溴尿嘧啶
BRD4
BET抑制剂
蛋白质水解
计算生物学
癌症
医学
生物信息学
生物
癌症研究
生物化学
表观遗传学
遗传学
酶
基因
作者
Mao-Hua Cai,Jinyun Dong,Haobin Li,Jiang‐Jiang Qin
标识
DOI:10.2174/0929867329666220211091806
摘要
Abstract: Bromodomain and extra-terminal domain (BET) proteins are a well-studied family of proteins associated with a variety of diseases, including malignancy and chronic inflammation. Currently, numerous pan BET inhibitors have exhibited potent efficacy in several in vivo preclinical models and entered clinical trials but have largely stalled due to their adverse events. Therefore, the development of new selective inhibitors and PROTACs (Proteolysis Targeting Chimeras) targeting BET is urgently needed. In the present review, we summarize the BET protein structure and the recent development in BET inhibitors, focusing mainly on BRD4-selective inhibitors and PROTAC degraders.
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