- 1State Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, China
- 2Guangdong-Hong Kong-Macau Joint Lab on Chinese Medicine and Immune Disease Research, Macao, Macao SAR, China
- 3Dr. Neher’s Biophysics Laboratory for Innovative Drug Discovery/State Key Laboratory of Quality Research in Chinese Medicine/Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macao, Macao SAR, China
- 4Department of Oncology, Luzhou People’s Hospital, Luzhou, Sichuan, China
- 5Cancer Center, Faculty of Health Science, University of Macau, Macao, Macao SAR, China
- 6MOE Frontiers Science Center for Precision Oncology, University of Macau, Macao, Macao SAR, China
- 7Breast Surgery, Zhuhai Hospital of Traditional Chinese and Western Medicine, Zhuhai, China
Biologically active sphingolipids are closely related to the growth, differentiation, aging, and apoptosis of cancer cells. Some sphingolipids, such as ceramides, are favorable metabolites in the sphingolipid metabolic pathway, usually mediating antiproliferative responses, through inhibiting cancer cell growth and migration, as well as inducing autophagy and apoptosis. However, other sphingolipids, such as S1P, play the opposite role, which induces cancer cell transformation, migration and growth and promotes drug resistance. There are also other sphingolipids, as well as enzymes, played potentially critical roles in cancer physiology and therapeutics. This review aimed to explore the important roles of sphingolipid metabolism in cancer. In this article, we summarized the role and value of sphingolipid metabolism in cancer, including the distribution of sphingolipids, the functions, and their relevance to cancer diagnosis and prognosis. We also summarized the known and potential antitumor targets present in sphingolipid metabolism, analyzed the correlation between sphingolipid metabolism and tumor immunity, and summarize the antitumor effects of natural compounds based on sphingolipids. Through the analysis and summary of sphingolipid antitumor therapeutic targets and immune correlation, we aim to provide ideas for the development of new antitumor drugs, exploration of new therapeutic means for tumors, and study of immunotherapy resistance mechanisms.
Introduction
Over the last 2–3 decades, we have gained a great understanding of the structural biodiversity, cell biology, metabolisms, and pathology of sphingolipids. Various molecules from this lipid family participate in a variety of cellular functions in health and disease (1). As shown in Figure 1, ceramides constitute the hub of sphingolipid metabolism and participate in the synthesis and catabolic metabolism of sphingolipids. Ceramides can be generated through several different mechanisms. Endogenous ceramides can be synthesized via de novo pathway following the action of a range of enzymes, such as serine palmitoyltransferase (SPT), ceramide synthase (CerS), and dihydroceramide desaturase (DES). Ceramides may also be produced through the decomposition of membrane sphingomyelins (SMs) or the degradation of complex sphingolipids under the action of sphingomyelinases (SMase) and glucosylceramidases, respectively. In addition, sphingosine, a product of sphingolipid catabolism, can be reacylated by CerS, resulting in the production of ceramides. Once produced, ceramides can briefly accumulate or be converted into different, sphingolipids, such as ceramide 1-phosphate (C1P), sphingosine 1-phosphate (S1P), and glucosylceramide (GlcCer). Ceramide can also be reversed into SMs, that is, phosphorylcholine and ceramide generate SMs under the action of sphingomyelin synthetase (SMS). In addition, ceramides can be glycosylated by different enzymes of the Golgi Apparatus into glycosphingolipids (GSLs). Moreover, sphingolipids are also glycosylated in the lysosomes (2). The phosphorylation of ceramide also occurs in Golgi Apparatus by CerK (3) (Figure 1).
The mortality rate caused by malignant tumors has nearly doubled in the last two decades (4), and cancer remains the highest cause of mortality worldwide. Sphingolipids and tumors are closely related. The correlation between them has received increasing attention from researchers. Sphingolipids, among all the reasons for the pathogenesis of cancer researched thus far, play a critical role in the initial and developmental stages of cancer. Sphingolipids serve as bioeffectors that coordinate all aspects of cancer biology, including apoptosis, cell proliferation, and cell migration. Ceramide and S1P are important sphingolipids but have opposite effects. Ceramide promotes cancer cells apoptosis, blocks cell growth; S1P promotes cancer cells survival, enhancing cell proliferation, angiogenesis. The dynamic balance of these two opposing sphingolipids is called the “Sphingolipid rheostat” (5). The sphingolipid-regulated processes are critical for the development, progression, metastasis, and drug resistance of different types of cancers (1).
The value of sphingolipid metabolism in cancer
The expression level of sphingolipids related to cancer diagnosis and prognosis
Sphingolipids are also expressed differently in various tumor subtypes. Recent studies have shown that some classes of ceramides may be elevated in certain human malignancies. For example, C16:0 and C24:1 ceramides are up-regulated in node-positive pancreatic tissues (6). Similar observations on up-regulated sphingolipids have been found for B16 melanoma, murine sarcoma 180, and Lewis lung carcinoma (7); human head and neck squamous cell carcinoma (HNSCC) (8); rat nephroma-RA (9); and breast cancer (10). By contrast, colon cancer (11), ovarian carcinoma (12), and human astrocytoma (13) have lower ceramide levels than their corresponding healthy organizations. in certain human malignancies, since in some works depending on the species, their levels are decreased. Another published report found that C18-Cer is selectively down-regulated in HNSCC relative to in nonsquamous tumor tissues (14).
Then, in the downstream of sphingolipid pathways, the activity of SPHK1/S1P plays an important role in many cancers, and SPHK1 has been proven to be highly expressed in a variety of cancers (15–17). An investigation has been applied to test the tissue samples from prostate cancer patients and healthy individuals. The results proved that SPHK1 expression is 2-fold higher in tissues from patients than in healthy individuals (18). This phenomenon had also been observed in breast cancer. For example, a previous work performed microarray analysis on various subtypes in 1269 breast cancer samples and found increased SPHK1 expression in the tissues of patients with cancer (19). Another study showed that, in breast cancer, SPHK1 and ceramide galactosyltransferase (UGT8) are highly expressed in ER-negative tumors, and dihydroceramide synthases (LASS4 and LASS 6), acid ceramidase (ACDase), and glucosylceramide synthase (GCS) are highly expressed in ER-positive samples (19). Moreover, numerous other cancers have high SPHK1 expression (20–23). These cancers include oral squamous cell carcinoma (24), gastric cancer (15), hepatocellular carcinoma (HCC) (16, 17), glioblastoma multiforme (20), prostate cancer (21), esophageal cancer (22), and HNSCC (23) (Table 1). All the above pieces of information show that the cell-transformation-related alterations in sphingolipid metabolism are dependent on cancer types. We have summarized the abnormal sphingolipid metabolism of different cancers in Table 1. Changes in sphingolipid metabolism contribute to the progress of cancers and provide useful targets for the development of new targeted therapies. Moreover, some sphingolipids could be used as biomarkers in cancer diagnosis. The latest data have shown that in patients with breast cancer, the increase in C16-Cer is associated with metastatic lymph node (LN) status (10), suggesting that C16-Cer has metastatic potential in the clinic. Interestingly, an investigation on colorectal cancer (CRC) tissue has suggested that CRC shows increased amounts of S1P, Sph, and C14-Cer and markedly reduced amounts of C18-Cer and C20-Cer. The circulating contents of C16:0-Cer, C18:1-Cer, C20-Cer, and C24:1-Cer in more advanced CRC were higher than those in early lesions (32). These results suggest that early lesions can be distinguished from advanced CRC through the combined determination of the plasma concentrations of several ceramides. In addition to being the diagnostic biomarkers, sphingolipids could also be used as biomarkers in cancer prognosis. Clinical studies have reported that the expression levels of SPHK and S1P are associated with patient survival and cancer metastasis (22, 23). An online database of gene expression and clinical data from 1928 patients with NSCLC has showed that although the high expression of SPHK1 mRNA is significantly correlated with worsened overall survival (OS), the high expression of SPHK2 mRNA is correlated with improved OS (23). Interestingly, in esophageal cancer, the high expression of SPHK1 is associated with poor 5-year OS and increased SPHK1 levels are significantly correlated with LN metastasis; therefore, SPHK1 is a potential biomarker for outcome prediction in clinical practice (22). A meta-analysis has shown that increased SPHK1 expression is associated with poor prognosis in human cancers and could be a promising prognostic marker and therapeutic target in patients with malignancies (33). Despite SPHK1 and SPHK2 are highly homologous, different subsets of SPHK execute different physiological roles in cancers. However, both subtypes have important roles in inducing cancer cell survival (34, 35).
The function of sphingolipids in cancer
An increasing number of studies have explored the correlations between sphingolipids and tumors. The dynamic balance among sphingolipids maintains normal biological functions. In cancer, however, this balance can be disrupted. A growing body of evidence shows that in cancer, the levels of bioactive sphingolipids are altered. Thus, bioactive sphingolipids harbor the potential to act as important cancer biomarkers for the determination of disease progression (36). Given the different expression levels of metabolites in different cancers, the same sphingolipids could execute opposite roles in different cancers.
Ceramides are one of the most studied sphingolipids in cancers due to their role in cell differentiation and death. Diverse ceramides produce different lengths of ceramide chains that have unique and important biological functions in vivo. Ceramides can induce apoptosis through the mitochondrial pathway by changing the mitochondrial ultrastructure and reducing mitochondrial function and membrane potential, thus ultimately inducing apoptosis (37). For example, C18-Cer could modulate telomerase activity and mitochondrial dysfunction-induced apoptotic cell death in HNSCC (14), and C16-Cer could induce ER stress-mediated apoptosis in lung cancer (38). Ceramides can also cause cell death via autophagy. In liver and nasopharyngeal cancers, ceramides could induce autophagy through the regulation of Beclin-1 (39). Dihydroceramide could also activate the unfolded protein response that leads to cytotoxic autophagy in cancer cells (40). In colon cancer, ceramide inhibits cell proliferation and migration by down-regulating IL-10, STAT3, and NF-kB expression (41). Another published report has shown that in breast cancer, the overexpression of C16-Cer reduces the phosphorylation of Akt/mTOR and ERK (42). Ceramides have numerous mechanisms for cell death induction. Instead of inhibiting cell growth as mentioned above (42), C16-Cer protects against ER stress-induced apoptosis and enhances tumor development and growth in HNSCC (43). Similarly, ceramide has an opposite effect in colon cancer that is distinct from their effect in gallbladder cancer (44). C24-Cer induces cell proliferation and migration by binding to PIP4K2C to facilitate mTOR complex formation and activation (45) (Table 2).
In contrast to ceramides, S1P can modulate multifunctional biological activities in cancer, such as proliferation, migration, inflammation, and angiogenesis. As proposed by Hanahan and Weinberg, S1P is involved in all features of cancer, including sustained proliferative signaling, the evasion of growth inhibitors, resistance to apoptosis, the achievement of uncontrolled replication, angiogenesis, the activation of invasion and metastasis, the reprogramming of energy metabolism, and the evasion of the immune response (78). The generation of S1P from sphingosine is catalyzed by two SPHK isoforms, namely, SPHK1 and SPHK2. S1P receptors are called S1PR. S1P binds to five high-affinity G-coupled receptors with different tissue distribution patterns: S1PR 1–5. The specific role of S1P is dominated by the expressed S1PR subtype (44).
Similar to vascular endothelial growth factor, S1P has been reported to increase vascular permeability. The mechanism of activation involves the activation of the S1PR2 subtype and requires Rho/ROCK/PTEN signal transduction (79). In lymphatic cancer, S1P could prevent apoptosis by inhibiting the translocation of cytochrome c and Smac/DIABLO from the mitochondria to the cytoplasm (53). S1P has also been shown to influence the metastasis and migration of cancer cells. For example, S1P could induce HCC metastasis via establishing the MMP-7/syndecan-1/TGF-β1 autocrine loop (55). Moreover, it could stimulate the chemotaxis and invasion of ovarian cancer cells in a receptor-dependent manner that involves the activation of ERK, AKT, and p38 (43).
The function of sphingolipid enzymes in cancer
The abundance of sphingolipids is controlled by metabolic enzymes, which have a crucial role in regulating cancer cell death or survival as summarized in Table 2. Thus, we next focus on the enzymes participating in cancer physiology. Some enzymes have been proven to be capable of enhancing ceramide synthesis and break down S1P to promote cancer cell death. These enzymes include SMase, SPT, CerS, DES, and S1P lyase (SPL), which need therapeutic activators (1). On the other hand, some enzymes that could eliminate and metabolize ceramides, such as CerK, CDase, SPHK, and SMS, which need therapeutic inhibitors.
SMase is a sphingolipid enzyme that has been widely reported. It can be divided into three types in accordance with its optimal pH-dependent activity: acid SMase (ASMase), neutral SMase (NSMase), and alkaline SMase (alk-SMase) (45). Many pieces of evidence had suggested that the activation of ASMase is a necessary step for the initiation of apoptosis in stress-induced ceramide elevation (62). NSMase has also been reported to cause apoptosis in cancer (63, 64). In addition, the lack of alk-SMase has been shown to be capable of significantly increasing colon tumorigenesis (80).
Another one, SPHK1, can promote proliferation and migration by promoting JAK/STAT activation and up-regulating S1PR1 expression (81). SPHK1 promotes triple negative breast cancer (TNBC) translocation through the S1P/S1PR3/Notch signaling pathway (29). Convincing evidence indicates that the activation of SPHK1 contributes to cancer progression and tumor growth and impairs cancer cell apoptosis via suppressing STAT1 expression (72), as well as activating the ERK1/2 and PI3K/AKT pathways (29) Many studies have demonstrated that the activation of SPHK1 can induce cancer cell migration, and that the SPHK1/S1P axis enhances the metastatic potential of cancer cells. Mechanism studies have reported that SPHK1 increases the expression of Slug, vimentin, N-cadherin, and FAK in colon cancer (82) Notably, the active interaction of SPHK1 or S1P with ERK pathway promotes autophagy in colon cancer (68).
CerK is a calcium ion-dependent enzyme that catalyzes the production of C1P in cells. Intracellular C1P can perform a variety of biological functions, including the stimulation of tumor cell growth, the stimulation of VEGF release, the inhibition of tumor cell apoptosis, the promotion of tumor inflammation, the regulation of angiogenesis, and the stimulation of tumor cell migration (83–85). C1P regulates the invasion and migration of different types of cancer cells, including breast, lung, prostate, pancreas or leukemia cells (83). CerK phosphorylates cell-killing ceramides into C1P. The metabolic conversion of ceramide into SM is catalyzed by SMS. CerK and SMS can induce migration and invasion (61, 65). Some sphingolipid enzymes also have dual roles in different cancers as illustrated by CerK. Although CerK can regulate Rac1 activity and inhibit lamellipodium formation in A549 cells (60), it can promote migration in breast cancer (61).
The role of sphingolipids as therapeutic targets in cancer
Sphingolipid-based anti-tumor treatment strategy
Sphingolipids are currently recognized as multifaceted mediators in the biological and therapeutic fields of cancer. Therefore, they may become new targets for therapeutic application. Sphingolipid metabolism is becoming increasingly well studied in this field of cancer treatment. Several types of cytotoxic chemotherapeutic agents that cause ceramide accumulation, including doxorubicin, irinotecan, vincristine, and paclitaxel, have been clinically applied or undergoing clinical trials (43).
Although sphingolipids have been demonstrated to have an effective antitumor action, their poor solubility, uptake, bioavailability, and metabolic transformation have hindered the efforts to utilize their antitumor effect. Therefore, determining a way to improve efficacy is necessary for the development of ceramide-based therapy (Figure 2). For example, a previous work showed that in cultured TNBC cells, nanoliposomal tamoxifen enhances nanoliposomal C6-ceramide cytotoxicity. This reaction is accompanied by the induction of cell cycle arrest in G1 and G2 by caspase-induced DNA fragmentation. The permeability of the mitochondria and lysosomal membrane was enhanced at 18 and 2 h, respectively (86). The combination of C6-ceramide nanoliposomes with PPMP has been shown to lead to an increase in endogenous long-chain ceramide species, resulting in the apoptosis of leukemic natural killer (NK) cells via the mitochondrial endogenous cell death pathway (87). Moreover, in mice with hepatic tumors, the injection of nanoliposome-loaded LipC6 reduces the amount of tumor-associated macrophages and the ability of TAMs to inhibit the antitumor immune response. LipC6 also enhances the antitumor activity of tumor antigen-specific CD8+ T cells (88). A novel method for loading the short-chain C6 ceramide onto polyethylene glycol and polyethyleneimine co-conjugated ultra-small nano-GO can also result in high cancer-cell-killing potential in HCC (89).
Anti-tumor treatment strategy based on sphingolipid enzymes
In addition to sphingolipids, sphingolipid enzymes have also become important targets for anti-tumor selection. SMase could be activated after stimulation by radiation and chemotherapeutic drugs, such as leukemia and glioma. The activated SMase catalyzes the hydrolysis of SM to produce ceramide. The produced ceramide would continue to activate different protein kinases and protein phosphatases (JNK and PKC), thus initiating the cascade signaling pathway, transmitting extracellular signals to cells, and then causing apoptosis. Therefore, the inhibition of enzymes that break down ceramide can alleviate chemotherapy resistance via sphingolipid regulation. The inhibitors of sphingolipid-metabolizing enzymes can be used as chemical sensitizers (37). Interestingly, SPHK1 has also been reported to promote the oxaliplatin resistance of HCC cells via the modulation of the Akt/GSK3β signaling pathway (16). So, the SPHK1 inhibitor maybe reverses oxaliplatin resistance.
Given that the dysregulation of sphingolipid enzymes can lead to the occurrence of cancer, the discovery of the optimal characterized inhibitors and activators targeting sphingolipid enzymes is important. At present, many inhibitors for different types of sphingolipid enzymes, such as Acid ceramidase (ASAH1), ACDase, CerK, SPHK, and GCS, have been discovered (90). B13 is a ceramide analogue that has been shown to be an effective in vitro ACDase inhibitor (30). B13 can accumulate cellular ceramides in vivo. It has been modified with a series of lysosomotrophic molecules, such as LCL521 (30), to address its difficult accumulation in lysosomes. NVP-231 is a CerK inhibitor. NVP-231 decreases cell viability, DNA synthesis and colony formation in a concentration-dependent manner. It can increase DNA fragmentation and induce apoptosis (91). Dimethylsphingosine is a methylated form of sphingosine and is the first SPHK inhibitor (90). The SphK inhibitor is called SK I-II. SPHK I-II simultaneously inhibits SPHK1 and SPHK2, as well as other targets, and SPHK inhibition with SPHK I-II decreases MDR breast cancer proliferation and viability (92). FTY720, a sphingosine analogue that induces S1P receptor down-regulation, is another SPHK1 inhibitor (fingolimod). It inhibits SPHK1 and blocks the activation of multiple targets of this enzyme. It directly or indirectly inhibits multiple intracellular targets responsible for cell proliferation, migration, and angiogenesis (93). Moreover, preclinical data support its possible use as an antineoplastic drug (94). The GCS inhibitors D-threo-1-phenyl-2palmitoylamino-3-morpholino-l propanol (PPMP) and D-threo-1-phenyl-2-decanoylamino-3-morpholino-propanol (PDMP) are ceramide analogues. A study on leukemic cell lines has shown that by blocking GCS with PDMP and PPMP simultaneously, cells become desensitized to daunomycin because of the antiapoptotic action of galactoside ceramide accumulation (95). Thus, the effect of sphingolipid enzymes and their inhibitors on cancer cells is an interesting topic that needs further studies.
The role of sphingolipids in anti-cancer drug resistance
Drug resistance is a serious barrier to the successful therapy of patients with cancer. A large number of experiments have reported the mechanisms through which sphingolipids and their enzymes cause cancer drug resistance. Sphingolipid expression is also applied as a biomarker of drug resistance. The most widely known sphingolipid enzyme is GCS. This enzyme catalyzes the combination of glucose and ceramide to produce noncytotoxic GlcCer, which results in the decrement in cytotoxic Ceramide levels. The overexpression of GCS, which is particularly prominent in chemotherapy resistance, has been found in various cancers (96). In breast cancer, MDR1 overexpression is accompanied by other changes in genes, including GCS. MDR1 encodes P-glycoprotein, which could extrude anticancer drugs (97). Then, in breast cancer, high GCS expression is correlated with multidrug resistance (MDR), the poor prognosis of estrogen receptor (ER)+ tumors (30), and metastatic ER+ and human epidermal growth factor receptor 2 (HER2)+ tumors (Luminal B) (91). In ovcar-8 cancer cells, GCS transfection induces MDR1 overexpression and increases P-glycoprotein excretion in a dose-dependent manner. GSLs mediate MDR1 gene expression via cSrc and β-catenin signaling (97). In prostate cancer, SPHK1 inhibitors enhance the anticancer efficacy of enzalutamide (92). In addition, ceramide levels are lower in patients with chemoresistant leukemia than in patients with chemosensitive leukemia, whereas the activities of SMS and GCS in chemoresistant leukemia cells are higher than those in chemosensitive leukemia cells (98). Other studies have shown that sphingolipid enzymes, such as CDase and SPHK (99), are closely related to chemotherapy resistance.
The relationship between sphingolipid metabolism and tumor immunotherapy
Sphingolipids and tumor immunotherapy
A growing number of studies have demonstrated that metabolites in sphingolipid metabolism are closely associated with tumor immunity and that sphingolipids are involved in the interactions between cancer cells and the immune system. Sphingolipids are important components of the plasma membrane and can influence the function of receptors on the surfaces of immune cells. Metabolites are involved in the release of bioactive mediators, S1P, and ceramides, which influence the efflux and migration of lymphocytes into the tumor environment and regulate the critical pathways required for the activation of immune cells (100). The release of bioactive mediators, S1P, and ceramides can alter the function of immune cells, including Tregs lymphocytes, and macrophages, in the tumor microenvironment (TME), as well as alter the intracellular signaling pathways associated with immune cell activation or survival; such an alteration, in turn, may modulate the efficacy of antitumor immunotherapy (100). In a mouse model, ceramides inhibit the function of myeloid-derived suppressor cells (MDSCs) by activating lysosomal histone B and histone D; this effect leads to diminished autophagy and ER stress induction, thereby enhancing cytotoxic T lymphocyte function and inhibiting the growth of CMS4-met-derived soft tissue sarcoma tumors (77).
Other studies have reported that the metabolite C2-ceramide triggers apoptosis in melanoma cells by increasing PKCζ, as well as proinflammatory cytokines and signaling factors (101). C2-ceramide regulates immune cells in the TME and activates host protective immune responses through the up-regulation of PKCζ. In a PKCζ-dependent pathway, C2-ceramide repolarizes tumor-associated macrophages (TAMs) toward the M1 phenotype, thereby generating antitumor responses in vitro and in vivo (101). Ceramide-mediated alterations in host-protective angiogenic factors and alterations in T helper 1 cell (Th1) and T helper 2 cell (Th2) cytokine levels lead to improvements in the TME. C2-ceramide tilts the immune component within the TME toward a proinflammatory state and differentially regulates immune cell–cancer cell interactions to limit tumor growth. At the same time, C2-ceramide can increase the proportion of activated CD8+ T-cells in the TME and up-regulate perforin and granzyme B, which kill tumors in response (101).
Ceramides modified with nanomaterials can further modulate the efficacy of tumor immunotherapy. Nanoliposomal C6-ceramide (LipC6) not only induces apoptosis and prevents HCC-induced immune tolerance in HCC cells, it also significantly decelerates the growth of liver cancer cells, enhances tumor-infiltrating CD8+ T cells, and inhibits tumor-resident CD4+ CD25+ forkhead box protein P3 (FoxP3+) Treg cells in combination with anti-CTLA4 Ab (102). Molecular studies have shown that combination therapy inhibits the transcription factors Krüppel-like factor 2, FoxP3 and CTLA4 (102). The dysregulation of sphingolipid metabolism is also frequently associated with cancer stem cells (103, 104) and consequently generates a series of tumor immune-related effects; this situation suggests that ceramide is a key player in cancer immunotherapy (104). Elevated levels of ceramides induce cancer cell death (105), enhance the host protective immune response, and induce cancer regression (101, 106). Elevated levels of S1P induce an increase in the antiapoptotic proteins Bcl-2 and Bcl-XL in macrophages and the M2-type polarization of macrophages, which can also recruit immune cells to immune tissues for immune action (107, 108). S1P released from apoptotic or tumor cells, in combination with its specific receptor (S1PR1), induces the recruitment of circulating monocytes to the TME (109). α-Galactose ceramide (α-GalCer) has been noted for its role in activating invariant natural killer T (iNKT) lymphocytes and has been dicscovered to have a beneficial effect on the immune system. It has been noticed for its role in activating iNKT lymphocytes and has been found to exert oncogenic effects in a variety of tumors by inducing effective iNKT cells. The addition of PD-1 blockers to α-GalCer treatment prevents iNKT cell loss, resulting in the skewing of CD4+ cells toward Th1. This situation suggests that the combination of α-GalCer and immune checkpoint blockers may be a promising approach for improving the efficacy of tumor immunotherapy (110). In conclusion, sphingolipids are closely related to tumor immunity, and altered levels of sphingolipid metabolism are important factors influencing tumor immunotherapy (Figure 3).
Correlation between enzymes in the sphingolipid pathway and tumor immunotherapy
Now that we understand that sphingolipids are closely associated with tumor immunotherapy, we are eager to learn the exact mechanisms underlying the important roles of SMases in association with tumor immunotherapy. In different T cell subpopulations in mice and humans, sphingolipids are metabolized by varying degrees into ceramides that, in turn, participate in immune regulation and influence T cell activation, differentiation, and effector functions (111). ASMase (mouse: Asm; human: ASM) is a key mediator of sphingolipid catabolism. SMase deficiency impairs T-cell function, whereas increasing SMase activity increases T-cell function, thereby improving the efficacy of anticancer immunotherapy. These phenomena suggest that increasing ASM activity in T cells through drugs may enhance T cell-mediated immunity and may thus improve tumor killing (111).
Ceramide synthase 5 is one of six enzymes that catalyze the production of ceramides from sphingosine. Ceramides are an essential component of cell membranes and act as signaling molecules. CerS5 knockout mice have significantly reduced CD8+ T cells in the colonic epithelium. This decrement is accompanied by the reduced expression of IL-1β, IFNγ, and IL-4. The mice show increased susceptibility to colon cancer. In vitro studies have found that the knockdown of ceramide synthase 5 in T cells impairs T cell activation (112). Moreover, SPHK1 produced S1P is directly linked to the activity of the lipid transcription factor peroxisome proliferator-activated receptor γ, which subsequently regulates lipolysis in T cells. The inhibition of SPHK1 increases the antitumor activity of T cells against murine melanoma (113). Alkaline ceramidase 3 (Acer3) mediates the immune response by regulating C18:1-ceramide levels in the cells of the innate immune system, and Acer3 deficiency increases the levels of proinflammatory cytokines in colonic epithelial cells; this effect may subsequently regulate the development and progression of intestinal cancer (114). Then, neutral SMase 2 (nSMase2) is encoded by SMPD3 and catalyzes the breakdown of SM to produce ceramide. In mouse models of melanoma and breast cancer, the overexpression of wild-type nSMase2 increases anti-PD-1 efficacy. This increase is associated with an enhanced Th1 response. In wild-type mice, nSMase2-overexpressing tumors accumulate ceramide and CD8+ tumor-infiltrating lymphocytes, which are associated with increased levels of transcripts encoding IFNγ and CXCL9. In vitro, small extracellular vesicles from melanoma cells overexpressing wild-type nSMase2 enhance the expression of IL12, CXCL9, and CCL19 in bone marrow-derived dendritic cells, suggesting that melanoma nSMase2 triggers Th1 polarization at the earliest stages of the immune response (115). This situation suggests that the modulation of sphingolipid metabolism-related enzymes may alter the efficacy of tumor immunotherapy effectively (Figure 4). Hope for the discovery of additional effective targets for modulating tumor immunotherapy has been found with the progression of the research on sphingolipid metabolism-related enzymes in relation to tumor immunity.
Natural products for sphingolipid-based anticancer therapeutics
Natural products medicine has been practiced for thousands of years all over the world and has played an critical role in the treatment and prevention of different diseases throughout history (116). Given their safety and low side effects, natural products are used as alternative cancer therapies. Numerous natural products have various biological activities and low toxicity at the same time and are currently widely accepted as an excellent source of anticancer drugs (117). Previous studies have shown that some herbal compounds can treat and prevent cancer from recurring and metastasizing and can thus prolong the survival of postoperative patients with cancer. When applied in the early stage of cancer, active ingredients can cure pre-cancerous conditions and decrease the rate of cancer occurrence (118). With the transformation of modern medical concepts from treatment to strengthening the physique, the advantages of natural products have become more apparent than before. Thus, as indicated in Table 3, natural products can be used as platforms for the design of sphingolipid-related anticancer drugs.
Many natural compounds isolated from bacteria and fungi possess SPHK inhibition activity. B-5354c, which is produced by a marine bacterium, inhibits SPHK1 and SPHK2 with similar efficiencies (131) and acts on sphingosine in a noncompetitive manner. B-5354c can reduce the size of PC-3 tumors in vivo when combined with the chemotherapy drug irinotecan and can sensitize PC-3 and LNCaP prostate cancer cells to chemotherapy drugs, such as docetaxel and camptothecin (132). B-5354c has been further demonstrated to act as a chemosensitizer of PC-3 cells when used in conjunction with docetaxel (133). F-12509A (125, 126), extracted from Trichopeziella barbata, and S-15183a/b (126), extracted from Zopfifiella inermis, are also natural products that have been found to inhibit SPHK. Jaspine B is an anhydrophytosphingosine, extracted from marine sponge Jaspis sp, with potential antineoplastic property. It can increase the concentration of ceramides within cells by inhibiting SMS. Jaspine B can also induce apoptosis in human SK-Mel28 melanoma and murine B16 cells (127). Myriocin, extracted from Myriococcum ablomyces, specifically inhibits SPT, leading to the suppression of cell growth by triggering the cell cycle in melanoma cells (124) and significantly inhibiting tumor formation in melanoma mice (123). Myriocin combined with docetaxel and cisplatin can also inhibit the growth of cancer cells (120). In prostate cancer, sanguinarine, extracted from Sanguinaria canadensis, Chelidonium majus and Macleaya cordata, inhibits ACDase and GCS enzymes, subsequently resulting in ceramide generation and apoptosis (121).Tricin, a component extracted from rutabaga, exerts proliferation-inhibiting, proapoptotic, and migration-inhibiting effects on Lewis lung cancer cells. It inhibits tumor growth mainly by inhibiting PRKCA/SPHK/S1P signaling and antiapoptotic signaling (73). Resveratrol, extracted from Polygonum cuspidatum Sieb.et Zucc., induces autophagy in gastric cancer cells (HGC-27) by inhibiting dihydroceramide desaturase and increasing dihydroceramide (122). Moreover, resveratrol also triggers anti-proliferative and apoptotic effects in FLT3-ITD-positive acute myeloid leukemia cells through inhibition of ceramide catabolic enzymes (119, 134). Vincristine is a vinca alkaloid that can be obtained from the Madagascar periwinkle Catharanthus roseus (135, 136). The combination of vincristine and SPHK2 inhibitor ABC294640 significantly enhanced the inhibition of SPHK2 and further inhibited the survival and proliferation of T-cell acute lymphoblastic leukemia (T-ALL) cells (129).
Overall, targeting sphingolipid enzymes and altering sphingolipid metabolism can lead to promising anticancer effects. In addition, natural products are a primary source of potential anticancer agents and can thus improve and increase the effectiveness of cancer therapies. The discovery and clarification of their mechanisms of action are urgently needed.
Summary and future perspectives
Sphingolipids have a broad scope of biological functions. Numerous discoveries have elucidated the different roles and mechanisms of sphingolipids in cancers. The unique anticancer or oncogenic functions of sphingolipids in cancers rely on microenvironmental conditions, cell types, and immune status. The rapid metabolism and signaling of sphingolipids within biological membranes have a strong influence on the regulation of cell death and survival. Further studies are needed to determine how sphingolipid enzymes regulate proliferation in cancer systems. Therefore, additional frontier molecular and analytical tools and technologies should be developed and applied in sphingolipid-related anticancer investigations. Although a large number of preclinical trials have shown good results, FDA-approved drugs targeting sphingolipids in cancer treatment remain lacking. Natural drugs, such as TCMs, have made many contributions to the study of sphingolipid metabolism. In the future, strengthening the cooperation in the research and clinical practice of sphingolipids through the integration of Chinese and Western medicine will be necessary and is expected to increase the effectiveness of tumor diagnosis and treatment.
Endogenous ceramides are synthesized through the de novo pathway, which begins with palmitoyl-CoA and the condensation of the amino acid serine to form 3-ketosphinganine via SPT, leading to the synthesis of dihydroceramide by CerS. Dihydroceramides are then converted into ceramides by DES. Ceramides may also be produced through the breakdown of SMs or the degradation of complex sphingolipids under the action of SMase and GCase. In addition, the salvage pathway can generate endogenous ceramides. Sph, a product of sphingolipid breakdown metabolism, can be reanylated by CerS, resulting in the production of ceramides. Once produced, ceramides can briefly accumulate or be converted into different sphingolipids. Ceramides are phosphorylated by CerK to produce C1P and utilized as a substrate by CDase to liberate Sph, which is phosphorylated to generate S1P. Ceramides can also be reversibly metabolized into SM, that is, phosphorylcholine and ceramide generate SM under the action of SMS. GCS can remove ceramides by catalyzing the conversion of ceramides into glycosheath ester. Ceramides can also be converted into GalCer by CGT. (SPT, serine palmitoyl transferase; CerS, ceramide synthases; DES, dihydroceramide desaturase; SMs, sphingomyelins; SMase sphingomyelinases; GCase, glucosylceramidases; Sph, Sphingosine; CerK, ceramide kinase; C1P, ceramide CDase, 1-phosphate; ceramidase; S1P, sphingosine-1-phosphate; SM, sphingomyelin; SMS, phingomyelin synthetase; GCS, Glucoceramide synthetase; GalCer, galactosylceramide; CGT, galactosylceramide transferase.)
Ceramides have antitumor effects but have poor solubility, absorption, bioavailability, and metabolic conversion. Nanoliposomes can help address these disadvantages of ceramides. First, nanoliposomal tamoxifen can enhance the cytotoxicity of nanoliposomal C6-ceramide in TNBC cells, induce cell cycle arrest in the G1 and G2 phases, and increase the permeability of mitochondrial and lysosomal membranes, thus killing TNBC cells. Nanoliposomal C6-ceramide, when combined with PPMP, increases the amount of endogenous long-chain ceramides and increases the apoptosis of leukemic NK cells via the endogenous mitochondrial cell death pathway. Nanoliposomal C6-ceramide reduces the number of TAMs, induces the differentiation of TAMs into the M1 phenotype, increases CD8+ T cell activity, and suppresses the proliferation of hepatocellular tumors. (TNBC, Triple-Negative Breast Cancer; PPMP, [2]1-phenyl-2-palmitoylamino-3-morpholino-1-propanol; TAM, tumor-associated macrophage).
Ceramides activate lysosomal histone B and histone D, leading to the reduction in autophagy and the induction of endoplasmic reticulum stress. These effects further inhibit the function of MDSCs and enhance the activity of cytotoxic T lymphocytes. C2-ceramide up-regulates PKCζ, repolarizes TAM toward the M1 phenotype, increases the activation ratio of CD8+ T cells, and up-regulates the secretion of perforin and granzyme B to kill tumors. S1P induces the conversion of TAM into M2 and promotes the secretion of IL-4, IL-10, and TGFb, thus leading to tumor evasion. (Cer, ceramide; S1P, sphingosine 1 phosphate; MDSCs, myeloid-derived suppressor cells; TAM, tumor-associated macrophage).
Several enzymes are closely related to the effects of tumor immunotherapies. SMase catalyzes the production of ceramide from SM, triggering Th1 polarization, and enhancing anti-PD-1 efficacy. SMase induces ceramide accumulation, thus enhancing the activity of CD8+ tumor-infiltrating lymphocytes and increasing the expression levels of IFNγ, IL12, CXCL9, and CCL19. S1P is catalyzed by SphK directly in relation to the activity of the lipid transcription factor peroxisome proliferator-activated receptor γ, which promotes the lipolysis of T cells. Cer (red) indicates promoted immune killing of tumors, and S1P (green) indicates immunity inhibition, allowing tumors to escape. (Cer, ceramide; S1P, sphingosine 1 phosphate; SMase, sphingomyelinase; Th1, T helper 1; Cers, ceramide synthase; SphK, sphingosine kinase; PPAR γ, peroxisome proliferator-activated receptor γ).
Author contributions
(I) Conception and design: EL-HL, R-ZL, P-YY. (II) Administrative support: LL, EL-HL; (III) Manuscript writing: All authors; (IV) Final approval of manuscript: All authors.
Funding
This work is supported by the 2020 Guangdong Provincial Science and Technology Innovation Strategy Special Fund (Guangdong-Hong Kong-Macau Joint Lab) (No: 2020B1212030006). This work is also supported by Macao Science and Technology Development Fund (Project no: 0096/2018/A3, 0056/2020/AMJ), and from Dr. Neher's Biophysics Laboratory for Innovative Drug Discovery (001/2020/ALC). This work is also supported by 2020 Young Qihuang scholar granted to Prof. Elaine Leung from the National Administration of Traditional Chinese Medicine.
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.
Abbreviations
α-GalCer, α-Galactose ceramide; ACDase, acid ceramidase; ASMase, acid sphingomyelinase; Acer3, Alkaline ceramidase 3; alk-SMase, alkaline sphingomyelinase; CDase, ceramidase; Cer, ceramide; C1P,ceramide 1-phosphate; UGT8, ceramide galactosyltransferase; CerK, ceramide kinase; CerS, ceramide synthase; DES, dihydroceramide desaturase; LASS, dihydroceramidsynthases; PDMP, D-threo-1-phenyl-2-decanoylamino-3-morpholino-propanol; PPMP, D-threo-1-phenyl-2palmitoylamino-3-morpholino-l propanol; FoxP3+, forkhead box protein P3; GlcCer, glucosylceramide; GSLs, glycosphingolipids; GCS, glucosylceramide synthase; LipC6, Nanoliposomal C6-ceramide; NSMase, neutral sphingomyelinase; NSMase2, neutral sphingomyelinase 2; PPAR γ, peroxisome proliferator-activated receptor γ; SPT, serine palmitoyl transferase; SMase, sphingomyelinases; SM, sphingomyelin; SMS, sphingomyelin synthetase; S1P, sphingosine 1-phosphate; SPL, sphingosine 1-phosphate lyase; SphK/SPHK, sphingosine kinase; SPHK1, sphingosine kinase 1; CRC, colorectal cancer; HCC, hepatocellular carcinoma; HNSCC, human head and neck squamous cell carcinoma; iNKT, invariant natural killer T; MDSCs, myeloid-derived suppressor cells; NK, natural killer; Th1, T helper 1 cell; Th2, T helper 2 cell; TNBC, triple negative breast cancer; TAM, tumor-associated macrophage. ER, estrogen receptor; HER2, human epidermal growth factor receptor 2; LN, lymph node; MDR, multidrug resistance; TME, tumor microenvironment; OS, overall survival.
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Keywords: sphingolipid metabolism, enzymes, cancer, immunotherapy, anticancer
Citation: Li R-Z, Wang X-R, Wang J, Xie C, Wang X-X, Pan H-D, Meng W-Y, Liang T-L, Li J-X, Yan P-Y, Wu Q-B, Liu L, Yao X-J and Leung EL-H (2022) The key role of sphingolipid metabolism in cancer: New therapeutic targets, diagnostic and prognostic values, and anti-tumor immunotherapy resistance. Front. Oncol. 12:941643. doi: 10.3389/fonc.2022.941643
Received: 11 May 2022; Accepted: 24 June 2022;
Published: 27 July 2022.
Edited by:
Margarita Ivanova, Lysosomal and Rare Disorders Research and Treatment Center, United StatesReviewed by:
Alberto Ouro, Health Research Institute of Santiago de Compostela (IDIS), SpainAysun Adan, Abdullah Gül University, Turkey
Copyright © 2022 Li, Wang, Wang, Xie, Wang, Pan, Meng, Liang, Li, Yan, Wu, Liu, Yao and Leung. 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: Xiao-Jun Yao, xjyao@must.edu.mo; Liang Liu, lliu@gucm.edu.cn; Elaine Lai-Han Leung, lhleung@um.edu.mo
†These authors have contributed equally to this work