Title:Recent Developments in Targeting Bromodomain and Extra Terminal
Domain Proteins for Cancer Therapeutics
Volume: 29
Issue: 25
Author(s): Maohua Cai, Jinyun Dong*, Haobin Li and Jiang-Jiang Qin*
Affiliation:
- The Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Institutes
of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou310022, China
- The Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Institutes
of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou310022, China
- School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China
Keywords:
Cancer, BET, BRD4, inhibitor, PROTAC, drug design.
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.