Qicai Xiao1,2†
Wangshu Zhu3†Wei Feng1†
Su Seong Lee4Albert Wingnang Leung5Jun Shen3*
Liqian Gao1*
Chuanshan Xu2,6,7*- 1School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Guangzhou, China
- 2School of Chinese Medicine, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong
- 3Department of Radiology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China
- 4Institute of Bioengineering and Nanotechnology, Singapore, Singapore
- 5Division of Chinese Medicine, School of Professional and Continuing Education, The University of Hong Kong, Pokfulam, Hong Kong
- 6Key Laboratory of Molecular Target and Clinical Pharmacology, State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China
- 7Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China
Background: Cancer has become a major disease endangering human health around the world. Conventional chemotherapy suffers from many side effects including pain, cardiotoxicity, hepatotoxicity, and renal toxicity. This review aims to describe a natural product of resveratrol as a chemoprotective and synergistic agent in the modulation of cancer chemotherapy.
Methods: The publications were identified by comprehensive searching of SciFinder, PubMed, Web of Science, and our own reference library. Search terms included combinations of “resveratrol,” “cancer,” “natural products,” “chemotherapy,” and “side effects.” Selection of material focused on resveratrol reducing the side effects on cancer chemotherapy.
Results: Thirty one references were referred in this review to outline resveratrol as a potent chemoprotective and synergistic agent in cancer chemotherapy, including 22 papers for describing the chemoprotective effects, and 9 papers for illustrating the synergistic effects.
Conclusion: This study provides a systematic summary of resveratrol serving as a potent chemoprotective and synergistic agent to reduce the associated-side effects and enhance the therapeutic outcomes in cancer chemotherapy. Further studies in terms of resveratrol on a large amount of preclinical tests and clinical trials are highly demanded.
Introduction
Cancer, also known as malignant tumor, is a major public health problem around the world, not only brings unutterable pains to patients, but also leads to heavy economic burden to the families and society (Chen et al., 2016; Siegel et al., 2016, 2017). The global incidence of cancer is increasing yearly, and the total mortality has exceeded many other diseases, making it become a great killer to human health. It is reported that there was about 90.5 million cancer patients in 2015, and almost 14.1 million new cases occur each year, excluding skin cancer but melanoma (Bernard and Christopher, 2014; Vos et al., 2016). The global cancer death was around 8.8 million in 2015, which is almost 1 in 6 of all global deaths (Vos et al., 2016). In spite of tremendous efforts having been paid to improve this situation and find novel treatments, such as, radiotherapy, surgery, and immunotherapy, chemotherapy is up to now still the major approach used in clinic. However, chemotherapy often suffers from many side effects, such as cardiotoxicity, hepatotoxicity, renal toxicity and, easy recurrence and metastasis (Monsuez et al., 2010; Shukla et al., 2011).
Natural products have been one of the most important and essential sources in drug discovery and development (Shen, 2015; Wang et al., 2016; Xiao et al., 2018). For years, humans have relied on natural products and/or natural herbal formulations for the maintenance of health, prevention of diseases, and improvement of mental and physical health. Particularly, many studies have demonstrated that some natural products in combination with chemotherapeutic agents can play chemoprotective and/or synergistic effects in terms of reducing cancer chemotherapy-associated side effects and enhancing the therapeutic efficacy (Cragg and Pezzuto, 2016).
Resveratrol (RES, 3,5,4′-trihydroxy-trans-stilbene) is a naturally occurring polyphenol presented in lots of dietary substances, such as grapes, wine, nuts, berries and many other human foods (Figure 1) (Berman et al., 2017). It often occurs as a white powder with moderate water solubility (0.03 mg/mL). The molecular skeleton of RES is composed by two phenolic rings, one with a para hydroxyl group, and the other with an ortho double hydroxyl groups. The two benzene rings are connected through a double bond that affords isomers with cis and trans configuration. Usually, the most referred RES is the trans isomer, which is the most abundant and biologically active compound. It is reported that the total content of RES is around 50–100 μg/g in fresh grape skin, 5.1 μg/g in boiled peanuts, 0.31 μg/g in peanut buffer and 0.98–1.80 mg/L in red wine (Burns et al., 2002; Cal et al., 2003). Besides, a large amount of RES is also found in Itadori plants and tea, and the commercial grape juice contains about 4 mg/L of RES (Table 1) (Burns et al., 2002).
Figure 1. Resources of RES and its potent biological activities.
Table 1. Contents of RES in different substances.
Resveratrol as a natural polyphenol, it has been confirmed to have a broad range of biological activities, including anti-inflammatory, anti-oxidant, anti-viral, anti-fungal and anti-aging effects (Baur et al., 2006; Carter et al., 2014; Kotecha et al., 2016; Chedea et al., 2017; Nawaz et al., 2017). The broad biological activities of RES is primarily ascribed to its unique structure character with multiple phenolic hydroxyl groups, as polyphenol compounds are capable of scavenging free radicals to form more stable molecules with less toxicity than the original radicals (Frémont, 2000). In 1997, a pioneering work initiated by Jiang et al. revealed that RES could inhibit the cellular effects involving the three stages of carcinogenesis, including tumor initiation, promotion and progression, arousing the impetus and interest in the investigation of RES (Jang et al., 1997).
Numerous studies have shown that RES possessed chemoprotective effects, such as cardioprotective activity and neuroprotective activity (Cho et al., 2017; Riba et al., 2017; Sarubbo et al., 2017; Cai et al., 2018). Upon co-administration with chemotherapeutic agents, RES could decrease the associated-side effects while enhance the therapeutic efficacy concomitant with cancer chemotherapy. Currently, a few papers summarized the therapeutic benefits and chemopreventive effects of RES, ranging from autoimmune diseases to neoplastic diseases (Aziz et al., 2003; Kotecha et al., 2016; Berman et al., 2017; de Brito Monteiro et al., 2017; Ko et al., 2017). To the best of our knowledge, there is up to now no review article focusing on RES as a combinational agent to reduce the associated-side effects and enhance the therapeutic efficacy in cancer chemotherapy. Therefore, this work represents the first survey and summary of RES as a chemoprotective and synergistic agent in cancer chemotherapy. In addition, the mechanisms of RES-medicated cancer therapy, potential limitations and future perspectives of RES in clinical applications are also presented and discussed.
Materials and Methods
Search Strategy and Information Sources
This review was in line with recommendations from the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. The publications were identified by comprehensive searching of SciFinder, PubMed, Web of Science, and our own reference library. Search terms included combinations of “resveratrol,” “cancer,” “natural products,” “chemotherapy,” and “side effects.”
Study Selection, Data Collection, and Exclusion/Inclusion Criteria
Selection of material was limited to papers published in English language. All of the publications were at least checked by two investigators. Patents, books, dissertations, and abstracts of conferences were excluded. Also the studies with regard only to the therapeutic effects of RES such as anti-aging, anti-fungal, anti-inflammatory, and anti-viral activities were excluded. Studies related to RES on reducing chemotherapy-induced side effects, the chemoprotective effects of RES against external factors such as carcinogens-induced damages, and the synergistic effects of RES to enhance the therapeutic efficacy are the inclusion criteria.
Results
Using the search strategies mentioned above afforded 7,678 records, and among which 699 records were in Chinese. After applying the exclusion criteria, 7,647 publications were removed, which includes; (a) 702 records, such as conferences, patents, dissertations and books, (b) 5,526 records were not correlated to cancer chemotherapy, (c) 675 records did not refer to the side effects in cancer chemotherapy, and (d) 45 records did not meet the inclusion criteria. A flow chart (Figure 2) illustrates the screening process and study selection.
Figure 2. The flow chart of publications screening process.
RES as a Chemoprotective Agent in Cancer Chemotherapy
The adverse effects induced by chemotherapeutic agents are always the obstacles for their broad application in clinic. As a naturally occurring multifunctional molecule, RES has been reported to be capable of performing protective effects to reduce the associated-side effects induced by chemotherapeutic drugs.
Cardio-Protective Effects in Cancer Chemotherapy
Cardiotoxicity is a common side effect induced by chemotherapeutic agents in cancer chemotherapy. The generally used ANT, such as Dox or daunorubicin, usually brings severely cardiotoxic effects including myocarditis, arrhythmias, dilated cardiomyopathy, and congestive heart failure (Chatterjee et al., 2010). It is accepted that the production of free radicals and oxidative stress are involved in cardiotoxicity, and Dox was found to enhance the formation of ROS in heart tissues (Šimůnek et al., 2009; Deavall et al., 2012). Sheu et al. (2015) investigated the anti-oxidizing effects of 4 different kinds of antioxidants including RES. It was found that the intracellular ROS levels were significantly decreased after being co-treated with the antioxidants and Dox. In addition, the SOD levels that involved in eliminating ROS were increased. Among these tested antioxidants, RES was found to be the best one to neutralize ROS. Therefore, RES can be used as an efficient supplement to reduce the cardiotoxicity in Dox-mediated cancer chemotherapy. Besides, some other studies showed that the adverse effects of ANT might be ascribed to the metabolites of ANT that is generated by a two electron reduction, such as DOXol, a reduced metabolite from Dox, which is more cardiotoxic than Dox (Hanna et al., 2014; Piska et al., 2017). The reason for the high cardiotoxicity of DOXol is that it acts as a potent inhibitor of Ca2+, Mg2+, and Na+/K+-ATPases, and Ca2+ is the link between electric stimulation and cell contraction. Disruption of the calcium regulation system is considered to be responsible for DOXol cardiotoxicity (Piska et al., 2017). In general, the generation of ANT metabolites is catalyzed by cytosolic enzymes of CBR and AKR. Therefore, the inhibitors for CBR and AKR are believed to have cardioprotective effects (Huang et al., 2010; Zhou et al., 2015). Ito et al. (2013) reported that RES and its analogs (4′-methoxy, 5-methoxy and 4′-amino) could bind CBR1 to inhibit its activity, thus reducing the cardiotoxicity of Dox.
In addition, another kind of traditional anticancer drug named As2O3 is mainly used for the treatment of acute APL, hematologic malignancies and some solid tumors (Waxman and Anderson, 2001; Emadi and Gore, 2010). The adverse events of As2O3 include cardiotoxicity, electrocardiogram abnormalities, nephrotoxicity, hepatotoxicity, APL differentiation syndrome, and sudden death (Westervelt et al., 2001; Vuky et al., 2002; Emadi and Gore, 2010). Just as ANT-induced side effects, the primary pathogenic mechanism of As2O3 is correlated with the oxidative stress, which engenders the dysfunction of antioxidant defense system, thus leading to oxidative damage to cellular macromolecules due to the generation of free radicals (Emadi and Gore, 2010; Wang et al., 2012). Zhao et al. (2008) reported that prior treatment with RES (3 mg/kg) 1 h before As2O3 administration could protect against As2O3-induced cardiotoxicity, and attenuate myocardial injury, DNA fragmentation and oxidative damage.
Nephroprotective Effects in Cancer Chemotherapy
It is believed that ingestion of arsenic, both from water supplies and foods could cause renal damage, and chronic arsenic exposure could cause degenerative changes in kidneys (Liu et al., 2000). Moreover, As2O3 treatment for relapsed or refractory APL and MM were also reported to cause renal injury, such as elevated serum creatinine, blood urea nitrogen and protein urea concentration levels in clinical studies (Zhang et al., 2000). Yu et al. (2013) found that RES could facilitate the methylation and excretion of ascetic, thus significantly attenuated As2O3-induced arsenic accumulation, structural abnormalities and arsenic-related toxicity in kidney.
Hepaticprotective Effects in Cancer Chemotherapy
Liver plays a significant role in clearing and transforming chemicals, which is susceptible to the toxicity from these toxic agents. Besides cardiotoxicity and nephrotoxicity, it was also reported that As2O3 could cause hepatotoxicity which is associated with the generation of ROS. Zhang et al. (2013) reported that RES could attenuate As2O3-induced oxidative stress, decrease the arsenic accumulation in liver, and increase the activities of antioxidant enzymes, thus preventing As2O3-induced hepatotoxicity. In addition, several other studies reported that RES could protect acetaminophen-induced and pyrogallol-induced hepatotoxicity through its potent antioxidant activities (Şener et al., 2006; Upadhyay et al., 2008).
Gastrointestinal Protective Effects in Cancer Chemotherapy
The adverse effects in gastrointestinal tract are also present in chemotherapeutic drug mediated therapy, including anorexia, nausea, vomiting, constipation and diarrhea. Aspirin is a typical NASID widely used for the treatment of inflammation, fever and pain for more than one century. It functions through inhibiting the COX - an intracellular enzyme that catalyzes the rate-limiting step in the metabolic conversion of arachidonic acid to PGs and related eicosanoids (Patrono et al., 2005). Recent studies indicated that aspirin can be used in cancer prevention, particularly for reducing the risk of colorectal neoplasms (Chan et al., 2007; Thun et al., 2012; Thorat and Cuzick, 2013). However, the primary side effects in aspirin-mediated therapy are the gastric ulceration, which is due to the inhibition of COX-1. Dey et al. (2009) reported that a lower dose of RES (2 mg/kg) has the capability to protect gastric mucosa from NSAID-induced side effects, while a higher dose of RES (10 mg/kg) demonstrated a contraindicative effect, which might be resulted from the balance level between COX-1 and eNOS. To further ameliorate the side effects caused by aspirin, Zhu et al. (2015) constructed the RAH, which acted as a prodrug with the capability of releasing aspirin and RES simultaneously. It was found that most of RAH was transited out from stomach, while parts of the intact RAH were detected in the mouse colon tissue collected at 1 and 2 h after administration. The stability tests of RAH in cancer cells revealed that RAH was hydrolyzed into deacetyl-RAH and subsequently decomposed to release RES and aspirin over 24 h of incubation, suggesting that RAH is able to bear the acidic environment in stomach, avoid enzymatic hydrolysis in small intestine, and incorporate into the colon tissue to perform its antitumor activity. Another study initiated by Ko et al. (2016) showed that pretreatment wistar rats with whole grape juice that contains large amounts of RES could induce gastric emptying, improve the tubular dilatation and tubular cell vacuolization in renal tubules, thus bringing beneficial effects in preventing cisplatin-induced gastrointestinal tract disorders.
Protective Effects in UVR-Induced Skin Cancer
Skin serves lots of essential functions including protection from environmental stressors and infections. Furthermore, it also provides immunological surveillance against germs, allergens, and irritants attempting to enter the body (Di Meglio et al., 2011; Draelos, 2012). UVR can induce cell death through an apoptotic pathway, demonstrating certain therapeutic potential (Ji et al., 2015). However, UVR exposure is also regarded as one of the dominant causes for skin cancer (65–90%), in addition to the genetic and environmental factors (Bowden, 2004; Lucas et al., 2008). A large number of studies indicated that RES is able to protect against UVR-induced skin cancer via modulating the proteins that are involved in apoptosis (Reagan-Shaw et al., 2004; Aziz et al., 2005a; Ndiaye et al., 2011). Jang et al. (1997) revealed that topical application of RES could afford substantially protective effects against chemically induced skin carcinogenesis in CD-1 mice. Afaq et al. (2003) reported that topical application of RES could inhibit UV-B-induced skin edema and cause a significant decrease in UV-B-mediated hydrogen peroxide production and the infiltration of leukocytes in SKH-1 hairless mice. It is reported that long term topical application of RES, both pre-treatment and post-treatment, could inhibit the tumor incidence and delay in the onset of tumorigenesis, (Aziz et al., 2005b) while the short term topical application of RES could lead to a marked inhibition of cellular proliferation and phosphorylation of surviving (Aziz et al., 2005a). Additionally, a few studies showed that some cell cycle regulatory molecules, inhibiting factors of apoptotic proteins, and cell signaling pathways under RES-mediated chemoprotective effects are also involved against the adverse effects of UVR-induced photocarcinogenesis (Adhami et al., 2003; Reagan-Shaw et al., 2004).
Protective Effects Against Carcinogenic Substances-Induced Damage
In addition to the chemoprotective effects during cancer chemotherapy, RES can also exert its protective effects against the toxicity induced by carcinogenic substances. For instance, Revel et al. (2003) found that RES (50 mg/kg/week) could protect the lung from DNA damage and apoptosis that is resulted from the carcinogen of benzo[a]pyrene. Tessitore et al. (2000) found that upon administration of RES (200 mg/kg/day), the number of aberrant crypt foci in azoxymethane-induced colon carcinogenesis in rats was reduced. Tang et al. (2009) found that RES treatment could partially prevent carbon tetrachloride-induced acute liver damage. Additionally, in a DMBA-induced mammary carcinogenesis model in rats, dietary administration of RES had indeed no effects on tumor volume but produced striking reductions in the incidence and multiplicity, and thus extended the latency period in tumor development (Banerjee et al., 2002).
RES as a Synergistic Agent in Cancer Chemotherapy
RES modulates multiple pathways involved in cell cycle, apoptosis and inflammation. In addition to the chemopreventive and chemoprotective effects, RES also demonstrates potent anticancer activity (Sarkar et al., 2009). It is known that a single treatment often demonstrates weak activity, incomplete efficiency, and drug-resistance. The combination therapy recently developed through simultaneously combining more than two drugs, often brings better therapeutic outcomes.
Estrogens as natural hormones, are mediated by ERs. Exposure to estrogens has been recognized as a major risk for a variety of cancers, especially for breast cancer and other estrogen-mediated cancers (Henderson and Feigelson, 2000; Cavalieri and Rogan, 2014). The major cause for this observation is due to the formation of estrogen-DNA adducts that initiate tumorigenesis (Pruthi et al., 2012). It was found by Zahid et al. (2007) that NAcCys and RES are efficient inhibitors for the formation of estrogen-DNA adducts. The further study showed that upon treatment of MCF-10F cells with RES and NAcCys simultaneously, the formed estrogen-DNA adducts decreased more than those treated by the individual compound alone, and in the meantime the tumor initiation process is more efficiently disrupted (Zahid et al., 2011). Wu et al. (2004) found that RES can enhance the anti-tumor effect of 5-FU on murine hepatoma model in vitro through inducing the S phase arrest of H22 cells. A similar study initiated by Dun et al. (2015) also showed that RES could enhance the anti-tumor efficacy of 5-FU by inducing S-phase arrest both in vitro and in vivo.
Action of RES alone or in combination with ROSC-a CDK inhibitor, on cell cycle progression in human HL-60 leukemia cells was studied by Komina and W
sierska-Gądek (2008). A striking synergistic effect was observed after a combined treatment for 24 h and followed by sequential post-incubation for 48 h in the presence of RES. The G(1) cell population was increased up to 80% at a fourfold lower dose of ROSC with the addition of RES (Komina and Wsierska-Gądek, 2008).
In another study, Casanova and his co-workers investigated the combined action of RES with MEL, a well-known alkylating agent used for breast cancer therapy (Casanova et al., 2012). It was found that RES could be able to enhance the antitumor effects of MEL in MCF-7 and MDA-MB-231 cells. Interestingly, sequential treatment with RES followed by MEL yielded more cytotoxic effects than that treatment with MEL followed by RES. This effect may be related to the ability of RES to sensitize MCF-7 cells and MDA-MB-231 cells to MEL induced apoptosis. Similarly, Jazirehi and Bonavida (2004) reported that RES could sensitize NHL and MM cell lines to paclitaxel-mediated apoptosis, thus enhancing the antitumor efficacy of paclitaxel.
Rapamycin and its derivatives are potent inhibitors of dysregulated mTORC1 which can inhibit the proliferation of numerous tumor cell lines and tumor models. It was observed by He et al. that under combination with RES, the rapamycin-induced AKT phosphorylation was significantly decreased, and the antitumor activity of rapamycin in breast cancer cell lines was enhanced, suggesting that RES could assist rapamycin to increase the therapeutic efficacy (He et al., 2011).
Additionally, in another example, Lee et al. (2013) investigated the efficacy of the combined action of RES and clofarabine in malignant mesothelioma MSTO-211H cells. By calculating the CI, it was found that this combined treatment could produce a strong synergistic antiproliferative effect in MSTO-211H cells. RES was speculated to participate in the PI3K/AKT signaling pathway through reducing the content of Sp1, and the synergistic antitumor effect might be partly through the inhibition of AKT phosphorylation and the suppression of Sp1 activation.
Mechanisms for RES-Medicated Cancer Therapy
As a naturally occurring small molecule, RES has been shown to be capable of mediating cancer therapy via targeting multiple pathways involving cancer initiation, promotion and progression (Elshaer et al., 2018). Cancer initiation is the first phase in cancer development, and a critical biomarker for this event is the elevated level of estrogen-DNA adducts in tissue, which indicates a high risk of cancer, such as in the etiology of breast cancer and prostate cancer (Cavalieri and Rogan, 2010; Zahid et al., 2011; Pruthi et al., 2012). RES can inhibit activating enzymes such as CYP19 (aromatase) and CYP1B1 (a kind of cytochrome P450 enzyme), and induce the expression of detoxification enzyme of NQO1 (NAD(P)H:quinone oxidoreductase 1), thus blocking the formation of estrogen-DNA adducts to protect against estrogen-initiated cancer (Figure 3). The synergistic effect of RES-mediated chemotherapy is also partly attributed to the interfering action to cancer initiation. In addition, RES-induced cell sensitization and the participation of RES in the modulation of cell cycle, especially in S –phase, also play significant roles for its synergistic effects (Jazirehi and Bonavida, 2004; He et al., 2011; Casanova et al., 2012; Lee et al., 2013).
Figure 3. A simplified pathway for estrogens-induced cancer formation and RES-interfered cancer initiation.
RES is capable of inhibiting angiogenesis and metastasis through its interaction with multiple molecular targets. Kundu and Surh (2008) summarized the potential molecular targets of RES, and the mechanisms for RES-mediated cancer therapy modified from Kundu and Surh are shown in Figure 4 (Kundu and Surh, 2008). Blockade of angiogenic and metastatic process of cancer progression and reduction of the resistance of chemotherapy suggest the chemotherapeutic potential of RES. The chemopreventive potential of RES is reflected by its capability of blocking the activation of various carcinogens and/or to stimulate their detoxification, to avert oxidative damage to the target cells, to decrease inflammatory responses, and to reduce proliferation of cancer cells. The chemoprotective effects of RES are indicated by its anti-oxidizing property for scavenging ROS and improving the activities of some anti-oxidizing enzymes. RES is capable of activating NF-κB (nuclear factor κB) and SIRTI that are the major regulators for inflammatory response, and inhibiting some critical cytokines such as pro-inflammatory molecules of IL-1β, TNFα and IL-6, and oxidoreductase such as CBR, AKR and COXs. Besides, RES-mediated chemoprotection can also be achieved by reducing the expression of EMMPRIN-an important regulator for the synthesis of matrix metalloproteinase (MMP) to transport metal ions (Liu et al., 2016; Xiao et al., 2016). Overall, numerous mechanisms are involved for contributing to RES’s activity against cancerous and precancerous cells, and more studies and clinical trials are needed to examine RES’s efficacy in cancer therapy.
Figure 4. Potential mechanisms for RES-medicated chemotherapy, chemoprevention and chemoprotection.
Discussion and Future Perspective
In spite of tremendous efforts having been spent in searching efficient cures for cancer, cancer is still one of the greatest killers to human life. The incidence of cancer is rapidly increasing, and the number of cancer-related deaths is predicted to be double in the next 50 years. Although cancer chemotherapy is still currently one of the most frequently used treatment to combat cancer, it can only improve the overall survival of patients, while the quality of life is decreased. Moreover, chemotherapy often brings risks of chemo-resistance and easy recurrence as well as a variety of side effects including cardiotoxicity, nephrotoxicity and gastrointestinal toxicity. Due to the heterogeneity of cancer, it is also difficult to find a specific target for cancer therapy. As a consequence, the combinational treatment with multiple targets is regarded as one of the most promising approach to defeat cancer.
Natural products as one of the important resources in drug research and development, demonstrate a broad range of biological activities for the prevention, protection and treatment of different diseases. RES as a natural polyphenol is widely distributed in many types of foods. Using RES for the treatment and prevention of various diseases, especially for cancers, are extensively investigated. It has been proved that RES is able to interact with multiple molecular and cellular targets in cancer. The current associated data, both in vitro and in vivo, showed positive results in chemoprotective as well as synergistic aspects, suggesting that RES has great potential in the management of cancer chemotherapy. The lack of side effects is probably attributed to the low or moderate doses of RES that would be rapidly metabolized to the safe glucoronate and other analogs. In addition to investigations with high doses of RES in similar experiments, it is also imperative to perform some associated clinical trials needed for verifying these promising results. However, as searched from the database of human clinical studies on website of Clinical Trials.gov, there are a total of 151 records. Most of these trials are related to evaluate the safety, bioavailability, pharmacokinetics and tolerability of RES. Only a small amount of studies are focused on investigating the efficacy of RES in certain types of cancers. Up to now, there are no completed or ongoing clinical trials of RES in combination with other anticancer drugs for reducing the associated-side effects and enhancing the therapeutic outcomes in cancer chemotherapy. Numerous studies are primarily focused on the in vitro and in vivo animal experiments. It is encouraging that researchers can get some useful information and learn lessons from previous clinical trials while designing new trials, which will hopefully lead to better results.
Additionally, due to the low bioavailability of RES, further modification and optimization of RES for finding improved analogs with high bioavailability and good specificity are extremely important. For example, HTS has been used to screen and identify the specific and targeting peptide ligands against different cancer cells or disease biomarkers. If targeting peptides could be conjugated to RES against the expected cancer cells or the important proteins of interest, it is expected that it could greatly improve the efficacy of RES but lower down the side effects (Gray and Brown, 2013; Gao et al., 2016; Jee et al., 2016; Ong et al., 2017).
Conclusion
To sum up, RES has been found to be capable of modulating cancer therapy through targeting multiple molecular and signal pathways. It can reduce the associated-side effects in cancer chemotherapy, such as cardiotoxicity, hepatotoxicity, renal toxicity, gastrointestinal toxicity, UVR-induced skin cancer, and carcinogens-induced injuries. RES is meanwhile capable of enhancing the outcomes by in combination with other chemotherapeutic drugs. These promising results will motivate researchers to perform more studies on RES, including further clinical trials, detailed mechanism investigations, and developing new derivatives with improved properties on enhancing the chemoprotective and therapeutic effects.
Author Contributions
QX searched relative articles, created the outline and drafted the manuscript. WZ and WF assisted in searching relative articles and drafting the manuscript. SL and AL re-checked the relative articles and revised the manuscript. JS, LG and CX supervised the manuscript writing and revised the manuscript.
Funding
This work was supported by the National Natural Science Foundation of China (Grant Nos. 31741030, 81571739, and 21877130), Innovation and Technology Fund of Shenzhen (JCYJ20170818164356675, JCYJ20170818164838252, and JCYJ20170307165459562), Natural Science Foundation of Guangdong Province (2018A030313510), and Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme (2017). We also acknowledge the funding support from the Institute of Bioengineering and Nanotechnology (Biomedical Research Council, Agency for Science, Technology and Research, Singapore).
Conflict of Interest Statement
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.
Abbreviations
5-FU, 5-fluorouracil; AKR, aldo-keto reductases; AKT, protein kinase B; ANT, anthracycline antibiotics; APL, promyelocytic leukemia; CBR, carbonyl reductases; CDK, cyclin-dependent kinases; CI, combination index; COX, cyclooxygenase; CYP19, a kind of aromatase; CYP1B1, a kind of cytochrome P450 enzyme; DMBA, 7,12-dimethylbenz[a]anthracene; Dox, doxorubicin; DOXol, doxorubicinol; EMMPRIN, extracellular matrix metalloproteinase inducer; eNOS, endothelial nitric oxide synthase; ERs, estrogen receptors; HTS, high through-put screening; MEL, melphalan; MM, multiple myeloma; MMP, matrix metalloproteinase; mTORC1, mammalian target of rapamycin complex-1; NAcCys, N-acetylcysteine; NASID, non-steroidal antiinflammatory drug; NHL, non-Hodgkin’s lymphoma; NQO1, (NAD(P)H:quinone oxidoreductase 1); PGs, prostaglandins; PI3K, phosphatidylinositol-3-kinase; RAH, RES-aspirin hybrid; RES, resveratrol; ROS, reactive oxygen species; ROSC, roscovitine; SIRT1, sirtuin (silent mating type information regulation 2 homolog) 1; SOD, superoxide dismutase; Sp1, specificity protein 1; UVR, ultraviolet radiation.
References
Adhami, V. M., Afaq, F., and Ahmad, N. (2003). Suppression of ultraviolet B exposure-mediated activation of NF-κB in normal human keratinocytes by resveratrol. Neoplasia 5, 74–82. doi: 10.1016/S1476-5586(03)80019-2
Afaq, F., Adhami, V. M., and Ahmad, N. (2003). Prevention of short-term ultraviolet B radiation-mediated damages by resveratrol in SKH-1 hairless mice? Toxicol. Appl. Pharmacol. 186, 28–37. doi: 10.1016/S0041-008X(02)00014-5
Aziz, M. H., Afaq, F., and Ahmad, N. (2005a). Prevention of ultraviolet-B radiation damage by resveratrol in mouse skin is mediated via modulation in survivin II. Photochem. Photobiol. 81, 25–31.
Aziz, M. H., Reagan-Shaw, S., Wu, J., Longley, B. J., and Ahmad, N. (2005b). Chemoprevention of skin cancer by grape constituent resveratrol: relevance to human disease? FASEB J. 19, 1193–1195.
Aziz, M. H., Kumar, R., and Ahmad, N. (2003). Cancer chemoprevention by resveratrol: in vitro and in vivo studies and the underlying mechanisms. Int. J. Oncol. 23, 17–28. doi: 10.3892/ijo.23.1.17
Banerjee, S., Bueso-Ramos, C., and Aggarwal, B. B. (2002). Suppression of 7,12-dimethylbenz(a)anthracene-induced mammary carcinogenesis in rats by resveratrol: role of nuclear factor-kappaB, cyclooxygenase 2, and matrix metalloprotease 9. Cancer Res. 62, 4945–4954.
Baur, J. A., Pearson, K. J., Price, N. L., Jamieson, H. A., Lerin, C., Kalra, A., et al. (2006). Resveratrol improves health and survival of mice on a high-calorie diet. Nature 444, 337–342. doi: 10.1038/nature05354
Berman, A. Y., Motechin, R. A., Wiesenfeld, M. Y., and Holz, M. K. (2017). The therapeutic potential of resveratrol: a review of clinical trials. NPJ Precis. Oncol. 1:35. doi: 10.1038/s41698-017-0038-6
Bernard, W. S., and Christopher, P. W. (2014). World Cancer Report 2014. Geneva: World Health Organization.
Bowden, G. T. (2004). Prevention of non-melanoma skin cancer by targeting ultraviolet-B-light signalling. Nat. Rev. Cancer 4, 23–35. doi: 10.1038/nrc1253
Burns, J., Yokota, T., Ashihara, H., Lean, M. E., and Crozier, A. (2002). Plant foods and herbal sources of resveratrol. J. Agric. Food Chem. 50, 3337–3340. doi: 10.1021/jf0112973
Cai, J., Liu, W., Lu, F., Kong, W., Zhou, X., Miao, P., et al. (2018). Resveratrol attenuates neurological deficit and neuroinflammation following intracerebral hemorrhage. Exp. Ther. Med. 15, 4131–4138. doi: 10.3892/etm.2018.5938
Cal, C., Garban, H., Jazirehi, A., Yeh, C., Mizutani, Y., and Bonavida, B. (2003). Resveratrol and cancer: chemoprevention, apoptosis, and chemoimmunosensitizing activities. Curr. Med. Chem. Anti Cancer Agents 3, 77–93. doi: 10.2174/1568011033353443
Carter, L. G., D’Orazio, J. A., and Pearson, K. J. (2014). Resveratrol and cancer: focus on in vivo evidence. Endocr. Relat. Cancer 21, R209–R225. doi: 10.1530/ERC-13-0171
Casanova, F., Quarti, J., da Costa, D. C., Ramos, C. A., da Silva, J. L., and Fialho, E. (2012). Resveratrol chemosensitizes breast cancer cells to melphalan by cell cycle arrest. J. Cell. Biochem. 113, 2586–2596. doi: 10.1002/jcb.24134
Cavalieri, E., and Rogan, E. (2014). The molecular etiology and prevention of estrogen-initiated cancers: Ockham’s Razor: pluralitas non est ponenda sine necessitate. Plurality should not be posited without necessity. Mol. Aspects Med. 36, 1–55. doi: 10.1016/j.mam.2013.08.002
Cavalieri, E. L., and Rogan, E. G. (2010). Depurinating estrogen–DNA adducts in the etiology and prevention of breast and other human cancers. Future Oncol. 6, 75–91. doi: 10.2217/fon.09.137
Chan, A. T., Ogino, S., and Fuchs, C. S. (2007). Aspirin and the risk of colorectal cancer in relation to the expression of COX-2. N. Engl. J. Med. 356, 2131–2142. doi: 10.1056/NEJMoa067208
Chatterjee, K., Zhang, J., Honbo, N., and Karliner, J. S. (2010). Doxorubicin cardiomyopathy. Cardiology 115, 155–162. doi: 10.1159/000265166
Chedea, V. S., Vicaş, S. I., Sticozzi, C., Pessina, F., Frosini, M., Maioli, E., et al. (2017). Resveratrol: from diet to topical usage. Food Funct. 8, 3879–3892. doi: 10.1039/c7fo01086a
Chen, W., Zheng, R., Baade, P. D., Zhang, S., Zeng, H., Bray, F., et al. (2016). Cancer statistics in China, 2015. CA Cancer J. Clin. 66, 115–132. doi: 10.3322/caac.21338
Cho, S., Namkoong, K., Shin, M., Park, J., Yang, E., Ihm, J., et al. (2017). Cardiovascular protective effects and clinical applications of resveratrol. J. Med. Food. 20, 323–334. doi: 10.1089/jmf.2016.3856
Cragg, G. M., and Pezzuto, J. M. (2016). Natural products as a vital source for the discovery of cancer chemotherapeutic and chemopreventive agents. Med. Princ. Pract. 25(Suppl. 2), 41–59. doi: 10.1159/000443404
de Brito Monteiro, A. L., Silva Monteiro, V. V., Navegantes-Lima, K. C., Ferreira Reis, J. F., de Souza Gomes, R., Silva Rodrigues, D. V., et al. (2017). Resveratrol role in autoimmune disease—a mini-review. Nutrients 9:1306. doi: 10.3390/nu9121306
Deavall, D. G., Martin, E. A., Horner, J. M., and Roberts, R. (2012). Drug-induced oxidative stress and toxicity. J. Toxicol. 2012:645460. doi: 10.1155/2012/645460
Dey, A., Guha, P., Chattopadhyay, S., and Bandyopadhyay, S. K. (2009). Biphasic activity of resveratrol on indomethacin-induced gastric ulcers. Biochem. Biophys. Res. Commun. 381, 90–95. doi: 10.1016/j.bbrc.2009.02.027
Di Meglio, P., Perera, G. K., and Nestle, F. O. (2011). The multitasking organ: recent insights into skin immune function. Immunity 35, 857–869. doi: 10.1016/j.immuni.2011.12.003
Draelos, Z. D. (2012). New treatments for restoring impaired epidermal barrier permeability: skin barrier repair creams. Clin. Dermatol. 30, 345–348. doi: 10.1016/j.clindermatol.2011.08.018
Dun, J., Chen, X., Gao, H., Zhang, Y., Zhang, H., and Zhang, Y. (2015). Resveratrol synergistically augments anti-tumor effect of 5-FU in vitro and in vivo by increasing S-phase arrest and tumor apoptosis. Exp. Biol. Med. 240, 1672–1681. doi: 10.1177/1535370215573396
Elshaer, M., Chen, Y., Wang, X. J., and Tang, X. (2018). Resveratrol: an overview of its anti-cancer mechanisms. Life Sci. 207, 340–349. doi: 10.1016/j.lfs.2018.06.028
Emadi, A., and Gore, S. D. (2010). Arsenic trioxide—an old drug rediscovered. Blood Rev. 24, 191–199. doi: 10.1016/j.blre.2010.04.001
Fan, G., Tang, J. J., Bhadauria, M., Nirala, S. K., Dai, F., Zhou, B., et al. (2009). Resveratrol ameliorates carbon tetrachloride-induced acute liver injury in mice. Environ. Toxicol. Pharmacol. 28, 350–356. doi: 10.1016/j.etap.2009.05.013
Frémont, L. (2000). Biological effects of resveratrol. Life Sci. 66, 663–673. doi: 10.1016/S0024-3205(99)00410-5
Gao, L., Lee, S. S., Chen, J., Sun, H., Zhao, Y., Chai, Z., et al. (2016). High-throughput screening of substrate specificity for protein tyrosine phosphatases (ptps) on phosphopeptide microarrays. Methods Mol. Biol. 1368, 181–196. doi: 10.1007/978-1-4939-3136-1_13
Gray, B. P., and Brown, K. C. (2013). Combinatorial peptide libraries: mining for cell-binding peptides. Chem. Rev. 114, 1020–1081. doi: 10.1021/cr400166n
Hanna, A. D., Lam, A., Tham, S., Dulhunty, A. F., and Beard, N. A. (2014). Adverse effects of doxorubicin and its metabolic product on cardiac RyR2 and SERCA2A. Mol. Pharmacol. 86, 438–449. doi: 10.1124/mol.114.093849
He, X., Wang, Y., Zhu, J., Orloff, M., and Eng, C. (2011). Resveratrol enhances the anti-tumor activity of the mTOR inhibitor rapamycin in multiple breast cancer cell lines mainly by suppressing rapamycin-induced AKT signaling. Cancer Lett. 301, 168–176. doi: 10.1016/j.canlet.2010.11.012
Henderson, B. E., and Feigelson, H. S. (2000). Hormonal carcinogenesis. Carcinogenesis 21, 427–433. doi: 10.1093/carcin/21.3.427
Huang, W., Ding, L., Huang, Q., Hu, H., Liu, S., Yang, X., et al. (2010). Carbonyl reductase 1 as a novel target of (-)-epigallocatechin gallate against hepatocellular carcinoma. Hepatology 52, 703–714. doi: 10.1002/hep.23723
Ito, Y., Mitani, T., Harada, N., Isayama, A., Tanimori, S., TAkENAkA, S., et al. (2013). Identification of carbonyl reductase 1 as a resveratrol-binding protein by affinity chromatography using 4’-amino-3, 5-dihydroxy-trans-stilbene. J. Nutr. Sci. Vitaminol. 59, 358–364. doi: 10.3177/jnsv.59.358
Jang, M., Cai, L., Udeani, G. O., Slowing, K. V., Thomas, C. F., Beecher, C. W., et al. (1997). Cancer chemopreventive activity of resveratrol, a natural product derived from grapes. Science 275, 218–220. doi: 10.1126/science.275.5297.218
Jazirehi, A. R., and Bonavida, B. (2004). Resveratrol modifies the expression of apoptotic regulatory proteins and sensitizes non-Hodgkin’s lymphoma and multiple myeloma cell lines to paclitaxel-induced apoptosis. Mol. Cancer Ther. 3, 71–84.
Jee, J., Lim, J., Ong, Y. S., Oon, J., Gao, L., Choi, H. S., et al. (2016). An efficient strategy to enhance binding affinity and specificity of a known isozyme inhibitor. Org. Biomol. Chem. 14, 6833–6839. doi: 10.1039/c6ob01104g
Ji, Y., Cai, L., Zheng, T., Ye, H., Rong, X., Rao, J., et al. (2015). The mechanism of UVB irradiation induced-apoptosis in cataract. Mol. Cell. Biochem. 401, 87–95. doi: 10.1007/s11010-014-2294-x
Ko, J., Sethi, G., Um, J., Shanmugam, M. K., Arfuso, F., Kumar, A. P., et al. (2017). The role of resveratrol in cancer therapy. Int. J. Mol. Sci. 18, 2589–2624. doi: 10.3390/ijms18122589
Ko, J., Tsai, C., Liu, T., Lin, M., Lin, H., and Ou, C. (2016). Differential effects of grape juice on gastric emptying and renal function from cisplatin-induced acute adverse toxicity. Hum. Exp. Toxicol. 35, 808–817. doi: 10.1177/0960327115607079
Komina, O., and Wsierska-Gądek, J. (2008). Action of resveratrol alone or in combination with roscovitine, a CDK inhibitor, on cell cycle progression in human HL-60 leukemia cells. Biochem. Pharmacol. 76, 1554–1562. doi: 10.1016/j.bcp.2008.08.002
Kotecha, R., Takami, A., and Espinoza, J. L. (2016). Dietary phytochemicals and cancer chemoprevention: a review of the clinical evidence. Oncotarget 7, 52517–52529. doi: 10.18632/oncotarget.9593
Kundu, J. K., and Surh, Y. (2008). Cancer chemopreventive and therapeutic potential of resveratrol: mechanistic perspectives. Cancer Lett. 269, 243–261. doi: 10.1016/j.canlet.2008.03.057
Lee, Y., Lee, Y., Im, J., Won, S. Y., Kim, Y., Cho, M., et al. (2013). Synergistic anti-cancer effects of resveratrol and chemotherapeutic agent clofarabine against human malignant mesothelioma MSTO-211H cells. Food. Chem. Toxicol. 52, 61–68. doi: 10.1016/j.fct.2012.10.060
Liu, J., Liu, Y., Goyer, R. A., Achanzar, W., and Waalkes, M. P. (2000). Metallothionein-I/II null mice are more sensitive than wild-type mice to the hepatotoxic and nephrotoxic effects of chronic oral or injected inorganic arsenicals. Toxicol. Sci. 55, 460–467. doi: 10.1093/toxsci/55.2.460
Liu, X., Bao, H., Zeng, X., and Wei, J. (2016). Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease. Mol. Med. Rep. 13, 4266–4272. doi: 10.3892/mmr.2016.5057
Lucas, R. M., McMichael, A. J., Armstrong, B. K., and Smith, W. T. (2008). Estimating the global disease burden due to ultraviolet radiation exposure. Int. J. Epidemiol. 37, 654–667. doi: 10.1093/ije/dyn017
Monsuez, J., Charniot, J., Vignat, N., and Artigou, J. (2010). Cardiac side-effects of cancer chemotherapy. Int. J. Cardiol. 144, 3–15. doi: 10.1016/j.ijcard.2010.03.003
Nawaz, W., Zhou, Z., Deng, S., Ma, X., Ma, X., Li, C., et al. (2017). Therapeutic versatility of resveratrol derivatives. Nutrients 9, 1188–1213. doi: 10.3390/nu9111188
Ndiaye, M., Philippe, C., Mukhtar, H., and Ahmad, N. (2011). The grape antioxidant resveratrol for skin disorders: promise, prospects, and challenges. Arch. Biochem. Biophys. 508, 164–170. doi: 10.1016/j.abb.2010.12.030
Ong, Y. S., Gao, L., Kalesh, K. A., Yu, Z., Wang, J., Liu, C., et al. (2017). Recent advances in synthesis and identification of cyclic peptides for bioapplications. Curr. Top. Med. Chem. 17, 2302–2318. doi: 10.2174/1568026617666170224121658
Patrono, C., García Rodríguez, L. A., Landolfi, R., and Baigent, C. (2005). Low-dose aspirin for the prevention of atherothrombosis. N. Engl. J. Med. 353, 2373–2383. doi: 10.1056/NEJMra052717
Piska, K., Koczurkiewicz, P., Bucki, A., Wójcik-Pszczoła, K., Kołaczkowski, M., and Pękala, E. (2017). Metabolic carbonyl reduction of anthracyclines—role in cardiotoxicity and cancer resistance. Reducing enzymes as putative targets for novel cardioprotective and chemosensitizing agents. Invest. New Drugs 35, 375–385. doi: 10.1007/s10637-017-0443-2
Pruthi, S., Yang, L., Sandhu, N. P., Ingle, J. N., Beseler, C. L., Suman, V. J., et al. (2012). Evaluation of serum estrogen-DNA adducts as potential biomarkers for breast cancer risk. J. Steroid Biochem. Mol. Biol. 132, 73–79. doi: 10.1016/j.jsbmb.2012.02.002
Reagan-Shaw, S., Afaq, F., Aziz, M. H., and Ahmad, N. (2004). Modulations of critical cell cycle regulatory events during chemoprevention of ultraviolet B-mediated responses by resveratrol in SKH-1 hairless mouse skin. Oncogene 23, 5151–5160. doi: 10.1038/sj.onc.1207666
Revel, A., Raanani, H., Younglai, E., Xu, J., Rogers, I., Han, R., et al. (2003). Resveratrol, a natural aryl hydrocarbon receptor antagonist, protects lung from DNA damage and apoptosis caused by benzo [a] pyrene. J. Appl. Toxicol. 23, 255–261. doi: 10.1002/jat.916
Riba, A., Deres, L., Sumegi, B., Toth, K., Szabados, E., and Halmosi, R. (2017). Cardioprotective effect of resveratrol in a postinfarction heart failure model. Oxid. Med. Cell. Longev. 2017:6819281. doi: 10.1155/2017/6819281
Sarkar, F. H., Li, Y., Wang, Z., and Kong, D. (2009). Cellular signaling perturbation by natural products. Cell. Signal. 21, 1541–1547. doi: 10.1016/j.cellsig.2009.03.009
Sarubbo, F., Moranta, D., Asensio, V. J., Miralles, A., and Esteban, S. (2017). Effects of resveratrol and other polyphenols on the most common brain age-related diseases. Curr. Med. Chem. 24, 4245–4266. doi: 10.2174/0929867324666170724102743
Şener, G., Toklu, H. Z., Şehirli, A. Ö, Velioğlu-Öğünç, A., Çetinel, S., and Gedik, N. (2006). Protective effects of resveratrol against acetaminophen-induced toxicity in mice. Hepatol. Res. 35, 62–68. doi: 10.1016/j.hepres.2006.02.005
Shen, B. (2015). A new golden age of natural products drug discovery. Cell 163, 1297–1300. doi: 10.1016/j.cell.2015.11.031
Sheu, M., Jhan, H., Hsieh, C., Wang, C., and Ho, H. (2015). Efficacy of antioxidants as a complementary and alternative medicine (CAM) in combination with the chemotherapeutic agent doxorubicin. Integr. Cancer Ther. 14, 184–195. doi: 10.1177/1534735414564425
Shukla, S., Ohnuma, S., and Ambudkar, S. V. (2011). Improving cancer chemotherapy with modulators of ABC drug transporters. Curr. Drug Targets 12, 621–630. doi: 10.2174/138945011795378540
Siegel, R. L., Miller, K. D., and Jemal, A. (2016). Cancer statistics, 2016. CA Cancer J. Clin. 66, 7–30. doi: 10.3322/caac.21332
Siegel, R. L., Miller, K. D., and Jemal, A. (2017). Cancer statistics, 2017. CA Cancer J. Clin. 67, 7–30. doi: 10.3322/caac.21387
Šimůnek, T., Štěrba, M., Popelová, O., Adamcová, M., Hrdina, R., and Geršl, V. (2009). Anthracycline-induced cardiotoxicity: overview of studies examining the roles of oxidative stress and free cellular iron. Pharm. Res. 61, 154–171. doi: 10.1016/S1734-1140(09)70018-0
Tessitore, L., Davit, A., Sarotto, I., and Caderni, G. (2000). Resveratrol depresses the growth of colorectal aberrant crypt foci by affecting bax and p21 CIP expression. Carcinogenesis 21, 1619–1622. doi: 10.1093/carcin/21.8.1619
Thorat, M. A., and Cuzick, J. (2013). Role of aspirin in cancer prevention. Curr. Oncol. Rep. 15, 533–540. doi: 10.1007/s11912-013-0351-3
Thun, M. J., Jacobs, E. J., and Patrono, C. (2012). The role of aspirin in cancer prevention. Nat. Rev. Clin. Oncol. 9, 259–267. doi: 10.1038/nrclinonc.2011.199
Upadhyay, G., Singh, A. K., Kumar, A., Prakash, O., and Singh, M. P. (2008). Resveratrol modulates pyrogallol-induced changes in hepatic toxicity markers, xenobiotic metabolizing enzymes and oxidative stress. Eur. J. Pharmacol. 596, 146–152. doi: 10.1016/j.ejphar.2008.08.019
Vos, T., Allen, C., Arora, M., Barber, R. M., Bhutta, Z. A., Brown, A., et al. (2016). Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet 388, 1545–1602. doi: 10.1016/S0140-6736(16)31678-6
Vuky, J., Yu, R., Schwartz, L., and Motzer, R. J. (2002). Phase II trial of arsenic trioxide in patients with metastatic renal cell carcinoma. Invest. New Drugs 20, 327–330. doi: 10.1023/A:1016270206374
Wang, J., Gao, L., Lee, Y. M., Kalesh, K. A., Ong, Y. S., Lim, J., et al. (2016). Target identification of natural and traditional medicines with quantitative chemical proteomics approaches. Pharmacol. Ther. 162, 10–22. doi: 10.1016/j.pharmthera.2016.01.010
Wang, L., Kou, M., Weng, C., Hu, L., Wang, Y., and Wu, M. (2012). Arsenic modulates heme oxygenase-1, interleukin-6, and vascular endothelial growth factor expression in endothelial cells: roles of ROS, NF-κB, and MAPK pathways. Arch. Toxicol. 86, 879–896. doi: 10.1007/s00204-012-0845-z
Waxman, S., and Anderson, K. C. (2001). History of the development of arsenic derivatives in cancer therapy. Oncologist 6(Suppl. 2), 3–10. doi: 10.1634/theoncologist.6-suppl_2-3
Westervelt, P., Brown, R. A., Adkins, D. R., Khoury, H., Curtin, P., Hurd, D., et al. (2001). Sudden death among patients with acute promyelocytic leukemia treated with arsenic trioxide. Blood 98, 266–271. doi: 10.1182/blood.V98.2.266
Wu, S. L., Sun, Z. J., Yu, L., Meng, K. W., Qin, X. L., and Pan, C. E. (2004). Effect of resveratrol and in combination with 5-FU on murine liver cancer. World J. Gastroenterol. 10, 3048–3052. doi: 10.3748/wjg.v10.i20.3048
Xiao, Q., Wu, J., Pang, X., Jiang, Y., Wang, P., Leung, A. W., et al. (2018). Discovery and development of natural products and their derivatives as photosensitizers for photodynamic therapy. Curr. Med. Chem. 25, 839–860. doi: 10.2174/0929867324666170823143137
Xiao, Z., Chen, C., Meng, T., Zhang, W., and Zhou, Q. (2016). Resveratrol attenuates renal injury and fibrosis by inhibiting transforming growth factor-β pathway on matrix metalloproteinase 7. Exp. Biol. Med. 241, 140–146. doi: 10.1177/1535370215598401
Yu, M., Xue, J., Li, Y., Zhang, W., Ma, D., Liu, L., et al. (2013). Resveratrol protects against arsenic trioxide-induced nephrotoxicity by facilitating arsenic metabolism and decreasing oxidative stress. Arch. Toxicol. 87, 1025–1035. doi: 10.1007/s00204-013-1026-4
Zahid, M., Gaikwad, N. W., Rogan, E. G., and Cavalieri, E. L. (2007). Inhibition of depurinating estrogen- DNA adduct formation by natural compounds. Chem. Res. Toxicol. 20, 1947–1953. doi: 10.1021/tx700269s
Zahid, M., Saeed, M., Beseler, C., Rogan, E. G., and Cavalieri, E. L. (2011). Resveratrol and N-acetylcysteine block the cancer-initiating step in MCF-10F cells. Free Radical. Biol. Med. 50, 78–85. doi: 10.1016/j.freeradbiomed.2010.10.662
Zhang, P., Wang, S., Hu, L., Qiu, F., Yang, H., Xiao, Y., et al. (2000). Seven years’ summary report on the treatment of acute promyelocytic leukemia with arsenic trioxide–an analysis of 242 cases. Chin. J. Hematol. 21, 67–70.
Zhang, W., Xue, J., Ge, M., Yu, M., Liu, L., and Zhang, Z. (2013). Resveratrol attenuates hepatotoxicity of rats exposed to arsenic trioxide. Food Chem. Toxicol. 51, 87–92. doi: 10.1016/j.fct.2012.09.023
Zhao, X., Li, G., Liu, Y., Chai, L., Chen, J., Zhang, Y., et al. (2008). Resveratrol protects against arsenic trioxide-induced cardiotoxicity in vitro and in vivo. Br. J. Pharmacol. 154, 105–113. doi: 10.1038/bjp.2008.81
Zhou, F., Hao, G., Zhang, J., Zheng, Y., Wu, X., Hao, K., et al. (2015). Protective effect of 23-hydroxybetulinic acid on doxorubicin-induced cardiotoxicity: a correlation with the inhibition of carbonyl reductase-mediated metabolism. Br. J. Pharmacol. 172, 5690–5703. doi: 10.1111/bph.12995
Keywords: natural products, resveratrol, cancer, chemotherapy, side effects
Citation: Xiao Q, Zhu W, Feng W, Lee SS, Leung AW, Shen J, Gao L and Xu C (2019) A Review of Resveratrol as a Potent Chemoprotective and Synergistic Agent in Cancer Chemotherapy. Front. Pharmacol. 9:1534. doi: 10.3389/fphar.2018.01534
Received: 01 July 2018; Accepted: 17 December 2018;
Published: 09 January 2019.
Edited by:
Hongjie Zhang, Hong Kong Baptist University, Hong KongReviewed by:
Jelena Cvejic, University of Novi Sad, SerbiaTie-Jun Li, Second Military Medical University, China
Francesco Michelangeli, University of Chester, United Kingdom
Copyright © 2019 Xiao, Zhu, Feng, Lee, Leung, Shen, Gao and Xu. 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: Chuanshan Xu, xcshan@163.com Jun Shen, shenjun@mail.sysu.edu.cn Liqian Gao, gaolq@mail.sysu.edu.cn; glqustc@gmail.com
†These authors have contributed equally to this work