB, which indicated that the proapoptotic function of chrysophanol was achieved by regulating the NF-κB/Bcl-2 signaling cascade (Ren et al., 2018). In 2021, Chen et al. found that capsaicin significantly reduced the expression of FBI-1, Ki-67, Bcl-2, and survivin; increased Bax protein expression; and activated caspase-3 in BC cells. Furthermore, NF-κB, the target gene of FBI-1, was also inactivated by capsaicin treatment. These results indicate that the proapoptotic effect of capsaicin is related to the FBI-1–mediated NF-κB pathway (Chen et al., 2021).
ROS-Mediated Apoptosis
Intracellular ROS can induce apoptosis through several signal pathways. First, ROS can cause oxidative damage to all mitochondrial components. Damaged mitochondrial DNA disrupts mitochondrial oxidative phosphorylation, thus increasing MMP and releasing CytoC to contribute to cell death. In addition, ROS can activate JNK and p38 and trigger mitochondria-mediated apoptosis. Moreover, Foxo3a is a nuclear transcription factor, and ROS can promote the translocation of Foxo3a, which regulates apoptosis-related gene expression. However, ROS can increase NF-κB activation and inhibit apoptosis. Hence, ROS-mediated apoptosis may increase with the use of natural components (Figure 5).
FIGURE 5. Natural products induced apoptosis through ROS pathway. (1) Crocin, (2) geraniin, (3) ziyuglycoside II, (4) hyperoside.
In 2014, a study showed that ziyuglycoside II treatment induced BC cell apoptosis by activating the ROS/JNK pathway (Zhu et al., 2014). In 2015, Xie et al. proposed that berberine also increased the production of ROS in MCF-7 and MDA-MB-231 cells, which promoted proapoptotic JNK signaling. Phosphorylated JNK triggers MMP depolarization and Bcl-2 downregulation, concomitant with the Bax upregulation, and release of CytoC and AIF from mitochondria, eventually leading to apoptosis (Xie et al., 2015). Geraniin, a typical ellagitannin extracted from Phyllanthus urinaria L., was found to contain a series of bioactive. In 2016, Zhai et al. (2016) reported that geraniin could generate intracellular ROS and activate p38, and inhibition of ROS can restrain the phosphorylation of p38 and reverse geraniin-induced apoptosis, which suggests that geraniin results in MCF-7 cell apoptosis via the ROS–p38 pathway. In 2019, Qiu et al. (2019) proposed that hyperoside induced apoptosis in MCF-7 and 4T1 cells through the ROS-mediated NF-κB signaling pathway, which was attributed to reduced levels of Bcl-2 and XIAP, and increased the expression of Bax and cleaved caspase-3. In 2020, Nasimian et al. found that crocin induced apoptosis in MCF-7 and MDA-MB-231 cells. The ROS-activated Foxo3a cascade played a crucial role in this process, and Foxo3a-mediated upregulation of PTEN further inhibited the AKT pathway (Nasimian et al., 2020).
Mitochondria are the primary site of ROS production and are also one of the most sensitive targets of ROS action. Intracellular ROS accumulation can activate the mitochondria-mediated apoptosis pathway. Fucoidan is an active ingredient in seaweeds. In 2013, according to the study by Banafa et al. (2013), fucoidan induced MCF-7 cell apoptosis by upregulating caspase-8 and Bax, downregulating Bcl-2, and increasing the release of CytoC and the production of ROS. Looi et al. also reported in 2013 that vernodalin can induce MCF-7 cell apoptosis by increasing the production of ROS in human BC cells, thereby inducing the reduction of MMP and the release of CytoC, thus triggering the caspase cascade and PARP cleavage (Looi et al., 2013). Tetrandrine is an alkaloid that is known for its anticancer activity. In 2020, N et al. (2019) demonstrated that tetrandrine separated from Cyclea peltata (Lam.) Hook. f. and Thomson induced cytotoxicity and apoptosis by increasing ROS and caspase-8/9/3 in MDA-MB-231 cells. Pereyra-Vergara et al. (2020) reported that apoptosis induced by (−)-epicatechin in human BC cells was mediated by ROS to increase the proapoptotic proteins Bad and Bax. In 2020, Jia et al. (2020) proposed that formononetin could induce mitochondrial damage and decrease MMP in BC cells by inhibiting antioxidant enzyme activity and increasing ROS levels, ultimately activating caspase-3-mediated apoptosis.
JAK-STAT3–Mediated Apoptosis
JAK/STAT signaling can transfer an extracellular signal into a transcriptional response that contributes to cancer progression and metastatic development. IL-6, epidermal growth factor (EGF), interferon-α, and other extracellular signals can stimulate the activation of JAK2 and STAT3. Phosphorylated STAT3 then enters the nucleus; dimerized STAT3 binding to specific regulatory sequences could activate or inhibit transcription of target genes, such as BclXL, p21, and Myc, to regulate cell apoptosis.
For natural products, inhibiting the JAK/STAT3 pathway may be a potential strategy to induce BC cell apoptosis. In 2014, Xu et al. reported that apigenin can induce MDA-MB-453 cell apoptosis by upregulating cleaved caspase-8/3 and PARP, blocking the activation (phosphorylation) of JAK2 and STAT3, and decreasing the nuclear tillering of STAT3 (Seo et al., 2014). In 2015, Zhang et al. demonstrated that berberine upregulated Bax, cleaved PARP, and caspase-3 and downregulated p-JAK2, p-STAT3, and Bcl-2 levels. Berberine may induce MCF-7 cell apoptosis by regulating JAK2/STAT3 signaling in a concentration-dependent manner (Zhang et al., 2015b). 7β-(3-ethyl-cis-crotonoyloxy)-1α-(2-methylbutyryloxy)-3,14-dehydro-Z-notonipetranone, an ingredient isolated from Tussilago farfara L., was found to induce BC cell apoptosis by inhibiting JAK-STAT3 signaling and the expression of STAT3 target genes (Jang et al., 2019). In a study conducted by Ma et al. (2020), it was found that the mRNA expression of JAK2 and STAT3 was significantly decreased after curcumol treatment, suggesting that curcumol-induced apoptosis in BC cells might be realized through inhibition of the JAK2/STAT3 signaling pathway. In a study conducted in 2021, Feng et al. proposed that saikosaponin D can suppress cell growth and induce MCF-7 cell apoptosis, which may also be related to the JAK2/STAT3 pathway (Feng et al., 2021).
Endoplasmic Reticulum Stress–Mediated Apoptosis
Hypoxia, starvation, Ca2+ imbalance, and other factors can induce ERS. During the ERS phase, PERK dissociates from GRP78/BiP and is activated by phosphorylation. PERK activation also leads to increased translation of transcription factors, such as ATF4, which further promotes the synthesis of the proapoptotic factor CHOP. CHOP downregulates the antiapoptotic protein Bcl-2 and promotes apoptosis. Moreover, CHOP promotes GADD45 expression, which triggers apoptosis by completely blocking protein synthesis. In 2014, Hou et al. (2014) proposed that fucoxanthin upregulated intracellular free calcium content and the activation of calpain in MCF-7 cells through ERS pathway, and treatment with fucoxanthin also promoted the activation of caspase-4/7/9 and release of CytoC, thereby inducing BC cell apoptosis. In 2020, Li et al. (2020) proposed that oleandrin can induce apoptosis of MCF-7 cells by downregulating Bcl-2 and upregulating Bax, Bim, and ERS-related proteins such as EIF2α, ATF4, and CHOP, suggesting that ERS plays an important role in this process. In 2018, Wu et al. (2018b) proposed that salviaflaside can induce MDA-MB-231 cell apoptosis by activating the ERS response to upregulate GRP78/CHOP and interfere with the Bcl-2/Bax balance.
Other Pathway–Mediated Apoptosis
Multiple other signaling pathways can regulate BC cell apoptosis, such as the Wnt/β-catenin, Notch, and sirtuin-1 pathways. In 2012, curcumin, as the main ingredient of the spice turmeric isolated from the rhizomes of the plant Curcuma longa L., was reported to induce TNBC cell apoptosis by decreasing EGF receptor expression (Sun et al., 2012). In 2017, Zhao et al. (2017) also showed that curcumin suppressed cell growth and led to apoptosis in BT549 cells, and the mechanism was related to the inhibition of the Wnt/β-catenin signaling pathway. In 2014, Shao et al. (2014) reported that triptolide, a diterpene triepoxide compound, induced apoptosis via the Wnt/β-catenin signaling pathway. Ursolic acid is a natural pentacyclic triterpenoid compound. In 2012, Wang et al. (2012) demonstrated that ursolic acid inhibited FoxM1 expression and induced MCF-7 cell apoptosis, which was highly correlated with inactivation of cyclin D1/CDK4. In 2015, Fang et al. (2015) showed that calycosin promoted apoptosis of tumor cells MCF-7, possibly in part by reducing SIRT1 levels, thereby increasing p53 and cleaved caspase-3 expression to promote apoptosis. In 2015, Wei et al. (2015) reported that gambogic acid lysinate induced MCF-7 cell apoptosis in a dose-dependent manner by inhibiting SIRT1 protein expression levels and upregulating cleaved caspase-3 protein expression levels. In 2019, Cheng et al. (2019) indicated that icariin can significantly downregulate CDK2, CDK4, cyclin D1, and Bcl-2 and upregulate cleaved caspase-3 and PARP, thereby inducing apoptosis of the tamoxifen-resistant MCF-7/TAM BC cell line. In 2020, Yousuf et al. (2020) proposed that ellagic acid controlled cell proliferation and induced BC cell apoptosis by inhibiting CDK6. Moradi et al. (2020) also proposed in 2020 that flavonoid calycopterin can induce MDA-MB-231 cell apoptosis by increasing the caspase-3/8 expression. In addition, treatment with flavonoid calycopterin can also increase the ratio of Bax/Bcl-2.
Notch signaling can act as a therapeutic target to induce or resist cell apoptosis. When the Notch receptor is activated by DLL-1/2/3 and Jagged-1/2, the Notch intracellular domain (NIC) is released from the cell membrane. Then, the NIC translocates into the nucleus where it regulates the expression of target genes to induce a series of biochemical reactions. In 2021, Jiang et al. reported that quercetin could increase the expression of GAS5, Bax, and caspase-3 and decrease the expressions of Notch1, Jagged1, Hes1, and Bcl-2 in MCF-7 cells, suggesting that quercetin can induce BC cell apoptosis by the GAS5/Notch1 signaling pathway (Jiang et al., 2021). In 2019, a study by Lan et al. (2019) indicated that treatment with rhamnetin increased caspase-3/9 activity, upregulated p53 protein and miR-34a expression, and downregulated Notch-1 expression, suggesting that rhamnetin induced apoptosis of human BC cells through the miR-34a/Notch-1 signaling pathway. In 2021, Wang et al. (2021) reported that shikonin, a natural naphthoquinone isolated from Arnebiae radix, promoted the autoubiquitination and degradation of cIAP1 and cIAP2 to induce MDA-MB-231 cell apoptosis.
Abnormal expression of hedgehog ligands, overactivation of Smo proteins, and inappropriate disinhibition of Smo can lead to abnormal activation of the hedgehog pathway. Once the hedgehog pathway is activated, Gli transcription factors are transported into the nucleus in a full-length form and function as transcriptional activators to promote the abnormal expression of downstream VEGF, C-MYC, and other target genes, resulting in excessive cell proliferation and ultimately the occurrence of tumors. In 2020, Liu et al. (2020) showed that cordycepin induced apoptosis by inhibiting the hedgehog pathway, and this effect was associated with elevated levels of PUMA, CytoC, Fas, DR4/5, and cleaved caspase-3 and decreased levels of Bcl-2, XIAP, and PDGFR-α.
Extracts From Natural Product–Induced Apoptosis in BC
In this study, we summarized the effects and mechanisms of extracts from natural products on the apoptosis of BC (Table 2). In 2010, Tandrasasmita et al. (2010) proposed that Phaleria macrocarpa (Scheff.) Boerl extract markedly decreased the PI3K/AKT signaling pathway and resulted in MDA-MB-231 cell apoptosis. In 2012, Vaz et al. (2012) reported that the methanol extract of Suillus collinitus (Fr.) Kuntze remarkably upregulated the levels of p53, p21 and cleaved PARP and downregulated the levels of Bcl-2 and XIAP in MCF-7 cell lines, suggesting that S. collinitus–induced apoptosis was realized by mediating p53. In a 2015 study conducted by Hosseini et al., the dichloromethane extract of Scrophularia ningpoensis Hemsl. oxysepala upregulated the mRNA expression of caspase-3 and caspase-9 in MCF-7 cells. Further, the expression study of caspase-9 mRNA confirmed that the fractions triggered apoptosis via the intrinsic mitochondrial pathway (Hosseini et al., 2015). In 2015, Zheng et al. (2015) proposed that ethyl acetate was isolated from the seeds of Momordica cochinchinensis (Lour.) Spreng. can induce cell apoptosis, which was correlated with high expression of p53, Bax, Bak, and Bad, along with downregulation of NF-κB. In a 2015 study conducted by Petchsak et al., M. cochinchinensis (Lour.) Spreng. aril extract induced BC cell apoptosis by increasing the expression of the proapoptotic gene Bax and enhancing caspase-6/8/9 activity (Petchsak and Sripanidkulchai, 2015). In 2015, Chen et al. (2015a) reported that extraction of isoflavones from chickpea Cicer arietinum L. sprouts induced apoptosis in SKBR3 and MCF-7 cells by increasing the expression of Bax, caspase-7/9, p53, and p21, and decreasing Bcl-2 expression. In 2016, Foo et al. reported that Dillenia suffruticosa (Griff.) Martelli root extract induced MDA-MB-231 cell apoptosis via activation of proapoptotic JNK1 and downregulation of antiapoptotic ERK1 and Bcl-2, increasing the Bax/Bcl-2 ratio and initiating the mitochondrial apoptosis pathway (Foo et al., 2016). In 2017, Liu et al. (2017b) reported that Camellia sinensis (L.) Kuntze polyphenols induced chromatin condensation, MMP reduction, ROS increase, and caspase-3/9 activation in BC cells, which indicated that C. sinensis (L.) Kuntze polyphenols induced mitochondrial pathway–mediated apoptosis. In 2017, Kello et al. (2017) found that peel polyphenol extracts induced apoptosis by increasing intracellular oxidative stress, activating p38 MAPK, and inhibiting ERK1/2 and AKT signaling pathways. In 2018, Zhang et al. (2018b) isolated three flavonoids from Tephroseris kirilowii (Turcz. ex DC.) Holub (isorhamnetin, genkwanin, and acacetin), which suppressed cell growth and induced apoptosis in MDA-MB-231 cells by downregulating the PI3K/AKT/mTOR/p70S6K/ULK signaling pathway. In 2018, Lin et al. (2018) proposed that the ethanol extract of Antrodia cinnamomea induced MCF-7 cell apoptosis by elevating the expression of miR-21-5p, miR-26-5p, and miR-30-5p and decreasing SKP2 mRNA expression. In 2018, Chun et al. (2018) found that the sesquiterpene lactones-enriched fraction of Inula helenium L. induced apoptosis via suppression of signal transducers and activators of the STAT3 signaling pathway in MDA-MB-231 cells. In 2019, Majumder et al. (2019) proposed that Ricinus communis L. fruit extract can contribute to apoptosis in MCF-7 and MDA-MB-231 cells by promoting the attenuation of antiapoptotic Bcl-2 and the accumulation of proapoptotic Bax and caspase-7 and PARP cleavage. In 2019, Lee et al. (2019) reported that Fomes fomentarius (L.Fr.) Kick. ethanol extracts induced apoptosis by inhibiting the PI3K/AKT pathway and activating the caspase pathway. In 2019, Kim et al. (2019) reported that the proapoptotic effect of Toxicodendron vernicifluum (Stokes) F.A. Barkley stokes extract in MCF-7 cells was attributed to p53, p21, and the intrinsic mitochondrial cascade. In a 2019 study, Chaudhry et al. (2019) reported that Vitex agnus-castus L. hexane and dichloromethane extracts induced T47D cell apoptosis by activating external and internal pathways, and this effect was concomitant with activation of caspase-8/9 and -3/7, upregulation of Bax and downregulation of Bcl-2. Khan et al. showed in a study in 2021 that Phoenix dactylifera L. ethanol extracts induced apoptosis in TNBC MDA-MB-231 cells. This effect was related to the upregulation of p53, Bax, and cleaved caspase-3 expression and downregulation of Bcl-2 and AKT/mTOR pathways (Khan et al., 2021).
TABLE 2. Extracts from natural products induced apoptosis in breast cancer.
Conclusion
Through a systematic summary, we found that numerous monomers/extracts have an anti-BC capacity, and the mechanism is closely associated with apoptosis. The mechanism of agent-induced apoptosis predominantly involves the mitochondrial pathway, PIK3K/AKT, NF-κB, MAPK, JAK-STAT3, and other pathways. Therefore, identifying potential anti-BC drugs from natural products is one of the most effective strategies. However, there are still some problems, and further studies should be performed in the future.
First, >50% of the studies mentioned in this review were performed in vitro. As we know, drugs undergo four processes in vivo, including absorption, distribution, metabolism, and excretion, all of which affect the therapeutic effect of drugs. Many drugs are effective in vitro. However, they have little or no effect in vivo. Therefore, animal experiments should be conducted to further confirm the proapoptotic effects of natural agents. Moreover, there is a lack of toxicity studies and clinical data on the majority of the reported natural products. Therefore, the therapeutic effects, side effects, and toxicity of these drugs should be the focus on the future studies. More time is required before these natural products are used clinically. Furthermore, the evidence regarding the mechanism of certain natural products mentioned in our article to promote BC cell apoptosis is unclear and inadequate. Further, we can use diversified detection methods, such as CRISPR-Cas9, single-cell sequencing, and proteomic technology, to clarify the mechanism in detail, which will be conducive to the development and use of these natural products. Finally, most natural products still have flaws, such as low bioavailability, poor solubility, and poor selectivity, which interfere with their clinical application (Zhang et al., 2021a). Therefore, special processes can be considered to overcome these deficiencies. We can modify the structure of the compound. For example, polar groups can be joined to increase the solubility. Nanoparticle drug delivery systems for natural products can increase bioavailability and reduce toxicity to other organs.
In conclusion, we reviewed current studies on natural products that induced BC cell apoptosis and summarized the pro-apoptotic mechanisms. We hope that our review can provide direction in the search for candidate drugs derived from natural products to treat BC by inhibiting cell apoptosis.
Author Contributions
LY collected documents and wrote the manuscript. YC drew the mechanism figures. LZ and SL collected the documents. PL polished the language and revised the manuscript. XL conceived ideas, designed the structure of the manuscript and revised the manuscript. All authors read and approved the submitted version.
Funding
This project is supported by Natural Science Foundation of Chongqing (No. csct2020jcyj-msxmX0223), Technology Project of Chongqing Health and Family Planning Commission (No. 2019MSXM010), and Basic Research and Frontier Exploration Project of Yuzhong District of Chongqing (No. 20190102).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
Alshatwi, A. A., Subash-Babu, P., and Antonisamy, P. (2016). Violacein Induces Apoptosis in Human Breast Cancer Cells through up Regulation of BAX, P53 and Down Regulation of MDM2. Exp. Toxicol. Pathol. 68 (1), 89–97. doi:10.1016/j.etp.2015.10.002
Ateba, S. B., Mvondo, M. A., Ngeu, S. T., Tchoumtchoua, J., Awounfack, C. F., Njamen, D., et al. (2018). Natural Terpenoids against Female Breast Cancer: A 5-year Recent Research. Curr. Med. Chem. 25 (27), 3162–3213. doi:10.2174/0929867325666180214110932
Banafa, A. M., Roshan, S., Liu, Y. Y., Chen, H. J., Chen, M. J., Yang, G. X., et al. (2013). Fucoidan Induces G1 Phase Arrest and Apoptosis through Caspases-dependent Pathway and ROS Induction in Human Breast Cancer MCF-7 Cells. J. Huazhong Univ. Sci. Technolog Med. Sci. 33 (5), 717–724. doi:10.1007/s11596-013-1186-8
Benzina, S., Harquail, J., Jean, S., Beauregard, A. P., Colquhoun, C. D., Carroll, M., et al. (2015). Deoxypodophyllotoxin Isolated from Juniperus Communis Induces Apoptosis in Breast Cancer Cells. Anticancer Agents Med. Chem. 15 (1), 79–88. doi:10.2174/1871520614666140608150448
Binkley, J. M., Harris, S. R., Levangie, P. K., Pearl, M., Guglielmino, J., Kraus, V., et al. (2012). Patient Perspectives on Breast Cancer Treatment Side Effects and the Prospective Surveillance Model for Physical Rehabilitation for Women with Breast Cancer. Cancer 118 (8 Suppl. l), 2207–2216. doi:10.1002/cncr.27469
Chaudhry, G. E., Jan, R., Naveed Zafar, M., Mohammad, H., and Muhammad, T. S. T. (2019). Vitex Rotundifolia Fractions Induced Apoptosis in Human Breast Cancer T-47D Cell Line via Activation of Extrinsic and Intrinsic Pathway. Asian Pac. J. Cancer Prev. 20 (12), 3555–3562. doi:10.31557/APJCP.2019.20.12.3555
Chen, H., Ma, H. R., Gao, Y. H., Zhang, X., Habasi, M., Hu, R., et al. (2015a). Isoflavones Extracted from Chickpea Cicer Arietinum L. Sprouts Induce Mitochondria-dependent Apoptosis in Human Breast Cancer Cells. Phytother Res. 29 (2), 210–219. doi:10.1002/ptr.5241
Chen, J., Duan, Y., Zhang, X., Ye, Y., Ge, B., and Chen, J. (2015b). Genistein Induces Apoptosis by the Inactivation of the IGF-1R/p-Akt Signaling Pathway in MCF-7 Human Breast Cancer Cells. Food Funct. 6 (3), 995–1000. doi:10.1039/c4fo01141d
Chen, J., Lin, C., Yong, W., Ye, Y., and Huang, Z. (2015c). Calycosin and Genistein Induce Apoptosis by Inactivation of HOTAIR/p-Akt Signaling Pathway in Human Breast Cancer MCF-7 Cells. Cell Physiol Biochem 35 (2), 722–728. doi:10.1159/000369732
Chen, J., and Sun, L. (2012). Formononetin-induced Apoptosis by Activation of Ras/p38 Mitogen-Activated Protein Kinase in Estrogen Receptor-Positive Human Breast Cancer Cells. Horm. Metab. Res. 44 (13), 943–948. doi:10.1055/s-0032-1321818
Chen, M., Xiao, C., Jiang, W., Yang, W., Qin, Q., Tan, Q., et al. (2021). Capsaicin Inhibits Proliferation and Induces Apoptosis in Breast Cancer by Down-Regulating FBI-1-Mediated NF-Κb Pathway. Drug Des. Devel Ther. 15, 125–140. doi:10.2147/DDDT.S269901
Cheng, L., Shi, L., Wu, J., Zhou, X., Li, X., Sun, X., et al. (2018). A Hederagenin Saponin Isolated from Clematis Ganpiniana Induces Apoptosis in Breast Cancer Cells via the Mitochondrial Pathway. Oncol. Lett. 15 (2), 1737–1743. doi:10.3892/ol.2017.7494
Cheng, L., Xia, T. S., Wang, Y. F., Zhou, W., Liang, X. Q., Xue, J. Q., et al. (2014). The apoptotic effect of D Rhamnose β-hederin, a novel oleanane-type triterpenoid saponin on breast cancer cells. PLoS One 9 (6), e90848. doi:10.1371/journal.pone.0090848
Cheng, X., Tan, S., Duan, F., Yuan, Q., Li, Q., and Deng, G. (2019). Icariin Induces Apoptosis by Suppressing Autophagy in Tamoxifen-Resistant Breast Cancer Cell Line MCF-7/TAM. Breast Cancer 26 (6), 766–775. doi:10.1007/s12282-019-00980-5
Chun, J., Song, K., and Kim, Y. S. (2018). Sesquiterpene Lactones-Enriched Fraction of Inula Helenium L. Induces Apoptosis through Inhibition of Signal Transducers and Activators of Transcription 3 Signaling Pathway in MDA-MB-231 Breast Cancer Cells. Phytother Res. 32 (12), 2501–2509. doi:10.1002/ptr.6189
Fallahian, F., Aghaei, M., Abdolmohammadi, M. H., and Hamzeloo-Moghadam, M. (2015). Molecular Mechanism of Apoptosis Induction by Gaillardin, a Sesquiterpene Lactone, in Breast Cancer Cell Lines : Gaillardin-Induced Apoptosis in Breast Cancer Cell Lines. Cell Biol Toxicol 31 (6), 295–305. doi:10.1007/s10565-016-9312-6
Fan, X. W., Zang, Y., Xi, L., and Li, S. D. (2015). The Emodin Inducted Human Breast Cancer MCF-7cell Apoptosis and Activated JNK Signal Transduction Pathways. J. Chin. J. Surg. Oncol. 7 (06), 346–350.
Fang, K., Liu, J. C., Qu, M. L., and Chang, N. D. (2015). Calycosin Promotes Apoptosis of Breast Cancer Cells MCF-7 through Inhibiting SIRT1. J. Prog. Mod. Biomed. 15 (23), 4431–4434.
Feng, J. X., Chen, J. H., and Lin, Q. H. (2021). Saikosaponin D Inhibits Proliferation and Promotes Apoptosis in Breast Cancer Cells through Down-Regulating JAK2/STAT3 Pathway. J. J. Third Mil. Med. Univ. 43 (09), 852–857.
Feng, S. D., Wu, D., Yang, S. S., He, J. Q., Zhang, K. F., and Ling, H. Y. (2016). Effect of Arecoline on Proliferation and Apoptosis of MCF-7 Human Breast Cancer Cells. Zhongguo Ying Yong Sheng Li Xue Za Zhi 32 (4), 370–372. doi:10.13459/j.cnki.cjap.2016.04.021
Foo, J. B., Saiful Yazan, L., Tor, Y. S., Wibowo, A., Ismail, N., Armania, N., et al. (2016). Dillenia suffruticosa Dichloromethane Root Extract Induced Apoptosis towards MDA-MB-231 Triple-Negative Breast Cancer Cells. J. Ethnopharmacol 187, 195–204. doi:10.1016/j.jep.2016.04.048
Gao, S., Li, X., Ding, X., Qi, W., and Yang, Q. (2017). Cepharanthine Induces Autophagy, Apoptosis and Cell Cycle Arrest in Breast Cancer Cells. Cel Physiol Biochem 41 (4), 1633–1648. doi:10.1159/000471234
Gao, S., Sun, D., Wang, G., Zhang, J., Jiang, Y., Li, G., et al. (2016). Growth Inhibitory Effect of Paratocarpin E, a Prenylated Chalcone Isolated from Euphorbia Humifusa Wild., by Induction of Autophagy and Apoptosis in Human Breast Cancer Cells. Bioorg. Chem. 69, 121–128. doi:10.1016/j.bioorg.2016.10.005
Georgalas, I., Paraskevopoulos, T., Koutsandrea, C., Kardara, E., Malamos, P., Ladas, D., et al. (2015). Ophthalmic Metastasis of Breast Cancer and Ocular Side Effects from Breast Cancer Treatment and Management: Mini Review. Biomed. Res. Int. 2015, 574086. doi:10.1155/2015/574086
Han, B., Jiang, P., Liu, W., Xu, H., Li, Y., Li, Z., et al. (2018). Role of Daucosterol Linoleate on Breast Cancer: Studies on Apoptosis and Metastasis. J. Agric. Food Chem. 66 (24), 6031–6041. doi:10.1021/acs.jafc.8b01387
Han, Y. Y., Yang, J. F., Sun, Y., and Li, L. H. (2019). Parthenolide on Proliferation and Apoptosis of Breast Cancer. J. Northwest. J. Defense Med. 40 (04), 205–211.
Hassan, Z. K., Elamin, M. H., Omer, S. A., Daghestani, M. H., Al-Olayan, E. S., Elobeid, M. A., et al. (2014). Oleuropein Induces Apoptosis via the P53 Pathway in Breast Cancer Cells. Asian Pac. J. Cancer Prev. 14 (11), 6739–6742. doi:10.7314/apjcp.2013.14.11.6739
Hematpoor, A., Paydar, M., Liew, S. Y., Sivasothy, Y., Mohebali, N., Looi, C. Y., et al. (2018). Phenylpropanoids Isolated from Piper Sarmentosum Roxb. Induce Apoptosis in Breast Cancer Cells through Reactive Oxygen Species and Mitochondrial-dependent Pathways. Chem. Biol. Interact 279, 210–218. doi:10.1016/j.cbi.2017.11.014
Hong, Y., and Fan, D. (2019). Ginsenoside Rk1 Induces Cell Cycle Arrest and Apoptosis in MDA-MB-231 Triple Negative Breast Cancer Cells. Toxicology 418, 22–31. doi:10.1016/j.tox.2019.02.010
Hosseini, B. A., Pasdaran, A., Kazemi, T., Shanehbandi, D., Karami, H., Orangi, M., et al. (2015). Dichloromethane Fractions of Scrophularia Oxysepala Extract Induce Apoptosis in MCF-7 Human Breast Cancer Cells. Bosn J. Basic Med. Sci. 15 (1), 26–32. doi:10.17305/bjbms.2015.1.226
Hou, L. L., Xu, Q. J., Hu, G. Q., and Xie, S. Q. (2014). Fucoxanthin Induces Human MCF-7 Breast Cancer Cells Apoptosis via Endoplasmic Reticulum Pathway. J. Chin. Pharm. J. 49 (02), 117–120.
Hu, J., Zhang, H., Li, J., Jiang, X., Zhang, Y., Wu, Q., et al. (2020). ROCK1 Activation-Mediated Mitochondrial Translocation of Drp1 and Cofilin Are Required for Arnidiol-Induced Mitochondrial Fission and Apoptosis. J. Exp. Clin. Cancer Res. 39 (1), 37. doi:10.1186/s13046-020-01545-7
Hu, S., Huang, L., Meng, L., Sun, H., Zhang, W., and Xu, Y. (2015). Isorhamnetin Inhibits Cell Proliferation and Induces Apoptosis in Breast Cancer via Akt and Mitogen-activated P-rotein K-inase K-inase S-ignaling P-athways. Mol. Med. Rep. 12 (5), 6745–6751. doi:10.3892/mmr.2015.4269
Hu, S., Xu, Y., Meng, L., Huang, L., and Sun, H. (2018). Curcumin Inhibits Proliferation and Promotes Apoptosis of Breast Cancer Cells. Exp. Ther. Med. 16 (2), 1266–1272. doi:10.3892/etm.2018.6345
Huang, C., Chen, X., Guo, B., Huang, W., Shen, T., Sun, X., et al. (2012). Induction of Apoptosis by Icariside II through Extrinsic and Intrinsic Signaling Pathways in Human Breast Cancer MCF7 Cells. Biosci. Biotechnol. Biochem. 76 (7), 1322–1328. doi:10.1271/bbb.120077
Huang, W. C., Gu, P. Y., Fang, L. W., Huang, Y. L., Lin, C. F., Liou, C. J., et al. (2019). Sophoraflavanone G from Sophora Flavescens Induces Apoptosis in Triple-Negative Breast Cancer Cells. Phytomedicine 61, 152852. doi:10.1016/j.phymed.2019.152852
Jang, H., Ko, H., Song, K., and Kim, Y. S. (2019). A Sesquiterpenoid from Farfarae Flos Induces Apoptosis of MDA-MB-231 Human Breast Cancer Cells through Inhibition of JAK-STAT3 Signaling. Biomolecules 9 (7). doi:10.3390/biom9070278
Jia, S. H., Liu, L. N., and Yan, T. H. (2020). Mechanism of Apoptosis and Oxidative Stress in MCF–7 Cells Induced by Formononetin. J. West. China J. Pharm. Sci. 35 (04), 385–391.
Jiang, D. C., Jin, L., Chen, H. X., and Zhang, L. (2021). Quercetin Promotes Apoptosis of Breast Cancer Cells by Targeting GAS5/Notch1 Signaling Pathway. J. Chin. Pharmacol. Bull. 37 (05), 637–644.
Kawiak, A., and Lojkowska, E. (2016). Ramentaceone, a Naphthoquinone Derived from Drosera sp., Induces Apoptosis by Suppressing PI3K/Akt Signaling in Breast Cancer Cells. PLoS One 11 (2), e0147718. doi:10.1371/journal.pone.0147718
Kello, M., Kulikova, L., Vaskova, J., Nagyova, A., and Mojzis, J. (2017). Fruit Peel Polyphenolic Extract-Induced Apoptosis in Human Breast Cancer Cells Is Associated with ROS Production and Modulation of p38MAPK/Erk1/2 and the Akt Signaling Pathway. Nutr. Cancer 69 (6), 920–931. doi:10.1080/01635581.2017.1339819
Khan, M. A., Siddiqui, S., Ahmad, I., Singh, R., Mishra, D. P., Srivastava, A. N., et al. (2021). Phytochemicals from Ajwa Dates Pulp Extract Induce Apoptosis in Human Triple-Negative Breast Cancer by Inhibiting AKT/mTOR Pathway and Modulating Bcl-2 Family Proteins. Sci. Rep. 11 (1), 10322. doi:10.1038/s41598-021-89420-z
Khojasteh Poor, F., Keivan, M., Ramazii, M., Ghaedrahmati, F., Anbiyaiee, A., Panahandeh, S., et al. (2021). Mini Review: The FDA-Approved Prescription Drugs that Target the MAPK Signaling Pathway in Women with Breast Cancer. Breast Dis. 40 (2), 51–62. doi:10.3233/bd-201063
Kim, B. M., Kim, D. H., Park, J. H., Na, H. K., and Surh, Y. J. (2013). Ginsenoside Rg3 Induces Apoptosis of Human Breast Cancer (MDA-MB-231) Cells.. J. Cancer Prev. 18 (2), 177–185. doi:10.15430/jcp.2013.18.2.177
Kim, E. A., Jang, J. H., Lee, Y. H., Sung, E. G., Song, I. H., Kim, J. Y., et al. (2014). Dioscin Induces Caspase-independent Apoptosis through Activation of Apoptosis-Inducing Factor in Breast Cancer Cells. Apoptosis 19 (7), 1165–1175. doi:10.1007/s10495-014-0994-z
Kim, E. S., Jeong, C. S., and Moon, A. (2012). Genipin, a Constituent of Gardenia Jasminoides Ellis, Induces Apoptosis and Inhibits Invasion in MDA-MB-231 Breast Cancer Cells. Oncol. Rep. 27 (2), 567–572. doi:10.3892/or.2011.1508
Kim, M. S., Lee, C. W., Kim, J. H., Lee, J. C., and An, W. G. (2019). Extract of Rhus Verniciflua Stokes Induces P53-Mediated Apoptosis in MCF-7 Breast Cancer Cells. Evid. Based Complement. Alternat Med. 2019, 9407340. doi:10.1155/2019/9407340
Kim, S. H., Choo, G. S., Yoo, E. S., Woo, J. S., Lee, J. H., Han, S. H., et al. (2021). Silymarin Inhibits Proliferation of Human Breast Cancer Cells via Regulation of the MAPK Signaling Pathway and Induction of Apoptosis. Oncol. Lett. 21 (6), 492. doi:10.3892/ol.2021.12753
Kong, W., Li, C., Qi, Q., Shen, J., and Chang, K. (2019). Cardamonin Induces G2/M Arrest and Apoptosis via Activation of the JNK-FOXO3a Pathway in Breast Cancer Cells. Cell Biol Int 44, 177–188. doi:10.1002/cbin.11217
Kong, Y., Chen, J., Zhou, Z., Xia, H., Qiu, M. H., and Chen, C. (2014). Cucurbitacin E Induces Cell Cycle G2/M Phase Arrest and Apoptosis in Triple Negative Breast Cancer. PLoS One 9 (7), e103760. doi:10.1371/journal.pone.0103760
Kritsanawong, S., Innajak, S., Imoto, M., and Watanapokasin, R. (2016). Antiproliferative and Apoptosis Induction of α-mangostin in T47D Breast Cancer Cells. Int. J. Oncol. 48 (5), 2155–2165. doi:10.3892/ijo.2016.3399
Kushwaha, P. P., Singh, A. K., Prajapati, K. S., Shuaib, M., Fayez, S., Bringmann, G., et al. (2020). Induction of Apoptosis in Breast Cancer Cells by Naphthylisoquinoline Alkaloids. Toxicol. Appl. Pharmacol. 409, 115297. doi:10.1016/j.taap.2020.115297
Lai, Y. B., Wang, Y. Q., and Yao, Q. H. (2016). Effect of Tetramethylpyrazine on Breast Cancer MCF-7 Cell Apoptosis and The Underlying Mechanism. Zhejiang J. Integr. Traditional Chinese Western Med. 26 (02), 105–107.
Lan, L., Wang, Y., Pan, Z., Wang, B., Yue, Z., Jiang, Z., et al. (2019). Rhamnetin Induces Apoptosis in Human Breast Cancer Cells via the miR-34a/Notch-1 Signaling Pathway. Oncol. Lett. 17 (1), 676–682. doi:10.3892/ol.2018.9575
Lee, D., Yu, J. S., Ryoo, R., Kim, J.-C., Jang, T. S., Kang, K. S., et al. (2021). Pulveraven A from the Fruiting Bodies of Pulveroboletus Ravenelii Induces Apoptosis in Breast Cancer Cell via Extrinsic Apoptotic Signaling Pathway. J. Antibiot. 74, 752–757. doi:10.1038/s41429-021-00435-0
Lee, H. L., Lin, C. S., Kao, S. H., and Chou, M. C. (2017). Gallic Acid Induces G1 Phase Arrest and Apoptosis of Triple-Negative Breast Cancer Cell MDA-MB-231 via P38 Mitogen-Activated Protein Kinase/p21/p27 axis. Anticancer Drugs 28 (10), 1150–1156. doi:10.1097/CAD.0000000000000565
Lee, H. M., and Moon, A. (2016). Amygdalin Regulates Apoptosis and Adhesion in Hs578T Triple-Negative Breast Cancer Cells. Biomol. Ther. (Seoul) 24 (1), 62–66. doi:10.4062/biomolther.2015.172
Lee, S. O., Lee, M. H., Lee, K. R., Lee, E. O., and Lee, H. J. (2019). Fomes Fomentarius Ethanol Extract Exerts Inhibition of Cell Growth and Motility Induction of Apoptosis via Targeting AKT in Human Breast Cancer MDA-MB-231 Cells. Int. J. Mol. Sci. 20 (5). doi:10.3390/ijms20051147
Li, G., Zhou, J., Budhraja, A., Hu, X., Chen, Y., Cheng, Q., et al. (2015). Mitochondrial Translocation and Interaction of Cofilin and Drp1 Are Required for Erucin-Induced Mitochondrial Fission and Apoptosis. Oncotarget 6 (3), 1834–1849. doi:10.18632/oncotarget.2795
Li, G. B., Fu, R. Q., Shen, H. M., Zhou, J., Hu, X. Y., Liu, Y. X., et al. (2017a). Polyphyllin I Induces Mitophagic and Apoptotic Cell Death in Human Breast Cancer Cells by Increasing Mitochondrial PINK1 Levels. Oncotarget 8 (6), 10359–10374. doi:10.18632/oncotarget.14413
Li, H., Prever, L., Hirsch, E., and Gulluni, F. (2021). Targeting PI3K/AKT/mTOR Signaling Pathway in Breast Cancer. Cancers 13 (14), 3517. doi:10.3390/cancers13143517
Li, P., Tian, W., and Ma, X. (2014). Alpha-mangostin Inhibits Intracellular Fatty Acid Synthase and Induces Apoptosis in Breast Cancer Cells. Mol. Cancer 13, 138. doi:10.1186/1476-4598-13-138
Li, X. X., Wang, D. Q., Sui, C. G., Meng, F. D., Sun, S. L., Zheng, J., et al. (2020). Oleandrin Induces Apoptosis via Activating Endoplasmic Reticulum Stress in Breast Cancer Cells. Biomed. Pharmacother. 124, 109852. doi:10.1016/j.biopha.2020.109852
Li, Y., Li, D., Yuan, S., Wang, Z., Tang, F., Nie, R., et al. (2013). Embelin-induced MCF-7 Breast Cancer Cell Apoptosis and Blockade of MCF-7 Cells in the G2/M Phase via the Mitochondrial Pathway. Oncol. Lett. 5 (3), 1005–1009. doi:10.3892/ol.2012.1084
Li, Z. H., Gao, J., Hu, P. H., and Xiong, J. P. (2017b). Anticancer Effects of Liriodenine on the Cell Growth and Apoptosis of Human Breast Cancer MCF-7 Cells through the Upregulation of P53 Expression. Oncol. Lett. 14 (2), 1979–1984. doi:10.3892/ol.2017.6418
Liang, Z. J., Wan, Y., Zhu, D. D., Wang, M. X., Jiang, H. M., Huang, D. L., et al. (2021). Resveratrol Mediates the Apoptosis of Triple Negative Breast Cancer Cells by Reducing POLD1 Expression. Front. Oncol. 11, 569295. doi:10.3389/fonc.2021.569295
Liao, W. L., Lin, J. Y., Shieh, J. C., Yeh, H. F., Hsieh, Y. H., Cheng, Y. C., et al. (2019). Induction of G2/M Phase Arrest by Diosgenin via Activation of Chk1 Kinase and Cdc25C Regulatory Pathways to Promote Apoptosis in Human Breast Cancer Cells. Int. J. Mol. Sci. 21 (1). doi:10.3390/ijms21010172
Lin, Y. S., Lin, Y. Y., Yang, Y. H., Lin, C. L., Kuan, F. C., Lu, C. N., et al. (2018). Antrodia Cinnamomea Extract Inhibits the Proliferation of Tamoxifen-Resistant Breast Cancer Cells through Apoptosis and skp2/microRNAs Pathway. BMC Complement. Altern. Med. 18 (1), 152. doi:10.1186/s12906-018-2204-y
Liu, B. W., Zhang, B., Zhang, Y., and Feng, W. H. (2012). Apigenin Induces P53-dependent Apoptosis and G/M Arrest in Breast Cancer T47D Cells. J. Chin. J. Clin. Oncol. 39 (06), 315–317.
Liu, C., Qi, M., Li, L., Yuan, Y., Wu, X., and Fu, J. (2020). Natural Cordycepin Induces Apoptosis and Suppresses Metastasis in Breast Cancer Cells by Inhibiting the Hedgehog Pathway. Food Funct. 11 (3), 2107–2116. doi:10.1039/c9fo02879j
Liu, C., Zhang, K., Shen, H., Yao, X., Sun, Q., and Chen, G. (2018a). Necroptosis: A Novel Manner of Cell Death, Associated with Stroke (Review). Int. J. Mol. Med. 41 (2), 624–630. doi:10.3892/ijmm.2017.3279
Liu, D., You, P., Luo, Y., Yang, M., and Liu, Y. (2018b). Galangin Induces Apoptosis in MCF-7 Human Breast Cancer Cells through Mitochondrial Pathway and Phosphatidylinositol 3-Kinase/Akt Inhibition. Pharmacology 102 (1-2), 58–66. doi:10.1159/000489564
Liu, G., Liu, Z., Yan, Y., and Wang, H. (2017a). Effect of Fraxetin on Proliferation and Apoptosis in Breast Cancer Cells. Oncol. Lett. 14 (6), 7374–7378. doi:10.3892/ol.2017.7143
Liu, S. M., Ou, S. Y., and Huang, H. H. (2017b). Green tea Polyphenols Induce Cell Death in Breast Cancer MCF-7 Cells through Induction of Cell Cycle Arrest and Mitochondrial-Mediated Apoptosis. J. Zhejiang Univ. Sci. B 18 (2), 89–98. doi:10.1631/jzus.B1600022
Liu, Y., and Fan, D. (2018). Ginsenoside Rg5 Induces Apoptosis and Autophagy via the Inhibition of the PI3K/Akt Pathway against Breast Cancer in a Mouse Model. Food Funct. 9 (11), 5513–5527. doi:10.1039/c8fo01122b
Liu, Z. H., Yang, C. X., Zhang, L., Yang, C. Y., and Xu, X. Q. (2019). Baicalein, as a Prooxidant, Triggers Mitochondrial Apoptosis in MCF-7 Human Breast Cancer Cells through Mobilization of Intracellular Copper and Reactive Oxygen Species Generation. Onco Targets Ther. 12, 10749–10761. doi:10.2147/OTT.S222819
Looi, C. Y., Arya, A., Cheah, F. K., Muharram, B., Leong, K. H., Mohamad, K., et al. (2013). Induction of Apoptosis in Human Breast Cancer Cells via Caspase Pathway by Vernodalin Isolated from Centratherum Anthelminticum (L.) Seeds. PLoS One 8 (2), e56643. doi:10.1371/journal.pone.0056643
Ma, C. L., Zhang, B. L., and Zhang, C. H. (2020). Effects of Curcuma on Proliferation and Apoptosis of Breast Cancer Cells and JAK2/STAT3 Signaling Pathway. J. J. Chin. Oncol. 26 (07), 616–620.
Ma, Q., Chen, J., Xiong, S., and Li, G. L. (2021). Effects of Dehydrocostuslactone on the Apoptosis of Human Breast Cancer SK- BR- 3 Cells and its Mechanism. J. Traditional Chin. Drug Res. Clin. Pharmacol. 32 (02), 200–207.
Ma, Y. P., and Sun, S. R. (2014). Effects of Ursolic Acid on Cell Apoptosis in MDA-MB-231 Cells and its Mechanisms. J. J. Liaoning Univ. Traditional Chin. Med. 16 (08), 59–62.
Majumder, M., Debnath, S., Gajbhiye, R. L., Saikia, R., Gogoi, B., Samanta, S. K., et al. (2019). Ricinus communis L. Fruit Extract Inhibits Migration/invasion, Induces Apoptosis in Breast Cancer Cells and Arrests Tumor Progression In Vivo. Sci. Rep. 9 (1), 14493. doi:10.1038/s41598-019-50769-x
Miricescu, D., Totan, A., Stanescu-Spinu, I. I., Badoiu, S. C., Stefani, C., and Greabu, M. (2020). PI3K/AKT/mTOR Signaling Pathway in Breast Cancer: From Molecular Landscape to Clinical Aspects. Int. J. Mol. Sci. 22 (1). doi:10.3390/ijms22010173
Mohammad, R. M., Muqbil, I., Lowe, L., Yedjou, C., Hsu, H. Y., Lin, L. T., et al. (2015). Broad Targeting of Resistance to Apoptosis in Cancer. Semin. Cancer Biol. 35 Suppl (Suppl. l), S78–s103. doi:10.1016/j.semcancer.2015.03.001
Moradi, M., Gholipour, H., Sepehri, H., Attari, F., Delphi, L., Arefian, E., et al. (2020). Flavonoid Calycopterin Triggers Apoptosis in Triple-Negative and ER-Positive Human Breast Cancer Cells through Activating Different Patterns of Gene Expression. Naunyn Schmiedebergs Arch. Pharmacol. 393 (11), 2145–2156. doi:10.1007/s00210-020-01917-y
N, B., Chandrashekar, K. R., Prabhu, A., and Rekha, P. D. (2019). Tetrandrine Isolated from Cyclea Peltata Induces Cytotoxicity and Apoptosis through ROS and Caspase Pathways in Breast and Pancreatic Cancer Cells. In Vitro Cel Dev Biol Anim 55 (5), 331–340. doi:10.1007/s11626-019-00332-9
Nasimian, A., Farzaneh, P., Tamanoi, F., and Bathaie, S. Z. (2020). Cytosolic and Mitochondrial ROS Production Resulted in Apoptosis Induction in Breast Cancer Cells Treated with Crocin: The Role of FOXO3a, PTEN and AKT Signaling. Biochem. Pharmacol. 177, 113999. doi:10.1016/j.bcp.2020.113999
Nguyen, L. T., Lee, Y. H., Sharma, A. R., Park, J. B., Jagga, S., Sharma, G., et al. (2017). Quercetin Induces Apoptosis and Cell Cycle Arrest in Triple-Negative Breast Cancer Cells through Modulation of Foxo3a Activity. Korean J. Physiol. Pharmacol. 21 (2), 205–213. doi:10.4196/kjpp.2017.21.2.205
Nøhr-Nielsen, A., Bagger, S. O., Brünner, N., Stenvang, J., and Lund, T. M. (2020). Pharmacodynamic Modelling Reveals Synergistic Interaction between Docetaxel and SCO-101 in a Docetaxel-Resistant Triple Negative Breast Cancer Cell Line. Eur. J. Pharm. Sci. 148, 105315. doi:10.1016/j.ejps.2020.105315
Pal, S., and Rakshit, T. (2021). Folate-Functionalized DNA Origami for Targeted Delivery of Doxorubicin to Triple-Negative Breast Cancer. Front. Chem. 9, 721105. doi:10.3389/fchem.2021.721105
Parton, M., Dowsett, M., and Smith, I. (2001). Studies of Apoptosis in Breast Cancer. Bmj 322 (7301), 1528–1532. doi:10.1136/bmj.322.7301.1528
Patel, P. B., and Thakkar, V. R. (2014). L-carvone Induces P53, Caspase 3 Mediated Apoptosis and Inhibits the Migration of Breast Cancer Cell Lines. Nutr. Cancer 66 (3), 453–462. doi:10.1080/01635581.2014.884230
Paul, S., Sengupta, S., Bandyopadhyay, T. K., and Bhattacharyya, A. (2012). Stevioside Induced ROS-Mediated Apoptosis through Mitochondrial Pathway in Human Breast Cancer Cell Line MCF-7. Nutr. Cancer 64 (7), 1087–1094. doi:10.1080/01635581.2012.712735
Pei, J. S., Liu, C. C., Hsu, Y. N., Lin, L. L., Wang, S. C., Chung, J. G., et al. (2012). Amentoflavone Induces Cell-Cycle Arrest and Apoptosis in MCF-7 Human Breast Cancer Cells via Mitochondria-dependent Pathway. In Vivo 26 (6), 963–970.
Peng, M., Zhai, H., Feng, Y. H., and Xin, L. W. (2016). Studies on Mechanisms of Rg3 Inducing Apoptosis through PI3K/Akt Mediating MGBA in Breast Cancer Cells. J. J. Liaoning Med. Univ. 37 (03), 114–115.
Pereyra-Vergara, F., Olivares-Corichi, I. M., Perez-Ruiz, A. G., Luna-Arias, J. P., and García-Sánchez, J. R. (2020). Apoptosis Induced by (−)-Epicatechin in Human Breast Cancer Cells Is Mediated by Reactive Oxygen Species. Molecules 25 (5). doi:10.3390/molecules25051020
Petchsak, P., and Sripanidkulchai, B. (2015). Momordica Cochinchinensis Aril Extract Induced Apoptosis in Human MCF-7 Breast Cancer Cells. Asian Pac. J. Cancer Prev. 16 (13), 5507–5513. doi:10.7314/apjcp.2015.16.13.5507
Qian, X. L., Pan, Y. H., Huang, Q. Y., Shi, Y. B., Huang, Q. Y., Hu, Z. Z., et al. (2019). Caveolin-1: a Multifaceted Driver of Breast Cancer Progression and its Application in Clinical Treatment. Onco Targets Ther. 12, 1539–1552. doi:10.2147/ott.S191317
Qiu, J., Zhang, T., Zhu, X., Yang, C., Wang, Y., Zhou, N., et al. (2019). Hyperoside Induces Breast Cancer Cells Apoptosis via ROS-Mediated NF-Κb Signaling Pathway. Int. J. Mol. Sci. 21 (1). doi:10.3390/ijms21010131
Rajabi, S., Maresca, M., Yumashev, A. V., Choopani, R., and Hajimehdipoor, H. (2021). The Most Competent Plant-Derived Natural Products for Targeting Apoptosis in Cancer Therapy. Biomolecules 11 (4). doi:10.3390/biom11040534
Rajput, S., Kumar, B. N., Dey, K. K., Pal, I., Parekh, A., and Mandal, M. (2013). Molecular Targeting of Akt by Thymoquinone Promotes G(1) Arrest through Translation Inhibition of Cyclin D1 and Induces Apoptosis in Breast Cancer Cells. Life Sci. 93 (21), 783–790. doi:10.1016/j.lfs.2013.09.009
Ranganathan, S., Halagowder, D., and Sivasithambaram, N. D. (2015). Quercetin Suppresses Twist to Induce Apoptosis in MCF-7 Breast Cancer Cells. PLoS One 10 (10), e0141370. doi:10.1371/journal.pone.0141370
Razak, N. A., Abu, N., Ho, W. Y., Zamberi, N. R., Tan, S. W., Alitheen, N. B., et al. (2019). Cytotoxicity of Eupatorin in MCF-7 and MDA-MB-231 Human Breast Cancer Cells via Cell Cycle Arrest, Anti-angiogenesis and Induction of Apoptosis. Sci. Rep. 9 (1), 1514. doi:10.1038/s41598-018-37796-w
Ren, L., Li, Z., Dai, C., Zhao, D., Wang, Y., Ma, C., et al. (2018). Chrysophanol Inhibits Proliferation and Induces Apoptosis through NF-κB/cyclin D1 and NF-κB/Bcl-2 Signaling cascade in Breast Cancer Cell Lines. Mol. Med. Rep. 17 (3), 4376–4382. doi:10.3892/mmr.2018.8443
Roos, W. P., and Kaina, B. (2013). DNA Damage-Induced Cell Death: from Specific DNA Lesions to the DNA Damage Response and Apoptosis. Cancer Lett. 332 (2), 237–248. doi:10.1016/j.canlet.2012.01.007
Rosas-González, V. C., Téllez-Bañuelos, M. C., Hernández-Flores, G., Bravo-Cuellar, A., Aguilar-Lemarroy, A., Jave-Suárez, L. F., et al. (2020). Differential Effects of Alliin and Allicin on Apoptosis and Senescence in Luminal A and Triple-Negative Breast Cancer: Caspase, ΔΨm, and Pro-apoptotic Gene Involvement. Fundam. Clin. Pharmacol. 34 (6), 671–686. doi:10.1111/fcp.12559
Seo, H. S., Ku, J. M., Choi, H. S., Woo, J. K., Jang, B. H., Shin, Y. C., et al. (2014). Induction of Caspase-dependent Apoptosis by Apigenin by Inhibiting STAT3 Signaling in HER2-Overexpressing MDA-MB-453 Breast Cancer Cells. Anticancer Res. 34 (6), 2869–2882.
Shao, H., Ma, J., Guo, T., and Hu, R. (2014). Triptolide Induces Apoptosis of Breast Cancer Cells via a Mechanism Associated with the Wnt/β-Catenin Signaling Pathway. Exp. Ther. Med. 8 (2), 505–508. doi:10.3892/etm.2014.1729
Sharma, G., Kar, S., Palit, S., and Das, P. K. (2012). 18β-glycyrrhetinic Acid Induces Apoptosis through Modulation of Akt/FOXO3a/Bim Pathway in Human Breast Cancer MCF-7 Cells. J. Cel Physiol 227 (5), 1923–1931. doi:10.1002/jcp.22920
Shen, J., Zeng, L., Pan, L., Yuan, S., Wu, M., and Kong, X. (2018). Tetramethylpyrazine Regulates Breast Cancer Cell Viability, Migration, Invasion and Apoptosis by Affecting the Activity of Akt and Caspase-3. Oncol. Lett. 15 (4), 4557–4563. doi:10.3892/ol.2018.7851
Shen, L.-w., Jiang, X.-x., Li, Z.-q., Li, J., Wang, M., Jia, G.-f., et al. (2021). Cepharanthine Sensitizes Human Triple Negative Breast Cancer Cells to Chemotherapeutic Agent Epirubicin via Inducing Cofilin Oxidation-Mediated Mitochondrial Fission and Apoptosis. Acta Pharmacol. Sin. doi:10.1038/s41401-021-00715-3
Shimanuki, Y., Shimomura, A., Yoshimura, K., Terakado, H., and Shimizu, C. (2021). Are Platinum Drugs Ineffective for Triple-Negative Breast Cancer with Residual Invasive Disease after Neoadjuvant Chemotherapy? Jco 39, 3521–3522. doi:10.1200/jco.21.01757
Shrestha, S., Sorolla, A., Fromont, J., Blancafort, P., and Flematti, G. R. (2018). Crambescidin 800, Isolated from the Marine Sponge Monanchora Viridis, Induces Cell Cycle Arrest and Apoptosis in Triple-Negative Breast Cancer Cells. Mar. Drugs 16 (2). doi:10.3390/md16020053
Shrivastava, S., Kulkarni, P., Thummuri, D., Jeengar, M. K., Naidu, V. G., Alvala, M., et al. (2014). Piperlongumine, an Alkaloid Causes Inhibition of PI3 K/Akt/mTOR Signaling axis to Induce Caspase-dependent Apoptosis in Human Triple-Negative Breast Cancer Cells. Apoptosis 19 (7), 1148–1164. doi:10.1007/s10495-014-0991-2
Siao, A. C., Hou, C. W., Kao, Y. H., and Jeng, K. C. (2015). Effect of Sesamin on Apoptosis and Cell Cycle Arrest in Human Breast Cancer Mcf-7 Cells. Asian Pac. J. Cancer Prev. 16 (9), 3779–3783. doi:10.7314/apjcp.2015.16.9.3779
Sindhu, R. K., Verma, R., Salgotra, T., Rahman, M. H., Shah, M., Akter, R., et al. (2021). Impacting the Remedial Potential of Nano Delivery-Based Flavonoids for Breast Cancer Treatment. Molecules 26 (17), 5163. doi:10.3390/molecules26175163
Sp, N., Kang, D. Y., Lee, J.-M., Bae, S. W., and Jang, K.-J. (2021). Potential Antitumor Effects of 6-Gingerol in P53-dependent Mitochondrial Apoptosis and Inhibition of Tumor Sphere Formation in Breast Cancer Cells. Ijms 22 (9), 4660. doi:10.3390/ijms22094660
Su, P., Ahmad, B., Zou, K., and Zou, L. (2020). β-Elemene Enhances the Chemotherapeutic Effect of 5-Fluorouracil in Triple-Negative Breast Cancer via PI3K/AKT, RAF-MEK-ErK, and NF-Κb Signaling Pathways. Onco Targets Ther. 13, 5207–5222. doi:10.2147/ott.S242820
Sultan, A. S., Marie, M. A., and Sheweita, S. A. (2018). Novel Mechanism of Cannabidiol-Induced Apoptosis in Breast Cancer Cell Lines. Breast 41, 34–41. doi:10.1016/j.breast.2018.06.009
Sun, X. D., Liu, X. E., and Huang, D. S. (2012). Curcumin Induces Apoptosis of Triple-Negative Breast Cancer Cells by Inhibition of EGFR Expression. Mol. Med. Rep. 6 (6), 1267–1270. doi:10.3892/mmr.2012.1103
Sun, X., Yu, M. W., Ma, X. M., and Zhang, G. L. (2018). In Vitro and In Vivo Study of the Regulation of Fisetin in PI3K/Akt/mTOR Pathway to Induce Apoptosis of Breast Cancer Cells,” in The 15th National Conference of Integrated Traditional Chinese and Western Medicine oncology).2
Sung, H., Ferlay, J., Siegel, R. L., Laversanne, M., Soerjomataram, I., Jemal, A., et al. (2021). Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 71 (3), 209–249. doi:10.3322/caac.21660
Suraweera, C. D., Hinds, M. G., and Kvansakul, M. (2020). Poxviral Strategies to Overcome Host Cell Apoptosis. Pathogens 10 (1). doi:10.3390/pathogens10010006
Takeshima, M., Ono, M., Higuchi, T., Chen, C., Hara, T., and Nakano, S. (2014). Anti-proliferative and Apoptosis-Inducing Activity of Lycopene against Three Subtypes of Human Breast Cancer Cell Lines. Cancer Sci. 105 (3), 252–257. doi:10.1111/cas.12349
Tandrasasmita, O. M., Lee, J. S., Baek, S. H., and Tjandrawinata, R. R. (2010). Induction of Cellular Apoptosis in Human Breast Cancer by DLBS1425, a Phaleria Macrocarpa Compound Extract, via Down-Regulation of PI3-Kinase/AKT Pathway. Cancer Biol. Ther. 10 (8), 814–823. doi:10.4161/cbt.10.8.13085
Tian, J., Duan, Y. X., Bei, C. Y., and Chen, J. (2013). Calycosin Induces Apoptosis by Upregulation of RASD1 in Human Breast Cancer Cells MCF-7. Horm. Metab. Res. 45 (8), 593–598. doi:10.1055/s-0033-1341510
Vaz, J. A., Ferreira, I. C., Tavares, C., Almeida, G. M., Martins, A., and Helena Vasconcelos, M. (2012). Suillus Collinitus Methanolic Extract Increases P53 Expression and Causes Cell Cycle Arrest and Apoptosis in a Breast Cancer Cell Line. Food Chem. 135 (2), 596–602. doi:10.1016/j.foodchem.2012.04.127
Vazhappilly, C. G., Hodeify, R., Siddiqui, S. S., Laham, A. J., Menon, V., El-Awady, R., et al. (2021). Natural Compound Catechol Induces DNA Damage, Apoptosis, and G1 Cell Cycle Arrest in Breast Cancer Cells. Phytother Res. 35 (4), 2185–2199. doi:10.1002/ptr.6970
Viau, C. M., Moura, D. J., Facundo, V. A., and Saffi, J. (2014). The Natural Triterpene 3β,6β,16β-Trihydroxy-Lup-20(29)-Ene Obtained from the Flowers of Combretum Leprosum Induces Apoptosis in MCF-7 Breast Cancer Cells. BMC Complement. Altern. Med. 14, 280. doi:10.1186/1472-6882-14-280
Wang, A., Liu, J., Yang, Y., Chen, Z., Gao, C., Wang, Z., et al. (2021). Shikonin Promotes Ubiquitination and Degradation of cIAP1/2-Mediated Apoptosis and Necrosis in Triple Negative Breast Cancer Cells. Chin. Med. 16 (1), 16. doi:10.1186/s13020-021-00426-1
Wang, C. J., Sheng, Y., Zhou, Q., and He, H. X. (2020). Anti-proliferation and Pro-apoptotic Activities of Diosmetin on MCF-7 Cells via Mitochondrial Apoptosis Pathway. J. Traditional Chin. Drug Res. Clin. Pharmacol. 31 (02), 149–155.
Wang, D., Zhang, Y., Lu, J., Wang, Y., Wang, J., Meng, Q., et al. (2016). Cordycepin, a Natural Antineoplastic Agent, Induces Apoptosis of Breast Cancer Cells via Caspase-dependent Pathways. Nat. Prod. Commun. 11 (1), 63–68. doi:10.1177/1934578x1601100119
Wang, H., Lu, C., Ma, W., and Mao, J. (2013a). Genistein-induced Apoptosis in Breast Cancer MDA-MB-231 Cells. J. Chin. J. Breast Dis. 7 (05), 322–328.
Wang, J. S., Ren, T. N., and Xi, T. (2012). Ursolic Acid Induces Apoptosis by Suppressing the Expression of FoxM1 in MCF-7 Human Breast Cancer Cells. Med. Oncol. 29 (1), 10–15. doi:10.1007/s12032-010-9777-8
Wang, M., Shu, Z. J., Wang, Y., and Peng, W. (2017). Stachydrine Hydrochloride Inhibits Proliferation and Induces Apoptosis of Breast Cancer Cells via Inhibition of Akt and ERK Pathways. Am. J. Transl Res. 9 (4), 1834–1844.
Wang, S., Zhong, Z., Wan, J., Tan, W., Wu, G., Chen, M., et al. (2013b). Oridonin Induces Apoptosis, Inhibits Migration and Invasion on Highly-Metastatic Human Breast Cancer Cells. Am. J. Chin. Med. 41 (1), 177–196. doi:10.1142/S0192415X13500134
Wei, J., Li, K. J., Wei, J. B., and Lv, C. P. (2015). Influence of Gambogic Acid Lysinate in Proliferation and Apoptosis in Breast Cancer MCF 7 Cells and its Mechanism. J. J. Jilin Univ. (Medical Sci. Edition) 41 (03), 476–480.
Wei, T., Xiaojun, X., and Peilong, C. (2020). Magnoflorine Improves Sensitivity to Doxorubicin (DOX) of Breast Cancer Cells via Inducing Apoptosis and Autophagy through AKT/mTOR and P38 Signaling Pathways. Biomed. Pharmacother. 121, 109139. doi:10.1016/j.biopha.2019.109139
Wu, G. L., Peng, J. Y., and Yu, X. P. (2018a). “Delphintin Induces Apoptosis and Molecular Mechanism of HER-2 Positive Breast Cancer Cells,” in The 11th Special Nutrition Conference of Chinese Nutrition Society.1
Wu, G. S., Lu, J. J., Guo, J. J., Li, Y. B., Tan, W., Dang, Y. Y., et al. (2012). Ganoderic Acid DM, a Natural Triterpenoid, Induces DNA Damage, G1 Cell Cycle Arrest and Apoptosis in Human Breast Cancer Cells. Fitoterapia 83 (2), 408–414. doi:10.1016/j.fitote.2011.12.004
Wu, Y. Z., Zeng, Y., Zheng, K. S., and Wu, L. B. (2018b). Salviaflaside Induces the Breast Cancer Cell Apoptosis by Activating Endoplasmic Reticulum Stress. J. Chin. J. Surg. Integrated Traditional West. Med. 24 (06), 749–753.
Xie, J., Xu, Y., Huang, X., Chen, Y., Fu, J., Xi, M., et al. (2015). Berberine-induced Apoptosis in Human Breast Cancer Cells Is Mediated by Reactive Oxygen Species Generation and Mitochondrial-Related Apoptotic Pathway. Tumour Biol. 36 (2), 1279–1288. doi:10.1007/s13277-014-2754-7
Xie, Z. Z., Li, M. M., Deng, P. F., Wang, S., Wang, L., Lu, X. P., et al. (2017). Paris Saponin-Induced Autophagy Promotes Breast Cancer Cell Apoptosis via the Akt/mTOR Signaling Pathway. Chem. Biol. Interact 264, 1–9. doi:10.1016/j.cbi.2017.01.004
Xu, Y., Fang, R., Shao, J., and Cai, Z. (2021). Erianin Induces Triple-Negative Breast Cancer Cells Apoptosis by Activating PI3K/Akt Pathway. Biosci. Rep. 41 (6). doi:10.1042/BSR20210093
Yan, W., Ma, X., Zhao, X., and Zhang, S. (2018). Baicalein Induces Apoptosis and Autophagy of Breast Cancer Cells via Inhibiting PI3K/AKT Pathway In Vivo and Vitro. Drug Des. Devel Ther. 12, 3961–3972. doi:10.2147/DDDT.S181939
Yeh, H. T., Tsai, Y. S., Chen, M. S., Li, Y. Z., Lin, W. C., Lee, Y. R., et al. (2019). Flavopereirine Induces Cell Cycle Arrest and Apoptosis via the AKT/p38 MAPK/ERK1/2 Signaling Pathway in Human Breast Cancer Cells. Eur. J. Pharmacol. 863, 172658. doi:10.1016/j.ejphar.2019.172658
Yousuf, M., Shamsi, A., Khan, P., Shahbaaz, M., AlAjmi, M. F., Hussain, A., et al. (2020). Ellagic Acid Controls Cell Proliferation and Induces Apoptosis in Breast Cancer Cells via Inhibition of Cyclin-dependent Kinase 6. Int. J. Mol. Sci. 21 (10). doi:10.3390/ijms21103526
Yu, L., Strandberg, L., and Lenardo, M. J. (2008). The Selectivity of Autophagy and its Role in Cell Death and Survival. Autophagy 4 (5), 567–573. doi:10.4161/auto.5902
Yu, Q., Wang, W. S., and Zhu, B. B. (2020). Effect of Avicularin on the Apoptosis, Cell Cycle and PI3K/AKT Signaling Pathway in Human Breast Cancer MDA-MB-231 Cells. J. Cent. South Pharm. 18 (01), 48–52.
Zhai, J. W., Gao, C., Ma, W. D., Wang, W., Yao, L. P., Xia, X. X., et al. (2016). Geraniin Induces Apoptosis of Human Breast Cancer Cells MCF-7 via ROS-Mediated Stimulation of P38 MAPK. Toxicol. Mech. Methods 26 (5), 311–318. doi:10.3109/15376516.2016.1139025
Zhang, H., Xu, H. L., Wang, Y. C., Lu, Z. Y., Yu, X. F., and Sui, D. Y. (2018a). 20(S)-Protopanaxadiol-Induced Apoptosis in MCF-7 Breast Cancer Cell Line through the Inhibition of PI3K/AKT/mTOR Signaling Pathway. Int. J. Mol. Sci. 19 (4). doi:10.3390/ijms19041053
Zhang, H. W., Hu, J. J., Fu, R. Q., Liu, X., Zhang, Y. H., Li, J., et al. (2018b). Flavonoids Inhibit Cell Proliferation and Induce Apoptosis and Autophagy through Downregulation of PI3Kγ Mediated PI3K/AKT/mTOR/p70S6K/ULK Signaling Pathway in Human Breast Cancer Cells. Sci. Rep. 8 (1), 11255. doi:10.1038/s41598-018-29308-7
Zhang, H., and Zhu, L. (2016). Osthole Induce Human Breast Cancer Cells Lines MCF-7 Apoptosis by Activating P53 Signaling Pathway. J. Chin. J. Mod. Appl. Pharm. 33 (05), 547–551.
Zhang, P., Wang, Z. X., Zhang, Y. F., and Chen, Q. L. (2021a). Advances in the Research of Natural Products Anti-breast Tumor Nanometer Drug Delivery System. J. Chin. Pharm. J. 56(06), 429–435.
Zhang, R., Kang, R., and Tang, D. (2021b). The STING1 Network Regulates Autophagy and Cell Death. Signal. Transduct Target. Ther. 6 (1), 208. doi:10.1038/s41392-021-00613-4
Zhang, X., Luo, W., Zhao, W., Lu, J., and Chen, X. (2015a). Isocryptotanshinone Induced Apoptosis and Activated MAPK Signaling in Human Breast Cancer MCF-7 Cells. J. Breast Cancer 18 (2), 112–118. doi:10.4048/jbc.2015.18.2.112
Zhang, Y., Hao, C., wang, B. G., and Xing, Z. B. (2017). The Mechanism of Fangchinoline in Inducing the Apoptosis of MDA-MB-231 Human Breast Cancer Cells. J. Oncol. Prog. 15 (03), 250–254.
Zhang, Y. J., Qian, L., and Chen, C. J. (2015b). Effect of Berberine on Proliferation and Apoptosis of MCF-7 Cells. J. Acta Universitatis Medicinalis Anhui 50 (09), 1276–1280.
Zhao, M. Z., Zhang, L., Zhou, D., and Ding, Q. Q. (2019). Kaempferol Regulates PI3K/AKT/GSK-3β Signaling Pathway and Promotes Apoptosis of Human Inflammatory Breast Cancer Cell Line SUM190. J. J. Guangxi Med. Univ. 36 (06), 872–877.
Zhao, Y., Jing, Z., Lv, J., Zhang, Z., Lin, J., Cao, X., et al. (2017). Berberine Activates Caspase-9/cytochrome C-Mediated Apoptosis to Suppress Triple-Negative Breast Cancer Cells In Vitro and In Vivo. Biomed. Pharmacother. 95, 18–24. doi:10.1016/j.biopha.2017.08.045
Zheng, L., Zhang, Y., Liu, Y., Yang, X. O., and Zhan, Y. (2015). Momordica Cochinchinensis Spreng. Seed Extract Suppresses Breast Cancer Growth by Inducing Cell Cycle Arrest and Apoptosis. Mol. Med. Rep. 12 (4), 6300–6310. doi:10.3892/mmr.2015.4186
Zhou, J., Luo, Y. H., Wang, J. R., Lu, B. B., Wang, K. M., and Tian, Y. (2013). Gambogenic Acid Induction of Apoptosis in a Breast Cancer Cell Line. Asian Pac. J. Cancer Prev. 14 (12), 7601–7605. doi:10.7314/apjcp.2013.14.12.7601
Zhu, L., and Xue, L. (2019). Kaempferol Suppresses Proliferation and Induces Cell Cycle Arrest, Apoptosis, and DNA Damage in Breast Cancer Cells. Oncol. Res. 27 (6), 629–634. doi:10.3727/096504018X15228018559434
Zhu, X., Wang, K., Zhang, K., Zhu, L., and Zhou, F. (2014). Ziyuglycoside II Induces Cell Cycle Arrest and Apoptosis through Activation of ROS/JNK Pathway in Human Breast Cancer Cells. Toxicol. Lett. 227 (1), 65–73. doi:10.1016/j.toxlet.2014.03.015
Keywords: breast cancer, apoptosis, natural products, monomer, mechanism
Citation: Yuan L, Cai Y, Zhang L, Liu S, Li P and Li X (2022) Promoting Apoptosis, a Promising Way to Treat Breast Cancer With Natural Products: A Comprehensive Review. Front. Pharmacol. 12:801662. doi: 10.3389/fphar.2021.801662
Received: 25 October 2021; Accepted: 13 December 2021;
Published: 28 January 2022.
Edited by:
Wei Peng, Chengdu University of Traditional Chinese Medicine, ChinaReviewed by:
Guobing Li, The Third Military Medical University, ChinaYunhui Chen, Chengdu University of Traditional Chinese Medicine, China
Copyright © 2022 Yuan, Cai, Zhang, Liu, Li and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xiaoli Li, plum181181@126.com; Pan Li, 756248601@qq.com