Fu-Zheng-Yi-Liu Formula inhibits the stem cells and metastasis of prostate cancer via tumor-associated macrophages/C-C motif chemokine ligand 5 pathway in tumor microenvironment

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
出处
期刊:Chinese Journal of Natural Medicines [Elsevier BV]
卷期号:22 (6): 501-514 被引量:5
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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