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Research Trends and Regulation of CCL5 in Prostate Cancer

Authors Huang R, Guo L, Gao M, Li J, Xiang S

Received 28 August 2020

Accepted for publication 20 January 2021

Published 25 February 2021 Volume 2021:14 Pages 1417—1427

DOI https://doi.org/10.2147/OTT.S279189

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Professor Gaetano Romano


Renlun Huang,1,* Lang Guo,1,* Menghan Gao,2 Jing Li,1 Songtao Xiang1

1Department of Urology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, People’s Republic of China; 2Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden

*These authors contributed equally to this work

Correspondence: Songtao Xiang
Department of Urology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, People’s Republic of China
Tel/Fax +86-13711515862
Email [email protected]

Abstract: Prostate cancer (PCa) is considered as the most common cancer of urologic neoplasms, and its development and prognosis are associated with many factors. Chemokine receptor signaling combine with advances in advanced clinicopathological characteristics have provided new insights into the molecular landscape of prostate cancer. Chemokine (C-C motif) ligand 5 (CCL5) is an important member of the CC subfamily of chemokines. The expression of chemokine CCL5 is positively correlated with poor prognostic features in patients with PCa. Current study suggested that CCL5/CCR5 axis plays a significant role in the proliferation, metastasis, angiogenesis, drug resistance of prostate cancer cells and promotes self-renewal of prostate cancer stem cells (PCSCs). Due to the major domination in CCL5 by prostate cancer and the high cancer-specific mortality with prostate cancer, research on the CCL5/CCR5 axis effective antagonists is widespread application. However, challenges for precision oncology of CCL5/CCR5 axis and effective antagonists in CRPC remain. Herein, we summarized the crucial role of CCL5 in promoting the development of PCa and discussed the antitumor application of the antagonists of CCL5/CCR5 axis.

Keywords: chemokine, tumor development, CCR5, antagonists

Introduction

Prostate cancer (PCa), a kind of heterogeneous malignancy, is the most common cancer and the second most common cause of cancer-related mortality among men in the United States, with 174,650 new cases and 31,620 deaths estimated in 2019.1 Regulated by a huge variety of intrinsic and microenvironmental factors, tumor development and malignancy are multifactorial result.2,3 The microenvironmental mediator has become a promising target for PCa treatment.4 Notably, the chemokines, as microenvironmental mediators, are an important messenger mediating the development of PCa.4 For example, CCL5, the abundant chemokine derived from tumor-associated macrophages, can promote PCa metastasis.5 Increased levels of CCL5 in tissues or blood are positively associated with the poor prognosis and advanced clinicopathological characteristics of PCa.5 Accumulating evidences suggest that targeting the CCL5/CCR5 axis can be viewed as an effective antitumor strategy for PCa treatment.5 At present, the antagonists of this axis associated with PCa are cenicriviroc, maraviroc, anibamine and DT-13. These antagonists can exert valid antitumor effects on PCa.

Herein, we review the crucial role of CCL5 in promoting the development of PCa and currently available antagonists that target the CCL5/CCR5 axis for PCa treatment.

Chemokines and CCL5

Chemokines belong to the superfamily of chemotactic cytokines,6 soluble small molecule (8–14 kDa) signaling proteins7 whose receptors are typically seven-transmembrane guanine nucleotide-binding protein (G-protein) coupled receptors (GPCRs).4 The specific binding of chemokines to chemokine receptors will activate the downstream pathway of phosphatidylinositol 3 kinase and small Rho guanosine triphosphatase.8 The first chemokine, platelet factor 4 (PF-4/CXCL4), became known in 1977.9 Since then, chemokines have been identified and divided into four subfamilies: CXC, CC, CX3C, and C chemokines.10 Currently, CXCLn, CCLn, CLn and CX3CLn (L is a ligand, n is a different number) are used to represent different members of the CXC, CC, C, and CX3C families.11 The CC chemokines are known by the two adjacent cysteines at the amino terminus and are closely related to inflammation and the immune response.12 Recent studies have indicated that CCL2213 and CCL514,15 can promote PCa cell migration. CCL5 was originally discovered in 1988 by analyzing cDNA libraries of subtracted T cells,16 but detailed reports on the relationship between CCL5 and PCa were not available until 2004.17 As a member of the CC subfamily, CCL5 is expressed in T lymphocytes, macrophages, synovial fibroblasts, tubular epithelium, endothelial cells, and selected tumor cells, including PCa cells.5,18 It mainly interacts with CCR5 while it can also bind other classic receptors CCR1, CCR3, CCR4 and GPR75 and the atypical receptors ACKR1 and ACKR2 in various cell types.19 When CCL5 recognizes and binds its receptors, such as CCR5, heterotrimeric G proteins and JAK family tyrosine kinases are activated to trigger multiple downstream signaling cascades thus conferring not only the proliferation, metastasis, angiogenesis, and drug resistance of prostate cancer cells, but also the self-renewal of prostate cancer stem cells (PCSCs).5

The Role of CCL5 in the Development of Prostate Cancer

Along with unceasingly thorough research, the occurrence of tumors has been realized to be related to many factors. Chemokines have a wide range of biological functions and are worthy of further study. Among them, CCL5 is the most prominent, for it is not only involved in an inflammatory reaction20 but also closely related to tumorigenesis, tumor growth, invasion and metastasis.2,17 We reviewed existing studies of CCL5 promoting the proliferation, angiogenesis, metastasis, drug resistance of prostate cancer cells and the self-renewal of PCSCs, and which are shown in Figure 1.

Figure 1 The role of CCL5 in PCa. CCL5 promotes PCa proliferation, angiogenesis, metastasis, the formation of stem cells and drug resistance via the crosslinking with CCR5 or CCR1.

Dr. Vaday reported that CCL5 alone could promote the proliferation of PCa cells.21 At the same time, the combination with the CCR5 antagonist TAK-779 inhibited the proliferation of PCa cells, suggesting that CCL5 may act by binding to CCR5.21 There is a research demonstrated that the interaction of the cell surface prostate-specific membrane antigen (PSMA) with specific antibodies strongly induce NF-κB activation and then promote the gene expression of IL-6 and CCL5.22 And CCL5/CCR5 interactions lead to the upregulation of cyclin D1 and ultimately promote the proliferation of LNCaP cells by promoting phosphorylation of STAT5.22 After the addition of CCR5 antibody, cell proliferation was inhibited.22 In addition, CCL5 could also stimulate cell proliferation by activating the mTOR pathway, resulting in rapid upregulation of cyclin D1 and c-Myc.23 The mutual effect between CCL5 and CCR5 could also increase the uptake of glucose, increase ATP production and augment glycolysis in tumor cells, thereby promoting tumor cell proliferation.23

By injecting polyester-polyurethane sponges into mice to induce inflammation, researchers shown that neovascularization was associated with dynamic changes in the chemokine CCL5.24 Furthermore, exogenously added CCL5 in CCR5 knockdown C57BL/6J mice did not promote corneal neovascularization, suggesting that CCL5/CCR5 could promote corneal neovascularization.25 In a study of ovarian cancer, the researcher identified that CCL5 promoted tumor angiogenesis by activating NF-κB and STAT3 pathways.26 After genetic analysis of BPH (Benign Prostate Hyperplasia) cells with CCL5 intervention, the researcher discovered that the expression of angiogenin and pleiotrophin significantly increased, both of which were potent inducers of angiogenesis.27

There are still not enough to uncover the black box of tumor metastasis.28–31 Most research on tumor metastasis has focused on the movement of tumor cells.32,33 It is generally regarded that chemokine signaling pathways promote chemotactic migration. Stuelten describes that when chemokines bind to their receptor, a series of downstream pathways will be activated.34 These include several classical pro-metastatic pathways, such as the PI3K and PTEN pathways.34 With that pathways being activated, cell redistributes the phosphatidylinositol-3,4,5-trisphosphate (PIP3) to the leading edge of cells and harbour pleckstrin homology (PH) domain-containing proteins to the front of cells, and these changes cause actomyosin contraction and tail retraction and finally cause cell migration.23,34,35

CCL5, an important chemokine, promotes the migration and invasion of a variety of tumors, including PCa.36–41 As early as 2003, Vaday et al demonstrated that the invasive ability of PCa cells in the CCL5 experimental group was approximately twice as high as that in the control group, and the effect was weakened after administration of the CCL5 antagonist TAK-779.23 When CCL5 binds to CCR5, as described above, their interaction could also activate the PI3K/Akt pathway, which belongs to the star complex molecular pathway of PI3K-PTEN-mTOR, and the NF-κB pathway, which could promote the secretion of MMP-9 and MMP-2.34,42 In addition, the interaction between CCL5 and CCR5 could also promote metastasis by activating ERK and Rac signaling.34 Notably, Ras oncogenic signaling pathways could activate Jnk signaling pathways, which have been regarded as important signaling pathways in human tumor metastasis.34 And the activated Jnk signaling pathways not only leads to tumor cell proliferation but also promotes tumor metastasis by enhancing the expression of matrix metalloproteinases (MMPs) and reducing the expression of epithelial–mesenchymal transition (EMT) markers such as E-cadherin.43 Moreover, CCL5 could also upregulate MMP-9 by activating STAT3 signaling pathways.44 In other cases, the CCL5/CCR5 axis could promote tumor metastasis by activating MEK or ERK signaling pathways, leading to the activation of αvβ3 integrin.45 Sottnik et al demonstrated that CCL5 derived from a mouse long bone microenvironment could promote metastasis of PCa cells and post-metastasis tumor growth.46 Similarly, Yeh found that cancer-associated fibroblasts (CAF) can secrete IL-6 and CCL5 to recruit macrophages, and then macrophages can promote PCa cells metastasis by secreting IL-6 in the tumor microenvironment.47 Zhao48 illuminated that after co-culture of human umbilical vein endothelial cells (HUVECs) and the CRPC cell line C4-2, CCL5 was the most abundant chemokine in the culture supernatant, and it could enhance autophagy by inhibiting the AR pathway, ultimately reducing cell adhesion and promoting the metastasis of PCa.48 Interestingly, another study found that CCL5 secreted by bone stromal cells could activate the AR signaling pathway which promoting metastasis of PCa cells.49 Karnoub found that CCL5 derived from mesenchymal stem cells could induce a metastatic phenotype and promote tumor metastasis by binding to its receptor CCR5 in primary tumor tissues.41 Furthermore, researchers have noted that distant tumor metastasis is closely related to the intravascular microenvironment, which is the result of the interaction between tumor cells, white blood cells, platelets, and vascular endothelial cells.50 The study finally confirmed that tumor cells could interact with white blood cells and platelets, which could stimulate the microvascular endothelial cells to secrete CCL5, recruiting macrophages to promote tumor metastasis.50 In this study, CCL5 promoted tumor metastasis by changing the tumor metastasis microenvironment rather than directly affecting tumor cells.50 As mentioned earlier, CCL5 can bind to several different receptors and it plays a role in promoting tumor metastasis not only by binding to the major receptor CCR5 but also by binding to the receptor CCR1.18 Interaction between CCR1 and CCL5 could also promote the migration of taxane-resistant prostate cancer cells by activating Rac signaling pathway and by increasing the release of MMP-2 and MMP-9 via the activation of ERK signaling pathway, indicating that CCR1 could be a novel therapeutic target for taxane-resistant prostate cancer.15 Notably, prostate cancer stem cells (PCSCs) play a vital role in PCa metastasis, which is considered as a barrier for successful PCa treatment. For example, Huang demonstrated that CCL5 could promote PCa metastasis via activating β-catenin/STAT3 signaling which is a robustly relevant pathway of cancer stem cells.5

At present, the mainstream understanding is that CSCs is small fractions, approximately 0.1% to 1%, of tumor cells in tumor tissues, with self-renewal and multi-directional differentiation capabilities.51 There is increasing evidence that chemokines could promote the self-renewal of CSCs.52–55 For example, CCL5 could increase the self-renewal of ovarian cancer stem-like cells.56 Studies have found that CCL5 secreted by PC3 and DU145 cells recruited bone marrow mesenchymal stem cells, constituting the tumor immune microenvironment of PCa which promoted the growth, metastasis, and drug resistance of PCa cells.57 Luo et al, via co-culture of bone marrow mesenchymal stem cells and PCa cells, confirmed a new pathway of action named the CCL5-AR-CXCR4/ZEB-1 axis.58 The CCL5 mRNA expression and the secretion of CCL5 were upregulated, which could inhibit AR nuclear translocation and promote the self-renewal of PCSCs.58 Consequently, the activated axis led to the upregulation of ZEB-1, snail and MMP9 and finally promoted the metastasis of PCa.58 Luo et al also showed that CCL5, released by bone marrow mesenchymal stem cells (BM-MSCs), enhanced hypoxia-inducible factor 2α (HIF2α) expression to inhibit AR and HSP90 binding, suppressing nuclear translocation of AR and silencing the androgen receptor (AR) signaling pathways that promote the self-renewal of PCSCs and PCa metastasis.59

In addition, it is necessary to determine the mechanism of tumor drug resistance, which can guide future clinical treatment strategies. When the TLR3 signaling pathway is triggered by DAMPs in HNSCC cells, downstream chemokines, such as CCL5, are activated resulting in resistance to cisplatin.60 In malignant ovarian cancer, cisplatin promoted the secretion of CCL5 by activating cancer-associated fibroblasts (CAFs), and then attenuated the cytotoxic effect of cisplatin on tumor cells.61 It was also found that CCL5 facilitated cisplatin resistance by promoting STAT3 phosphorylation and activating the STAT3 signaling pathway.61 CCL5 could also inhibit apoptosis signaling and promote tamoxifen resistance in breast cancer by promoting STAT3 phosphorylation.62 A study suggested that the treatment with docetaxel promotes the infiltration of CD4+ T cells in PCa tissue, and CD4+ T cells secrete CCL5 to activate STAT3 signaling pathway which promotes PCa Docetaxel resistance.63 CCL5 has been shown to be associated with drug resistance in various tumors. Docetaxel resistance in advanced PCa is a significant factor in treatment failure. So, it is essential to confirm the key role of CCL5 in PCa drug resistance.

The Therapeutic Effect of Drugs on the Action of CCL5/CCR5 Axis in Prostate Cancer

Clinical evidence has indicated that the level of CCL5 in tissues or blood is associated with the poor prognosis of various tumors, including PCa,5 breast cancer,64 gastric cancer65 and so on. By analysing 36 cases of PCa or benign prostatic hyperplasia, König et al identified that CCR5 is elevated in more than 89% of PCa tissues.17 Using GO term analysis, Sicoli et al found that the expression of CCR5 in mouse PCa tissue was 11.3 times higher than that in mouse normal prostate tissue.66 In addition, by consulting the Oncomine database, they found that the expression of CCR5 in patients with PCa was 4 to 5 times higher than that in normal controls, which can also be confirmed by other public databases.66 Through the analysis of clinical specimens of patients, a study found that in the androgen-independent prostate cancer (AIPC) bone metastasis site, the expression of CCL5 was approximately 24 times higher than that of the primary site of PCa.13 Likewise, through analysis of the difference between tumor and non-neoplastic tissues in patients with PCa, several studies demonstrated that the expression of CCL5 significantly increased in stromal cells67 and was approximately 2.31 times than that of normal adjacent tissues.68 According to the analysis of 272 clinical serum specimens, the level of CCL5 in patients with cancerous prostates was approximately 25,323.63 ± 1210.77 pg/mL, which was different from that of patients with non-cancerous prostates as 22,339.28 ± 1185.27 pg/mL (P = 0.080).69 These findings suggest that the CCL5/CCR5 axis has good clinical application prospects as a new therapeutic target and for monitoring or predicting disease development in liquid biopsy. Evaluated in germ-line DNA samples from 814 African-American and Jamaican men by genetic analysis of variant chemokine-associated SNPs, for example, CCR5 gene was linked with a 1.52–1.73 fold increase in PCa risk.70 CCL5/CCR5 inhibitors could exert their antitumor effects.21,66

The current drug development focused on the CCL5/CCR5 axis is primarily directed at CCR5. And the importance of CCR5 in HIV infection has led to the development of compounds that target CCR5.71 Currently, Maraviroc, a marketed drug for CCR5, is primarily used to treat HIV because of its good tolerance, and it is also beneficial in advanced metastatic colorectal cancer.72 As seen from various studies and reviews, antagonists of CCR5 in previous clinical applications are vicriviroc,73 aplaviroc,74 INCB009471,75 cenicriviroc (also known as tako-799),76 PRO140 (Leronlimab),77 anibamine,78 Met-CCL5,79 OTR412080 and OTR4131,80 DT-13,81 and Cenicriviroc TBR-652.82 Herein, the following will focus on CCR5 inhibitors associated with PCa, including cenicriviroc, maraviroc, anibamine and DT-13 which are shown in Table 1.

Table 1 The Therapeutic Effect of Drugs on the Action of CCL5/CCR5 Axis in Prostate Cancer

Maraviroc

Maraviroc, the first-in-class CCR5 inhibitor, was approved by the FDA in 2007 and is used primarily for the clinical treatment of HIV,83 with a 50% inhibitory concentration (IC50) of CCR5 of 5.2 nM.84 Increased expression of CCL5 and CCR5 is associated with metastasis and poor prognosis in PCa.5 Building a stable animal model of bone metastasis contributes to the research of PCa. Sicoli have innovatively established a new stable cell line for the study of PCa bone metastases.66 They utilized v-Src oncogene-transformed prostate epithelial cells and then used these cells to construct a mouse metastasis model, finding that metastasis occurred in all mice.66 They demonstrated that there was a significant difference in the expression of CCR5 between normal mouse prostate tissue and v-Src-PEC subcutaneously implanted tumor tissue.66 At the same time, Src is activated in AKT survival pathway, and is required for CXCLR activation in metastatic cancer, maraviroc prostate cancer metastasis to bone by block CCR5 signaling.66

Cenicriviroc

Cenicriviroc, also called TAK-799, is a CCR5 non-peptide small molecule inhibitor that was first reported in a study on HIV in 1999. With good oral bioavailability and long half-life, its 50% inhibitory concentration (IC50) of CCR5 is 1.4 nM.76 As early as 200621, Dr. Vaday found that TAK-799 attenuated the effect of CCL5 in promoting migration and proliferation of PCa cell lines DU145 and PC3, but the use of TAK-799 alone had no inhibitory effect, which means that other experiments, such as experiments in vivo, are needed to confirm whether it has an effect on PCa.21

Anibamine

Anibamine, the natural product CCR5 antagonist with an IC50 at 1 μM in competition with 125I-gp120, plays a decent role against PCa and provides a structural skeleton for chemical modification of the CCR5 antagonist.85 Studies have found that anibamine could significantly inhibit the proliferation and metastasis of PCa cells by inhibiting CCR5.86,87 Under the full understanding of the structural skeleton of anibamine, Zhang et al constructed 17 anibamine analogues and tested their activity, enhancing the anti-tumor activity of anibamine through structural modification and showing potential for good clinical application of an anibamine antagonist in PCa.88

DT-13

DT-13, as a saponin monomer of dwarf lilyturf tuber,89 has chemical properties and good oral bioavailability compared with similar drugs and inhibits the expression of CCR5 as well as the secretion of CCL5.90,91 A study found that DT-13 has a very comprehensive anti-tumor activity, inhibiting the proliferation, metastasis, and angiogenesis of tumor cells.92 In addition, DT-13 could also augment the role of other antitumor drugs and synergistically enhance the effect of vinorelbine in non-small cell lung cancer92 and the effect of topotecan in gastric cancer,93 for example. The IC50 of PCa cell proliferation inhibition by DT-13 is approximately 5 μM.81 Other studies have shown that DT-13 can inhibit the expression of Integrinβ1 and MMP2/9 and induce apoptosis by blocking the PI3K/Akt pathway, thereby inhibiting the proliferation and migration of PCa cells.81

Regulation of CCL5 Expression and Its Downstream Signaling Pathways

The Transcription Factor Related to CCL5 Expression

The full length of CCL5 gene is 9303 bp, and it is located on chromosome 17q12 by searching in NCBI database.18 It has three transcripts: the 1365 bp CCL5-201, the 1244 bp CCL5-202 and the 719 bp CCL5-203. The transcription factors regulating human CCL5 expression are complex and diverse. Current findings indicated that the CCL5 promoter submodels can be divided into six regions.94,95 Based on previous studies, CCL5 promoter base sequence and binding transcription factor were summarized94,95 and shown in Figure 2. Moreover, there are some bioinformatic strategies to predict the transcription factor of CCL5. Firstly, the base sequence −2000 bp to 100 bp from the CCL5 transcriptional start point was found by analyzing the UCSC database. Secondly, based on the sequence of CCL5 transcriptional start point, the transcription factor regulating CCL5 was predicted through using the PROMO database with 5% fault tolerance, which are shown in Figure 3 plotted via Cytoscape software.96

Figure 2 Model of the regions of the human CCL5 promoter. The regions A to E and G named in order of discovery and their base sequence and binding transcription factor were summarized. The percentages below each region demonstrate the percentage of CCL5 promoter activity remaining after deleting that region.

Abbreviations: NFAT, nuclear factor of activated T cells; PU.1/Ets-1, Ets family members; ATF3, activating transcription factor 3; JunD/FosB/Fra1/Fra2, AP1 family members; R(C)FLAT, R(C) factor of late activated T cells; HMG(γ), high-mobility group protein (γ); IRF-1, interferon regulatory factor-1; GABP, GA binding protein; NF-IL6, nuclear factor of interleukin 6; C/EBP, CAAT/enhancer binding protein; SPBP, stromelysin-1 PDGF responsive element binding protein; NF-ƙB, nuclear factor kappa B; p50/p50, NF-ƙB p50 subunit homodimer; p50/p65, NF-ƙB Rel family members; R(A)FLAT-1, R(A) factor of late activated T cells-1; Sp1, stimulating protein 1.

Figure 3 The transcription factor regulating CCL5 predicted by analysing the UCSC database. We firstly found the base sequence −2000 bp to 100 bp from the CCL5 transcriptional start point and then predicted the transcription factor with the base sequence through using the PROMO database with 5% fault tolerance.

Abbreviations: TBP, TATA-binding protein; TFⅡD, general transcription factor; PITX2, paired-liked homeodo-main transcription factor 2; TCF-4, T cell factor 4; VDR, vitamin D receptor; XBP-1, X-box binding protein-1; YY1, YIN-YANG 1; IK-1, IKaros-1; PR, progesterone receptor; P53, tumor suppressor gene; FOX, Forkhead box; C/EBP, CAAT/enhancer binding protein; AP-2, integrase-type DNA-binding superfamily protein; AR, androgen receptor; Jun/Fos, AP1 family members; Ets-1/Ets-2, Ets family members; C-Myb, MYB proto-oncogene; ER, Leucine-rich receptor-like protein kinase family protein; GATA, Glutamyl-tRNA amidotransferase, subunit A; GR, glutathione reductase; HNF-1A/HNF-1B/HNF-1C, HNF1 homeobox family members; IRF-1, interferon regulatory factor-1; LEF-1, lymphoid enhancer binding factor 1; NF-1, nuclear factor-1; NF-AT, nuclear factor of activated T cells; NF1/CTF, nuclear factor 1 family of site-specific DNA-binding proteins; NF-Y, nuclear factor-Y; Pax-5, paired box 5; PEA3, polymoma virus enhancer 3; PPAR, peroxisome proliferator-activated receptor; PXR/RAR/RXR, nuclear receptor; RelA, RELA proto-oncogene, NF-kB subunit; Sp1, stimulating protein 1; STAT, signal transducer and activator of transcription; T3R-β1, thyroid hormone receptor-beta 1.

The Downstream Pathways of Chemokine CCL5

First, CCL5 can upregulate cyclin D1 expression by promoting phosphorylation of STAT5, which leads to the proliferation of PCa cells.22 Second, CCL5 can promote ovarian cancer angiogenesis by activating the NF-κB and STAT3 pathways.26 Luo et al demonstrated that the CCL5/HIF2α/AR/ZEB-1 axis promotes the self-renewal of PCSCs and PCa metastasis.58,59 CCL5 enhanced hypoxia-inducible factor 2α (HIF2α) expression to inhibit AR and HSP90 binding, thereby decreasing the nuclear translocation of AR, which ultimately leads to the upregulation of ZEB-1.59 Third, Zhao et al illuminated that CCL5 can increase autophagy, which can weaken cell adhesion and further the metastasis of PCa.48 Kato found that the crosslinking of CCL5 and CCR1 activates the RK signaling pathway to promote the release of MMP2/9 and activate the Rac signaling pathway, ultimately facilitate PCa metastasis.15 Moreover, Xiang found that CCL5 can activate STAT3 signaling pathway and that contributes to PCa docetaxel resistance.63 These are summarized and shown in Figure 4.

Figure 4 The schematic diagram of the downstream pathways of CCL5 in PCa. (A) The human umbilical vein endothelial cells (HUVECs), bone stromal cells, macrophages and cancer-associated fibroblasts (CAF) can promote PCa cell metastasis by secreting CCL5 in tumor microenvironment. (B) By secreting CCL5, bone marrow mesenchymal stem cells (BM-MSCs) promote PCa metastasis and stemness. (C) By secreting CCL5, PCa recruit mast cells which can release FGF-2, VEGF and IL-6 to promote angiogenesis. (D) CCL5 promotes the proliferation of prostate cancer. (E) CCL5 promotes the drug resistance of prostate cancer.

Conclusion

This review clarifies the role of CCL5 in PCa and the development made in CCL5 research. The chemokine CCL5 activates a series of downstream pathways through specific binding to the CCR5 receptor. CCL5 plays an important role in tumor growth, metastasis, angiogenesis, tumor resistance, and self-renewal of tumor stem cells. As a key factor that promotes tumorigenesis and tumor development, CCL5 is regulated by multiple elements. Some drugs can reduce the expression of CCR5 and the secretion of CCL5, thus exerting effective antitumor activity. The CCL5/CCR5 axis has a quite broad tumor-promoting effect. And its antagonists are prospective for clinical application which is worthy of further study.

Funding

This work is supported by the National Natural Science Foundation of China (No. 81774067) and Specific Research Fund for TCM Science and Technology of Guangdong Provincial Hospital of Chinese Medicine (YN2016MJ03).

Disclosure

The authors report no conflicts of interest in this work.

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