Sec. Pharmacology of Anti-Cancer Drugs
Volume 9 - 2019 | https://doi.org/10.3389/fonc.2019.01104
Therapeutic Strategies Targeting Cancer Stem Cells and Their Microenvironment
- 1Department of General Surgery, Cancer Metastasis Institute, Institutes of Biomedical Sciences, Huashan Hospital, Fudan University, Shanghai, China
- 2Medizinische Klinik und Poliklinik IV, Ludwig-Maximilian-University (LMU), Munich, Germany
Cancer stem cells (CSCs) have been demonstrated in a variety of tumors and are thought to act as a clonogenic core for the genesis of new tumor growth. This small subpopulation of cancer cells has been proposed to help drive tumorigenesis, metastasis, recurrence and conventional therapy resistance. CSCs show self-renewal and flexible clonogenic properties and help define specific tumor microenvironments (TME). The interaction between CSCs and TME is thought to function as a dynamic support system that fosters the generation and maintenance of CSCs. Investigation of the interaction between CSCs and the TME is shedding light on the biologic mechanisms underlying the process of tumor malignancy, metastasis, and therapy resistance. We summarize recent advances in CSC biology and their environment, and discuss the challenges and future strategies for targeting this biology as a new therapeutic approach.
Cancer remains one of the leading causes of death worldwide (1). Tumor malignancy is linked to tumor heterogeneity, which has been proposed to be driven by a minor subpopulation of cancer cells referred to as cancer stem cells (CSCs) (2, 3). This subpopulation of tumor cells have the capacity to sustain tumorigenesis and drive tumor heterogeneity, processes that underlie tumor progression, metastasis, and resistance to anti-cancer therapies (4). To date, CSCs identification has been largely based on surface markers as well as their ability to self-renew and propagate. However, CSC surface markers alone are not a reliable means of identifying these populations which has led to some confusion and controversy in the field. It is unlikely that these methods can afford a universal specific marker for the identification of these cells. However, some functional markers including the ATP-binding cassette (ABC) transporter and aldehyde dehydrogenase (ALDH) activity (5), the activation of some key signaling pathways (6), live-cell RNA, and single-cell DNA detection (7) have been found to improve CSCs identification in some instances.
The self-renewal potential and extensive clonogenic properties of CSCs are dependent on the tumor microenvironment (TME) (8, 9). The interaction between CSCs and their tumor niche is strongly linked to the characterization of CSCs (10). Through this interaction, CSCs are able to preserve the tumor heterogeneity that underlies the important malignant behaviors of invasion, metastasis, and therapy resistance (11). The influence of TME on CSCs physiology has been shown to act through intrinsic and extrinsic actions. The intrinsic mechanisms include DNA methylation or demethylation, and gene mutation, while the extrinsic actions involve the production of diverse growth factors and cytokines by the TME leading to the activation of specific signaling pathways (12). In addition, many studies have shown that CSCs may be responsible for tumor resistance to conventional cancer therapy (4, 13). The resistance that is enhanced through the cross-talk between CSCs and the TME include activation of the DNA repair system (8, 14), increased resistance to hypoxic environments (15), and the phenomenon of epithelial to mesenchymal transition (EMT) (16). These features may help explain the therapeutic failures that are often encountered in different tumor settings.
Despite the enormous challenges seen, a series of promising new therapeutic approaches based on this biology are currently under development. Notably, targeted therapeutic approaches have emerged as important tools in treatment strategies. To this end, both the CSCs and the TME represent important therapeutic targets. Emerging research has shown that CSC-targeted approaches have proven to be effective in prolonging survival time (17). In this review, recent advances in CSC biology are summarized, and the potential challenges and future strategies for targeted therapy and combination therapy to eliminate both cancer and CSC populations are discussed.
Identification of CSC
CSCs are a small subpopulation of cells with characteristics that include the capacity to cycle slowly, self-renew, and initiate a novel tumor (18–20). Leukemic stem cells (LSCs) were first described in acute myeloid leukemia (AML), where it was demonstrated that CD34+CD38− AML include a subpopulation of LSCs with a capacity to differentiate and self-renew (20). The early study first demonstrated the existence of a unique tumor subpopulation with the ability to drive tumor progression and recurrence. CSC-like subpopulations have been subsequently isolated from a variety of solid tumors (21). Because some CSCs have been identified via specific surface markers, a door has been opened for potential targeted therapy approaches directed against these cells (22). However, because of the wide diversity underlying this general biology across tumor types, general markers for the global identification of these cells are not available.
The functional relevance of surface markers for CSC identification is still disputed (23, 24). It is suggested that CSCs may arise from normal stem cells, progenitor cells, or even more differentiated cells. In tumor patients, the expression of CSC surface markers in normal organs implies potential metastasis and poor prognosis (25). CD24, CD26, CD44, CD133, CD166, and EpCAM (epithelial cell adhesion molecule, CD326) are surface markers commonly used in CSC characterization (26). CD133 is a special marker that has been widely used for identifying CSCs in different tumor settings (27), especially in solid tumors, such as prostate (28), pancreas (29), brain (30), liver (31), colorectal (32), ovarian (33), osteosarcoma (34), and lung cancer (35). In colorectal cancer, a subpopulation of cells expressing CD133, which comprise 1% of the tumor cells, was shown to efficiently induce xenografts in vivo (36). However, CD133 expression appears to represent only one subset of CSCs and the surface marker can also be found to be ubiquitously expressed on many differentiated cells (37). EpCAM is expessed by most adenocarcinomas and is thought to participatein tumor progression (38). In liver and pancreatic cancer (29, 39), a high expression of EpCAM is associated with the dedifferentiation of tumor cells that have regained stem cell-like features. CD24 is highly expressed in embryonic stem cells (40) and has been widely detected in different tumor settings. The combined surface markers C44/CD24 have been used to identify CSCs in breast tumors (41, 42). CD26 (dipeptidyl peptidase-4, DPP4) is expressed on various cell types, which includes cells with stem traits and is thought to influence progenitor cell migration (43). CD26 is widely detected in leukemic and colorectal cancer (44). Aldehyde dehydrogenase 1A1 (ALDH1A1) has also been identified as a potential CSC marker. ALDH expression is associated with the oxidation of aldehydes to carboxylic acid. ALDH activity has proven useful for the prediction of poor tumor outcome in prostate, breast and lung cancer (45, 46). The ABC transporters are able to pump chemotherapy agents out of the cells that express these proteins. These transporters are widely expressed by CSCs and are thus thought to represent an important component for the failure of cancer chemotherapy. The expression of ABC transporters has been used to identify or isolate CSCs from solid tumors (47). Importantly, CSCs have also been functionally identified in what would represent CSC negative populations based on surface markers (48). Thus, it is generally important to make use of multiple markers to more reliably identify CSCs. To this end, the activation of CSC-related signaling pathways such as the canonical Wnt pathway, has been shown to provide an addition level of information to better identify CSCs from colon and ovarian cancer (49).
Some surface markers used to characterize CSCs are also expressed by normal stem cells. CD29 (integrin β1) is widely expressed on CSCs and also on some normal cells, and is regarded as a marker for breast cancer CSCs. CD29 is important for breast cancer cell adhesion to extracellular matrix, and is thought to promote self-renewal and chemoresistance (50). CD9 (MRP-1) is widely expressed in normal tissues. However, it can also act as an effective marker to diagnose B-acute lymphoblastic leukemia (B-ALL) and is linked to drug resistance. CD44s is frequently used as a CSC marker (51). CD44 is composed of different subtypes (CD44V1-V10) (52, 53) and is expressed by both CSCs and normal cells. CD44 expression is associated with cancer progression and metastasis (51). For example, the CD44V9 is a predictive marker in solid tumors, including head and neck squamous carcinoma and gastric cancer. CD44V3 and V6 have been shown to be linked to invasion, metastasis, and resistance to apoptosis in colorectal cancer (54). The CD44V3-7 varients are highly expressed in non-small cell lung carcinoma (NSCLC) (55, 56). In addition, CD44V6 is associated with lymph node metastasis (6). In examples of breast cancer, high expression of CD44V3, V5, and V6 have been detected and shown to be related to the invasive properties of the tumor (57, 58). ABCB5 (ATP-binding cassette transporter) is a member of the ATP-binding cassette transporter family. ABCB5 expressed by normal cells and contributes to cell proliferation and differentiation (59). However, the expression of ABCB5 has also been demonstrated in several malignant stem cells, including ocular surface squamous neoplasm (OSSN) (60) and melanoma (61, 62). The ABCB5 subpopulation was shown to have an unlimited self-renewal potential, and is thought to foster tumor progression, metastasis, and therapy resistance (63, 64).
CSCs with unlimited self-renewal potential express potential specific markers that can help dinstinguish them from other cells. By making use of markers in CSCs, it may be possible selectively eradicate CSCs in various tumors (22, 65). While there is a growing list of markers that have been used for identification and isolation of CSCs, very few reliable specific surface markers have been found that clearly identify CSCs because CSCs, for the most part, are heterogeneous. The identification of more universal CSC markers across diverse cancer types would clearly redine the field. Finally, what is emerging is that the application of multiple markers used in combination represents the most reliable means of characterizing these cells absence the functional criteria used to define CSCs.
Accumulating evidence suggests that cancer cells acquire a “stemness” feature in part through environment input. Because of this, even differentiated cancer cells can revert to a more dedifferentiated state which has been linked to the ability to form tumors (66). CSCs co-injected into mice with stromal cells extracted from a tumor environment form more aggressive tumors that do CSCs alone suggesting an important role for the stromal matrix surrounding CSCs, also known as the “CSC niche” (67, 68). Cancer cells in a such a niche are capable of maintaining their stemness state (12, 69). The niche can contain various cell types and growth factors providing a tumor promoting microenvironment. This can involve endothelial cells, immune cells, cancer associated fibroblasts (CAFs), various growth factors, and cytokines. In addition to these components, environment changes, such as hypoxia, and pH have been proposed to contribute to the CSC niche (70–72). The perivascular niche, which is best studied in brain tumors, is recognized as a hallmark of glioblastoma (GBM). The perivascular niche enhances GBM stemness and ability for self-renewal and invasion (73).
Low levels of oxygen, referred to as hypoxia, is an important feature of TME. Hypoxia appears to help drive the maintenance of stemness and thus malignancy of CSCs, which promotes tumor survival and metastasis (74). The hypoxia-inducible factors (HIFs) are transcription factors that are increased in response to t hypoxia, and high expression of HIFs (HIF-1α, HIF-2α) is correlated with tumor malignancy (75). The octamer-binding transcription factor 4 (Oct4) is activated by HIF-2α and is linked to control of CSCs self-renewal and an increase in the malignant potential of embryonic stem cell-derived tumors (76). Another transcription factor-Sox2 is also linked to stemness through modulation of Oct4 levels in CSCs (77). A reduction in miR-145 was shown to significantly reduce expression Oct4 and Sox2, and thus lead to a decrease in the CSCs population and chemosensitivity in colon cancer (78). In pancreatic ductal adenocarcinoma (PDAC), YAP/HIF-1α signaling is activated by HGF stimulation through its receptor cMET (79). Dysregulation of YAP is related to tumor proliferation, epithelial mesenchymal transition (EMT) and therapy resistance. In the context of a low oxygen environment, CSCs can obtain energy by both OXPHOS and glycolysis activity. During hypoxia, glycolytic enzymes and glucose transporters become induced by HIF-1. Pyruvate dehydrogenase kinase 1(PKD1) plays a role in converting pyruvate to acetyl-coenzyme A (80). As an essential glycolytic enzyme, PDK1 is associated with tumor proliferation, metastasis and poor prognosis (81). In breast cancer, PDK1 stimulates glycolytic activity to stimulate cancer cells to take on stemness traits (82). The use of PDK1 inhibitors can help block glycolysis activity and also limit maintenance of breast cancer stem cells (82). In many instances, CSCs have been shown to be primarily glycolytic, or to preferentially shift from OXPHOS to glycolysis in a tumor type-dependent manner. In lung cancer (83), glioblastoma (84), and PDCA (85), CSCs were also shown to utilize OXPHOS as the preferred energy production process, however, the mechanism is still unclear. To target this metabolic biology it is thought that a combined therapy targeting both aerobic glycolysis and OXPHOS dependent cells may be the most effective therapy to block CSCs.
CAFs, as a part of TME, are believed to drive tumor progression and dedifferentiation by their secretion of key growth factors and their interplay with other stromal cells. HGF secreted by CAFs was found to activate the canonical Wnt pathway and promote cancer cells to dedifferentiate to the CSCs state (26). Cytokines secreted by CAFs, such as CCL2, IGF-1, and TGF-β affect the expansion and self-renewal of CSCs in breast, lung and gastric cancer (86, 87). In a hypoxic environment, CD44 is highly expressed by CAFs that in turns helps mediate cancer cell migration and stemness sustainability (88). The high-mobility group box 1 (HMGB1) released from CAFs was demonstrated to stimulate CSCs through the TLR4 receptor in breast cancer (89). CAFs induced expression of Notch3 is responsible for the activation of lysine demethylase 1 (LSD1) in CSCs, driving self-renewal in HCC (90, 91). In addition, CAFs facilitate tumor cells migration and metastasis indirectly through EMT. In prostate cancer, CAFs secret CXCL12 and promote EMT by inducing the expression of CXCR4 (one of the EMT phenotypes), which enhances metastasis (92). Recent reports also show that CSCs can differentiate into CAF-like cells through TGF-β secretion that promotes self-renewal and proliferation (93). CSCs also secret the Hedgehog ligand SHH that is known to increase the proliferation of CAF in the mammary tumor, and the CAFs secret factors to improve the ability of CSCs malignancy (94).
The biological cross-talk between CSCs and TME is quite complicated, and changes between different tumors and environments. By better understanding these processes, we can develop novel strategies to better target CSCs. Figures 1, 2 gives insight into illustration of hypoxia and CAF interactions on CSC.
Figure 1. Schematic illustration of the potential effects of hypoxia interaction on cancer stem cells (CSCs).
Figure 2. Schematic illustration of the potential effects of CAF interaction on cancer stem cells (CSCs).
Therapeutic Resistance Driven by CSC and their Microenvironment
Tumors recurrence often means poor prognosis and increased resistance to therapy (95, 96). Increasing evidence suggests that the interplay between CSCs and their TME is important in tumor development. The tumor is a complex tissue composed of different subpopulations of tumor cells and tumor-associated stromal cells. Through interaction with the microenvironment, CSCs can avoid target exposure and this may be a key to therapy resistance (97–99).
The general therapeutic resistance of CSCs allows them to escape from elimination and re-establish tumor. When the treatment cycle comes to an end, CSCs are revived from their quiescence and promote tumorgenesis (100, 101). The mechanisms by which CSCs achieve therapeutic resistance involves heightened DNA damage repair capacity, high expression of multiple drug resistance (MDR) transporters and high expression of anti-apoptosis proteins (102–105).
The DNA damaging repair (DDR) system is important in tumor progression. When under chemotherapy or radiotherapy, damaged DNA triggers the DDR, which enables CSCs to survive and thereby remain resistent to treatment. Several pathways can be activated in cancer cells includiong the double-strand breaks (DSBs) repair (homologous and non-homologous end joining), base excision repair (BER), transcription coupled nucleotide excision repair (NER), and mismatch repair (MMR) systems (106). Previous study have showen that the high expression of apurinic/apirimidinic endonuclease/redox effector factor (Ape1/Ref-1), corresponding to an activation of the BER pathway, has been implicated in the development of CSCs (107). Overexpressed Ape1/Ref-1 was also shown to maintain a low level of reactive oxygen radicals (ROS) that prevented DNA damage and cell death in CSCs (108–110). The Mre11-Rad50-Nbs1 (MRN) complex has the capacity to repair DNA and modulate cells apoptosis, and gene stability and is an important part in the DSBs pathway (111, 112). In nasopharyngeal and gastric cancer, MRN-ATM meditated DNA repair induced resistance to common chemotherapy agents, such as cisplatin and 5-FU (113, 114). The MRN complex also acts as one of the DSB pathway key elements to produce radio-resistance in various cancer types (115). Transcription factors such as forkhead box protein m1 (FOXM1), P53, glioma-associated oncogene (GLI1), and c-MYC, were also shown to be important for the DNA repair response (116, 117). Treating colon cancer with doxorubicin (a chemotherapy agent) was shown to lead to the activation of SMAD, which binds to P53 to produce chemoresistance (118).
The expression of multi-drug resistance (MDR) transporters in CSCs results in drug efflux and decreased intracellular drug concentration (119, 120). The ATP-binding cassette (ABC) transporters encompass 49 members in humans and are organized into seven subfamilies (ABCA-G) (121, 122). Three well-studied members of the family are ABCB1, ABCG2, and ABCC1 (123, 124). Overexpression of ABCG2 is associated with resistance to a large number of chemotherapy agents, such as mitoxantrone, camptothecins and flavopiridol (125). The human breast cancer resistance protein (BCRP/ABCG2), which was derived from the breast cancer cell line Mcf-7, was shown to induce resistance to mitoxantrone (126, 127). However, this resistance could be reverted by the MiR-487a target for the expression of BRCP (126). In ovarian cancer, c-MET/PI3K/AKT pathway activation was shown to induce the expression of BRCP/ABCG2, which is important in doxorubicin resistance (125, 128). ABCB1 is also called P-glycoprotein (P-gp) or multidrug resistance gene 1 (MDR1). In AML, P-gp acts as an adverse prognostic factor for drug resistance (129). It was also found that the absence of miR-298 is related to an over expression of P-gp. The upregulation of miR-298 could reduce the expression P-gp, leading to increased concentration and cytotoxicity of doxorubicin in doxorubicin-resistant breast cells (130). In addition, oncogene kinases such as MEK1/2, ERK1/2, c-Raf, EGF, and FGF, can increase the expression of P-gp and effect drug resistance and therefore may also represent potential targets (131). The ACBC1 transporter is encoded by the MRP1gene. This subfamily plays a role in affecting MDR in lung, bladder, and breast cancer (124). In neuroblastoma, the high expression of MRP1 is associated with a poor outcome and sensitivity to chemotherapy should be regained by targeting MRP1 (132).
Hypoxia influences cancer progression, and therapy resistance, and it leads to poor outcomes. The ROS level is affected by oxygen density. In tumors, hypoxia leads to a low ROS level that in turn can be protective for CSCs and lead to therapy failure (133). HIFs are considered as negative factors for effective tumor therapy. It has been suggested that HIFs influence the pathways that contribute to the quiescence of CSCs, such as cell cycle control via cyclin dependent kinase, metabolic control via pyruvate dependent kinase, anti-apoptosis via BCL-XL, and self-renewal via OCT-4 (134–136). In some reports, HIFs are believed to be related to MDR, such as ABCG2, and to affect drug efficacy. VEGF has also been proven to be induced by hypoxia, leading to chemo/radiotherapy resistance (137, 138). In colon cancer, dual specificity phosphatase-2 (DUSP-2) was suppressed by hypoxic culture, which led to the upregulation of COX-2 expression. DUSP-2 has a negative function in cancer malignancy and COX-2 is closely related to cancer stemness, tumor growth and drug resistance (139).
Anti-apoptosis protein expression in CSCs is another component of therapy resistance. BCL2 and BCL-XL are highly expressed in breast and AML CSCs (136, 140). P53 is a tumor suppressor that is frequently mutated in most human cancers. Due to programs such as inactivation of caspase-9 and protease activating factor1 (Apaf-1), and the activation of gain-of-function, the mutant P53 shows acquisition of dedifferentiation and stemness that leads to drug resistance (141, 142). An altered apoptosis pathway has also been demonstrated to be involved in the formation of drug resistance. The high expression of Bcl-2 due to Notch and Hh signaling pathways translates into docetaxel resistance in prostate CSCs (143). Additionally, Hh signaling pathway activation in AML, especially in CD34+ leukemic cell lymphoma, induces the function of anti-apoptosis that lead to chemotherapy (144).
EMT activities in the CSC environment include wound healing, tissue fibrosis, and carcinoma progression. Non-small lung cancer (NSCLC) treated with Erlotinib targeting EGFR mutation shows more drug resistance due to mesenchymal-like expression. With the reversion of EMT, an elevated epigenetic like the expression of E-cadherin, is associated with sensitivity to the EGFR kinase inhibitor (145). It is generally accepted that the Notch pathway is associated with gemcitabine resistance in PDAC and is regulated by EMT (146). The expression of mesenchymal-like regulators such as Zeb2/SIP1 can protect cells from DNA damage-induced apoptosis in bladder cancer, leading to poor prognosis (147). In non-small lung cancer (NSCLC), EMT is thought to act in the process of quiescence. Overexpressed CSC surface markers, such as ALDH1 and CD133 in NSCLC stem cells are proposed to develop resistance to conventional therapy agents 5-FU (148). CSC-mediated therapeutic resistance relies on different mechanisms. Figure 3 gives insight into illustration of therapeutic resistance driven by CSC and microenvironment.
Figure 3. Schematic representation of cancer stem cells (CSCs) and its role in therapeutic resistance. (A) Most of the cancer cells are eliminated by therapeutic resistance. CSC could escape from chemotherapy and re-establish tumor. (B) CSC possess several mechanisms to achieve therapeutic resistance involves Hypoxia environment, high expression of anti-apoptosis proteins, epithelial mesenchymal transition (EMT), DNA damaging repair system (DDR), multiple drug resistance transporters (MDR).
Therapeutic Strategies Targeting CSC and their Microenvirements
CSC Targeting Strategies
The selective targeting CSCs is a promising therapeutic strategy to eliminate the development of human cancer and reduce the risk of recurrence (149). Therapeutic strategies discussed include disrupting the central regulating signaling pathways important for the cell type, targeting specific markers, inhibition of the ABC transporters, manipulating miRNA expression, or inducing the differentiation and apoptosis of CSCs.
Signaling pathways that underlie CSC biology and have been identified as potential targets. Key pathways identified include Sonic hedgehog (Shh)/Patched (Ptch)/Smoothened (Smo), Notch/Delta-like ligand (DLL), CXC chemokine receptor 1-2/CXCL8/FAK, and Wnt pathways. Downstream transcription factors such as β-catenin, STAT3, and Nanog have also been identified as potential clinical targets (150). However, the fact that CSCs and normal stem cells share the expression of many genes and signaling pathways, as well as the redundancy of the regulatory pathways, may effectively limit the efficacy and clinical impact of the therapeutic approaches.
Drugs targeting CSC markers may play an adjunctive role together with surgery, chemotherapy, and radiotherapy (151). CD44, the transmembrane protein that is the receptor for matrix components such as hyaluronic acid selectin, collagen, and osteopontin, has been proven to help treat acute myeloid leukemia (AML) by inhibiting tumor proliferation, and increasing apoptosis (152, 153). CD133, the glycoprotein also known as prominin-1, is another well-known marker on the CSCs surface and it has been reported to be a useful target in cancers with a large CD133 subpopulation (154, 155). In addition, other drugs approved by FDA are also used for targeting CSC markers such as rituximab (anti-CD20) (156), cetuximab (anti-EGFR) (157–159).
The aberrant expression of ABC transporters, which are drug efflux pumps, is a major mechanism of chemoresistance in CSCs cells (160). Three generations of inhibitor drugs have been developed and the fourth generation is underway (49, 160), which should be more selective and less toxic. New technology has been applied to improve therapy efficacy, such as the application of miRNAs targeting specific RNAs or the use of nanomedicines for bypassing efflux pumps. However, currently no inhibitors have been approved for clinical practice. Accumulating studies have reported that different tyrosine kinase inhibitors (TKIs) including erlotinib, lapatinib, imatinib, and nilotinib can reverse drug resistance mediated by ABC transporters (161). The ability to inhibit the multiple regulatory targets of ABC transporters synergisticly, combined with other therapy strategies to overcome chemoresistance in CSCs may represent a promising approach.
CSCs have non-coding RNA profiles that are different from those seen in other cancer cells. Non-coding RNAs act as regulators in maintaining and modifying CSCs properties and functions (162). As such, they represent not only potential drugs but also therapeutic targets for the treatment of CSCs. Accumulating evidence suggests that non-coding RNAs, including microRNA (miRNA) and long non-coding RNA (LncRNA), regulate the stemness of CSCs by acting as suppressors or promoters of pathways that modulate the CSC carcinogenesis, differentiation, and EMT. In breast CSC and CD133 positive pancreatic cancer cells, miR-30 was found to be decreased and inhibited anoikis resistance (163). Three novel LncRNAs including Lnc TCF7, Lnc-b-Catm, and Lnc BRM were reported to sustain the self-renewal of CSCs by regulating the classic signaling pathways related to development and progression of liver CSC (164). Non-coding RNAs are regarded as very useful targets for potential therapeutic strategies due to their limited and selective expression in tumor tissues. MiRNA-based therapeutics are also emerging as tumor treatment options and are currently entering clinical trials (165). For example, a phase 1 clinical trial that targomiRs, minicells loaded with miR-16-based mimic miRNA and targeted to EGFR, is being evaluated in patients with malignant pleural mesothelioma and non-small cell lung cancer (166).
The impairment of apoptosis contributes to cancer development and progression, and the reactivation of apoptosis programs might be useful in the treatment of cancer. It has been reported that targeting TRAIL could cause caspase-8 reactivation, ultimately initiating mitochondrial outer membrane permeabilization and triggering the apoptosis (167). In PACA, JNK inhibition attenuated resistance of TRAIL-induced apoptosis and reduced the self-renewal capacity of CSCs (168). Finally, inhibition of NF-κB by the molecule MG-132, has also been reported to induce cell death (169). Another approach that has been evaluated focused on various means to induce CSCs differentiation. Promising agents are under research currently include the use of retinoic acid and its analogs (ATRA) for the treatment of promyelocytic leukemia (170–172). These may also show utilityto induce differentiation of glioma and breast CSCs. Other molecules such as histone deacetylase inhibitors (HDACI), tyrosine kinase have also been proposed in many CSCs studies (151). Most recent antibody targets in CSC were summarized in Table 1.
Targeting the CSC Environment
The tumor environment is comprised of various components including CAFs, immune cells, multipotent stromal cells (MSCs), endothelial and perivascular cells, and their secreted factors including growth factors and cytokines. In addition, this environment is made up of extracellular matrix (ECM) components, and extracellular vesicles, within a prevailing hypoxic region (12). The tumor stroma is thought ot help foster the generation and maintenance of CSCs, protect the tumor from the immune system (173), and contribute to the induction of EMT, leading to enhanced tumor progression, invasion, and recolonization as secondary tumors. Furthermore, CSCs can acquire drug resistance by interacting with niche components in TME. Thus, targeting the TME may represent an effective indirect therapeutic strategy for the treatment of CSCs and for the prevention of drug resistance.
Stromal Cells in the CSC Niche
It is recognized that tumor stromal cells can not only provide physical shelter for CSC by limiting drug access, but also promote CSC growth, migration, and metastasis by producing important growth factors, cytokines and chemokines (174). Since the cross-talk between CSCs and stromal cells can stimulate tumor aggressiveness, directly targeting the stromal cells may serve as an alternative therapeutic strategy to treat CSCs (175).
Vascular endothelial cells (ECs), a type of stromal cell in CSC niche, which are required for angiogenesis, can also secrete growth factors and cytokines that enhance the proliferation of cancer cells, and promote the maintenance of CSCs properties in head and neck squamous cell carcinoma (176, 177). Interfering with tumor EC growth and survival could in theory inhibit not only angiogenesis but also the self-replication of CSCs (178). VEGF is a strong proangiogenic factor secreted by cancer cells, that is a well-recognized therapeutic target. Various angiogenic inhibitors have been developed that can also inhibit the self-renewal of CSCs leading to reduced tumor growth. In GBM, the VEGF tyrosine kinase inhibitor—bevacizumab has proven successful in expanding survival time by targeting the perivascular niche (179). Also in GBM, the VEGF-VEGF2-NRP1 axis is seen as an attractive target in order to decrease CD133+GBM CSCs (180). Bevacizumab combined with anti-hepatoma-derived growth factor (HDGF) antibody has been shown to suppress CSC populations in NSCLC (181). However, in breast cancer, inhibition of VEGFR may increase CSCs population by inducing hypoxia (182). To address this it may be that use of a VEGFR inhibitor in combination witt HIF inhibition in combination therapy may provide a more effective treatment strategy (183).
CAFs represent the major component of tumor stroma andalso play an important role in cancer therapeutic resistance and radiotherapy resistance. Thus, the direct targeting of CAFs may enhance clinical outcomes. Surface markers of CAFs such as FAP, S1004A, and TEM8 have been directly targeted through administration of sibrotuzumab, 5C3, and ADC, respectively, in various tumor types (184–186). In breast cancer, CAF activation was blocked by inhibition of Hedgehog (Hh) signaling, which also increased the sensitivity of resident CSCs to chemotherapy agents (187). CAFs secret TGF-β, and the inhibition of TGF-β signaling by using LY364947 administered via nanoparticle therapy showed a potent therapeutic effect by disrupting CSC biology (188). PTK7 as a special marker of HNSCC stem cells and is demonstrated to have a close relationship with tumor persistence, metastasis, and recurrence. The use of a PTK7 inhibitor was found to increase the sensitivity of HNSCC to erlotinib (189). In addition to a direct activity on CSCs, the inhibition of important signaling pathways may represent a prospective strategy in tumor treatment. Notch signaling is over-activated in HCC, and is thought to help maintain stemness in liver CSCs by regulating LSD1 deacetylation in CAFs (190). CD10+GPR77+ CAFs were demonstrated to promote cancer stemness and chemoresistance. An antibody against GPR77 was demonstrated to reverse chemoresistance by targeting the CD10+GPR77+ CAF subset in solid tumors, such as in breast, lung cancer (191).
Tumor-associated macrophages (TAMs), feature M2-like characteristics and are important components of TME. TAMs have been demonstrated to promote CSC immunosuppressive traits leading to immune escape (192). It has been suggested that TAMs may represent potential targets for immunotherapy. In inflammatory breast cancer (IBC), tumor cells interact with immune suppressing M2-TAM leading to the production of high levels of IL-8 and CCL18 chemokines that in turn activate STAT3, which induces a CSCs-like phenotype in IBC cells and drives EMT during IBC progression (193). Targeting CXCL8/GRP/STAT3 may represent a therapeutic choice in the treatment of IBC (194). In lung cancer, the Src kinase is associated with metastasis and stemness (195). For example, it has been demonstrated that overexpressing Src in M2-TAMs induces cisplatin resistance in lung cancer. Inhibition of Src using the small molecular agent dasatinib, was found to re-sensitize lung cancer cells to cisplatin (196). CAF derived CXCL12 can help attract monocytes, which display M2 TAM characteristics. Blocking the CXCL12/CXCR4 axis significantly reduced the effect of M2 TME leading to reduced cell proliferation, migration and resistance to vineristine in OSCC chemotherapy (197). A member of the immunoglobulin family, CD47 is found to be overexpressed on the surface of many cancer types. It binds to the signal regulatory protein alpha (SIRPα) to prevent cancer cells from undergoing phagocytosis in the tumor environment (198, 199). Targeting CD47, or interfering with the CD47-SIRPα axis leads to enhanced tumor phagocytosis by macrophages and represents a promising therapeutic strategy to treat CSCs (200–202). It has been shown in HCC that the miRNA 125 delivered via TAM exosomes may significantly suppress the CSC phenotype and limit drug resistance (203). The same function of miRNA125 or TAM exosomes have also been seen in cervical cancer (204), nasopharyngeal cancer (205), and AML (206).
Immunotherapy is an emerging field and the exact mechanism by which these therapies may abrogate the ability of CSCs to reinitiate tumors is still under investigation. Over the past decade, therapeutic approaches have utilized the cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) (207) or programmed death 1 (PD-1)/programmed death receptor ligand-1 (PD-L1) (208) blocking antibodies, which have yielded notable response rates and have shown a remarkable clinical response in patients with advanced cancer. Despite the recent successes, the utilization of single antibodies is often limited and leads to poor treatment outcome. To achieve improved immune responses, the use of combination strategies for checkpoint inhibitors with other therapeutics may offer a stronger response against cancer as well as higher recovery rates (209, 210). PD-1 blockade was shown to enhance a specific antitumor efficacy of streptavidin-granulocyte-macrophage-CSF surface-modified bladder cancer stem cells vaccine (211). A recent study showed that targeting CSCs using the CSC-dendritic cell vaccine with CTLA-4 and PD-L1 blockades simultaneously enhanced the eradication of melanoma stem cells in the mouse model (212). In addition, CAR-T cells have produced remarkable antitumor activities in different types of tumors (213, 214). In prostate cancer and NSCLC tumor models, CAR T-cells targeted against EpCAM and EGFR antigens could successfully eradicate CSCs and cancer cells (215, 216). Most recent target factors and chemokines in CSC were summarized in Table 2.
Conclusions and Future Perspectives
Based on the central impact of CSCs on tumor progression with accompanying poor patient outcome, CSCs-targeted therapy approaches have emerged as an important new strategy for future tumor treatments. However, the identification of CSCs remains a challenge. Markers expressed on CSCs may also be displayed by normal stem cells, which may limit the accuracy of CSCs identification and compromise the targeted treatment. In addition, CSCs appear to represent by heterogeneous populations within tumor settings. Therefore, CSC surface markers alone are not broadly reliable for their identification. The best results, absence functional criteria, results from the use of multiple markers which provide a better means of identifying CSC in specific tumor types and may provide information regarding potential drug responsiveness and tumor recurrence.
CSCs have been demonstrated to influence tumor metastasis, immune escape, and drug resistance. Targeting CSCs via their unique signaling pathways, by metabolism reprogramming, hitting the ABC transporters, and even the use of non-coding RNA, represent promising strategies to control tumor progression through CSC-based targeting. However, due to the inherent heterogeneity of CSCs the targeting a single molecule or pathway may not be an effective strategy. Combination therapy may represent the most efficient means for the treatment of CSCs.
In cross-talk with CSCs, the tissue environment plays an important role in the development of tumor metastasis and recurrence. In the TME, CSCs are thought to reside in a special “CSC niche,” which helps maintain their self–renewal and stemness. Immunotherapy represents an important emerging field in tumor therapy. Recent impressive results have been seen in immune targeting of CSCs through the use of PD-1/PDL-1 inhibitors. However, some studies have reported that CSCs are less immunogenic than non-CSCs, and thereby limiting antitumor response to CSCs. CAR-T cells also hold promise in overcoming cancer resistance in different types of tumors. Thus, targeting both CSCs and TME may represent the best option in the anti-cancer approach. Although the interconnected networks between CSCs and TME are complex, and most mechanisms are still obscure, various CSC targeting agents have been developed and successfully tested in several tumor types. In contrast with the single focus of CSCs-targeted therapy, because TME components include different types of stroma cells, cytokines, and growth factors, many of them have proved to be targeted in the eradication of CSCs. However, although there is growing literature in this promising area, the therapeutics of targeting CSCs and their environment are still in its infancy. Research on CSCs and their related environments will provide new targets for the development of anti-tumor strategies. In addition, clarifying the interconnectiveness of CSCs and TME will be important for the design of effective therapeutic approaches. The focus of future trials may include combination therapies that target multiple mechanisms in the tumor. However, this field is still undeveloped, and considerable research will be required to produce viable products. Many important challenges remain, including how to achieve drug selectivity and efficacy, reduce toxicity to normal cells, reduce adverse side effects, and explore new approaches to deliver and keep an effective drug concentration in place. In conclusion, the combined regimen of CSC-targeted therapy together with conventional treatment methods shows great potential and deserves further research.
Q-ZD and L-XQ designed and supervised the entire project. H-RS, SW, and S-CY wrote the manuscript. Q-ZD and PN made significant revisions to the manuscript. All authors read and approved the final manuscript.
This work was supported by the following: the National Key Research and Development Program of China (2017YFC1308604); the National Key Basic Research Program of China (2014CB542101 and 2013CB910500); National Natural Science Foundation of China (81672820, 81772563 and 81872356).
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.
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Keywords: cancer stem cells, tumor microenvironments, therapeutic resistance, mechanism, strategy
Citation: Sun H-R, Wang S, Yan S-C, Zhang Y, Nelson PJ, Jia H-L, Qin L-X and Dong Q-Z (2019) Therapeutic Strategies Targeting Cancer Stem Cells and Their Microenvironment. Front. Oncol. 9:1104. doi: 10.3389/fonc.2019.01104
Received: 26 June 2019; Accepted: 07 October 2019;
Published: 24 October 2019.
Edited by:Alexandre Prieur, ECS-Screening SA, Switzerland
Reviewed by:Marco Falasca, Curtin University, Australia
Nor Eddine Sounni, University of Liège, Belgium
Copyright © 2019 Sun, Wang, Yan, Zhang, Nelson, Jia, Qin and Dong. 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: Lun-Xiu Qin, firstname.lastname@example.org; Qiong-Zhu Dong, email@example.com