恩扎鲁胺
前列腺癌
雄激素受体
雄激素剥夺疗法
医学
肿瘤科
内科学
癌症
癌症研究
敌手
受体
作者
Zeyuan Zheng,Jinxin Li,Yankuo Liu,Zhiyuan Shi,Zuodong Xuan,Kunao Yang,Chunlan Xu,Yang Bai,Meiling Fu,Qiaohong Xiao,Huimin Sun,Chun-Kui Shao
出处
期刊:Cancers
[MDPI AG]
日期:2022-10-05
卷期号:14 (19): 4877-4877
被引量:9
标识
DOI:10.3390/cancers14194877
摘要
Prostate cancer (PCa) has the second highest incidence of malignancies occurring in men worldwide. The first-line therapy of PCa is androgen deprivation therapy (ADT). Nonetheless, most patients progress to castration-resistant prostate cancer (CRPC) after being treated by ADT. As a second-generation androgen receptor (AR) antagonist, enzalutamide (ENZ) is the current mainstay of new endocrine therapies for CRPC in clinical use. However, almost all patients develop resistance during AR antagonist therapy due to various mechanisms. At present, ENZ resistance (ENZR) has become challenging in the clinical treatment of CRPC. AR splice variant 7 (AR-V7) refers to a ligand-independent and constitutively active variant of the AR and is considered a key driver of ENZR in CRPC. In this review, we summarize the mechanisms and biological behaviors of AR-V7 in ENZR of CRPC to contribute novel insights for CRPC therapy.
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