前列腺癌
雄激素受体
雄激素受体拮抗剂
信号转导
医学
癌症研究
雄激素
受体
癌症
对抗
药理学
抗药性
恩扎鲁胺
肿瘤科
联合疗法
生物信息学
内科学
雄激素剥夺疗法
前列腺
癌症治疗
雄激素抑制
作者
Sara Bleve,Pier Vitale Nuzzo,Abdul Arham,Aaron N. Holmes,Scott T. Tagawa
标识
DOI:10.1080/13543784.2025.2573647
摘要
Novel strategies such as bipolar androgen therapy (BAT), selective androgen receptor modulators (SARMs), and AR degraders like PROTACs offer context-specific or mechanistically distinct ways to overcome resistance to traditional AR antagonism in prostate cancer. These approaches, along with CYP11A1 inhibitors and resistance pathway targeting (e.g. PI3K/AKT, EZH2), mark a shift toward more personalized therapies aimed at improving efficacy while minimizing toxicity.
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