前列腺癌
雄激素受体
雄激素受体拮抗剂
癌症
雄激素
内科学
前列腺
肿瘤科
癌症研究
生物信息学
药理学
医学
化学
生物
激素
作者
Weiguo Xiang,Shaomeng Wang
标识
DOI:10.1021/acs.jmedchem.2c00716
摘要
The androgen receptor (AR) plays a key role in the maintenance of muscle and bone and the support of male sexual-related functions, as well as in the progression of prostate cancer. Accordingly, AR-targeted therapies have been developed for the treatment of related human diseases and conditions. AR agonists are an important class of drugs in the treatment of bone loss and muscle atrophy. AR antagonists have also been developed for the treatment of prostate cancer, including metastatic castration-resistant prostate cancer (mCRPC). Additionally, selective AR degraders (SARDs) have been reported. More recently, heterobifunctional degrader molecules of AR have been developed, and four such compounds are now in clinical development for the treatment of human prostate cancer. This review attempts to summarize the different types of compounds designed to target AR and the current frontiers of research on this important therapeutic target.
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