雄激素受体
前列腺癌
化学
嵌合体(遗传学)
蛋白质水解
受体
斑马鱼
癌症研究
LNCaP公司
前列腺
癌症
雄激素受体拮抗剂
雄激素
药理学
内科学
生物化学
生物
激素
酶
医学
基因
作者
Linrong Chen,Liuquan Han,Shujun Mao,Ping Xu,Xinxin Xu,Ruibo Zhao,Zhihua Wu,Kai Zhong,Guangliang Yu,Xiaolei Wang
标识
DOI:10.1016/j.ejmech.2021.113307
摘要
Androgen receptor (AR) is an effective therapeutic target for the treatment of prostate cancer. We report herein the design, synthesis, and biological evaluation of highly effective proteolysis targeting chimeras (PROTAC) androgen receptor (AR) degraders, such as compound A031. It could induce the degradation of AR protein in VCaP cell lines in a time-dependent manner, achieving the IC 50 value of less than 0.25 μM. The A031 is 5 times less toxic than EZLA and works with an appropriate half-life (t 1/2) or clearance rate (Cl). Also, it has a significant inhibitory effect on tumor growth in zebrafish transplanted with human prostate cancer (VCaP). Therefore, A031 provides a further idea of developing novel drugs for prostate cancer.
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