Le Thi Khanh, Duong Quang Hieu, Baylot Virginie, Fargette Christelle, Baboudjian Michael, Colleaux Laurence, Taïeb David, Rocchi Palma
Centre de Recherche en Cancérologie de Marseille-CRCM, Inserm UMR1068, CNRS UMR7258, Aix-Marseille University U105, 13009 Marseille, France.
European Center for Research in Medical Imaging (CERIMED), Aix-Marseille University, 13005 Marseille, France.
Cancers (Basel). 2023 Oct 19;15(20):5047. doi: 10.3390/cancers15205047.
Prostate cancer (PC) is the second most common cancer in men worldwide. Despite recent advances in diagnosis and treatment, castration-resistant prostate cancer (CRPC) remains a significant medical challenge. Prostate cancer cells can develop mechanisms to resist androgen deprivation therapy, such as AR overexpression, AR mutations, alterations in AR coregulators, increased steroidogenic signaling pathways, outlaw pathways, and bypass pathways. Various treatment options for CRPC exist, including androgen deprivation therapy, chemotherapy, immunotherapy, localized or systemic therapeutic radiation, and PARP inhibitors. However, more research is needed to combat CRPC effectively. Further investigation into the underlying mechanisms of the disease and the development of new therapeutic strategies will be crucial in improving patient outcomes. The present work summarizes the current knowledge regarding the underlying mechanisms that promote CRPC, including both AR-dependent and independent pathways. Additionally, we provide an overview of the currently approved therapeutic options for CRPC, with special emphasis on chemotherapy, radiation therapy, immunotherapy, PARP inhibitors, and potential combination strategies.
前列腺癌(PC)是全球男性中第二常见的癌症。尽管在诊断和治疗方面取得了最新进展,但去势抵抗性前列腺癌(CRPC)仍然是一个重大的医学挑战。前列腺癌细胞可以发展出抵抗雄激素剥夺疗法的机制,例如雄激素受体(AR)过表达、AR突变、AR共调节因子的改变、类固醇生成信号通路增加、旁路途径和替代途径。CRPC有多种治疗选择,包括雄激素剥夺疗法、化疗、免疫疗法、局部或全身治疗性放疗以及聚(ADP-核糖)聚合酶(PARP)抑制剂。然而,需要更多研究来有效对抗CRPC。对该疾病潜在机制的进一步研究以及新治疗策略的开发对于改善患者预后至关重要。本研究总结了目前关于促进CRPC的潜在机制的知识,包括AR依赖性和非依赖性途径。此外,我们概述了目前批准的CRPC治疗选择,特别强调化疗、放疗、免疫疗法、PARP抑制剂以及潜在的联合策略。