Hou Yifan, Zhao Zhenhua, Li Pan, Cao Yujia, Zhang Yi, Guo Changsheng, Nie Xiaobo, Hou Junqing
Key Laboratory of Receptors-Mediated Gene Regulation, School of Basic Medical Sciences, Henan University, Kaifeng 475004, China; Kaifeng 155 Hospital, China RongTong Medical Healthcare Group Co. Ltd., Kaifeng 475003, China.
Ma'anshan 86 Hospital, China RongTong Medical Healthcare Group Co. Ltd, Ma'anshan 243100, China.
Biochim Biophys Acta Rev Cancer. 2024 Nov;1879(6):189186. doi: 10.1016/j.bbcan.2024.189186. Epub 2024 Sep 25.
The intractability and high mortality rate of castration-resistant prostate cancer (CRPC) remain the most challenging problems in the field of prostate cancer (PCa). Emerging evidence has shown that the dysregulation of Wnt signaling pathways, which are highly conserved cascades that regulate embryonic development and maintain tissue homeostasis, is involved in various stages of PCa occurrence and progression. In this review, we systemically discuss the mechanisms by which the androgen receptor (AR) signaling pathway and Wnt signaling pathways participate in the occurrence of PCa and its progression to CRPC. Specifically, we elaborate on how Wnt signaling pathways induce the malignant transformation of prostate cells, promote the malignant progression of PCa and establish an immunosuppressive prostate tumor microenvironment through interaction with the AR pathway or in an AR-independent manner. We also discuss how Wnt signaling pathways enhances the stemness characteristics of prostate cancer stem cells (PCSCs) to induce the occurrence and metastasis of CPPC. Additionally, we discuss the latest progress in the use of different types of drugs that inhibit the Wnt signaling pathways in the treatment of PCa. We believe that the combination of Wnt signaling-based drugs with endocrine and other therapies is necessary and may enhance the clinical efficacy in the treatment of all types of PCa.
去势抵抗性前列腺癌(CRPC)的难治性和高死亡率仍然是前列腺癌(PCa)领域最具挑战性的问题。新出现的证据表明,Wnt信号通路失调参与了PCa发生和进展的各个阶段,Wnt信号通路是高度保守的级联反应,调节胚胎发育并维持组织稳态。在本综述中,我们系统地讨论了雄激素受体(AR)信号通路和Wnt信号通路参与PCa发生及其向CRPC进展的机制。具体而言,我们阐述了Wnt信号通路如何诱导前列腺细胞的恶性转化,促进PCa的恶性进展,并通过与AR通路相互作用或以AR非依赖的方式建立免疫抑制性前列腺肿瘤微环境。我们还讨论了Wnt信号通路如何增强前列腺癌干细胞(PCSCs)的干性特征以诱导CPPC的发生和转移。此外,我们讨论了使用不同类型药物抑制Wnt信号通路治疗PCa的最新进展。我们认为,基于Wnt信号的药物与内分泌及其他疗法联合使用是必要的,可能会提高治疗所有类型PCa的临床疗效。