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Targeting Brd4 for cancer therapy: inhibitors and degraders. | LitMetric

Targeting Brd4 for cancer therapy: inhibitors and degraders.

Medchemcomm

Key Laboratory of Advanced Pharmaceutical Technology , Ministry of Education of China , Co-innovation Center of Henan Province for New Drug R & D and Preclinical Safety , Institute of Drug Discovery and Development , School of Pharmaceutical Sciences , Zhengzhou University, 100 Kexue Avenue , Zhengzhou , Henan 450001 , China . Email: ; Email:

Published: November 2018

Bromodomain-containing protein 4 (Brd4) plays an important role in mediating the expression of genes involved in cancers and non-cancer diseases such as inflammatory diseases and acute heart failure. Inactivating Brd4 or downregulating its expression inhibits cancer development, leading to the current interest in Brd4 as a promising anticancer drug target. Numerous Brd4 inhibitors have been studied in recent years and some of them are currently in various phases of clinical trials. Recently, selective degradation of target proteins by small bifunctional molecules (PROTACs) has emerged as an attractive drug discovery approach owing to the advantages it could offer over traditional small-molecule inhibitors. A number of Brd4 degraders have been reported and showed more efficient anticancer activities than just protein inhibition. In this review, we will discuss recent findings in the discovery and development of small-molecule inhibitors and degraders that target Brd4 as a potential anticancer agent.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238758PMC
http://dx.doi.org/10.1039/c8md00198gDOI Listing

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