雄激素受体
前列腺癌
癌症研究
兴奋剂
雄激素受体拮抗剂
雄激素
受体
癌症
雄激素剥夺疗法
恩扎鲁胺
医学
前列腺
内科学
肿瘤科
内分泌学
激素
作者
Raoling Ge,Xi Xu,Pengfei Xu,Lei Li,Zhiyu Li,Jinlei Bian
标识
DOI:10.2174/1568009617666171107103936
摘要
Prostate cancer is the most common carcinoma among aged males in western countries and more aggressive and lethal castration resistant prostate cancer often occurs after androgen deprivation therapy. The high expression of androgens and androgen receptor is closely related to prostate cancer. Efficient androgen receptor antagonists, such as enzalutamide and ARN-509, could be employed as potent anti-prostate cancer agents. Nevertheless, recent studies have revealed that F876L mutation in androgen receptor converts the action of enzalutamide and ARN-509 from an antagonist to agonist, so that novel strategies are urgent to address this resistance mechanism. In this review, we focus on the discussion about some novel strategies, which targets androgen receptor mainly through the degrading pathway as potential treatments for prostate cancer.
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