CCL5
癌症研究
体内
转移
趋化因子
肿瘤微环境
化学
前列腺癌
间充质干细胞
体外
生物
医学
癌症
细胞生物学
内科学
细胞毒性T细胞
生物化学
受体
肿瘤细胞
遗传学
白细胞介素2受体
作者
Chiwei Chen,Renlun Huang,Neng Wang,Yifeng Zheng,Jianfu Zhou,Bowen Yang,Xuan Wang,Juping Zhang,Bo Pan,Zhiqiang Chen,Shengqi Wang,Zhiyu Wang,Songtao Xiang
标识
DOI:10.1016/s1875-5364(24)60653-9
摘要
Prostate cancer (PCa) is the second most common malignancy among men globally. The Fu-Zheng-Yi-Liu (FZYL) Formula has been widely utilized in the treatment of PCa. This study investigates whether the FZYL Formula can inhibit PCa by targeting the TAMs/CCL5 pathway. We conducted in vitro co-cultures and in vivo co-injections of PCa cells and TAMs to mimic their interaction. Results showed that the FZYL Formula significantly reduced the proliferation, colony formation, subpopulations of PCSCs, and sphere-formation efficacy of PCa cells, even in the presence of TAM co-culture. Additionally, the Formula markedly decreased the migration, invasion, and epithelial-mesenchymal transition (EMT) of PCa cells induced by TAMs. The FZYL Formula also reversed M2 phenotype polarization in TAMs and dose-dependently reduced their CCL5 expression and secretion, with minimal cytotoxicity observed. Mechanistic studies confirmed that the TAMs/CCL5 axis is a critical target of the FZYL Formula, as the addition of exogenous CCL5 partially reversed the formula's inhibitory effects on PCSCs self-renewal in the co-culture system. Importantly, the Formula also significantly inhibited the growth of PCa xenografts, bone metastasis, and PCSCs activity in vivo by targeting the TAMs/CCL5 pathway. Overall, this study not only elucidates the immunomodulatory mechanism of the FZYL Formula in PCa therapy but also highlights the TAMs/CCL5 axis as a promising therapeutic target.
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