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前列腺癌第二代抗雄激素治疗耐药机制:现有知识与展望。

Mechanisms of Resistance to Second-Generation Antiandrogen Therapy for Prostate Cancer: Actual Knowledge and Perspectives.

机构信息

Urology Department, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Catholic University of the Sacred Heart, 00168 Rome, Italy.

出版信息

Med Sci (Basel). 2022 Apr 28;10(2):25. doi: 10.3390/medsci10020025.

Abstract

Prostate cancer therapy for locally advanced and metastatic diseases includes androgen deprivation therapy (ADT). Second-generation antiandrogens have a role in castration-resistant prostate cancer. Nevertheless, some patients do not respond to this therapy, and eventually all the patients became resistant. This is due to modifications to intracellular signaling pathways, genomic alteration, cytokines production, metabolic switches, constitutional receptor activation, overexpression of some proteins, and regulation of gene expression. The aim of this review is to define the most important mechanisms that drive this resistance and the newest discoveries in this field, specifically for enzalutamide and abiraterone, with potential implications for future therapeutic targets. Furthermore, apalutamide and darolutamide share some resistance mechanisms with abiraterone and enzalutamide and could be useful in some resistance settings.

摘要

局部晚期和转移性前列腺癌的治疗包括雄激素剥夺疗法(ADT)。第二代抗雄激素在去势抵抗性前列腺癌中具有作用。然而,一些患者对这种治疗没有反应,最终所有患者都产生了耐药性。这是由于细胞内信号通路的改变、基因组改变、细胞因子的产生、代谢转换、受体组成激活、某些蛋白质的过度表达以及基因表达的调控。本文综述的目的是确定导致这种耐药性的最重要机制,以及该领域的最新发现,特别是恩扎鲁胺和阿比特龙的发现,这可能对未来的治疗靶点有潜在影响。此外,阿帕鲁胺和达罗他胺与阿比特龙和恩扎鲁胺有一些耐药机制,在某些耐药情况下可能有用。

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