Emerging roles of and therapeutic strategies targeting BRD4 in cancer

被引:101
作者
White, Mary E. [1 ]
Fenger, Joelle M. [2 ]
Carson, William E., III [3 ,4 ]
机构
[1] Ohio State Univ, Coll Vet Med, Dept Vet Biosci, Columbus, OH 43210 USA
[2] Ohio State Univ, Coll Vet Med, Dept Vet Clin Sci, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Surg, Wexner Med Ctr, Div Surg Oncol, Columbus, OH 43210 USA
[4] Ohio State Univ, James Comprehens Canc Ctr, Columbus, OH USA
关键词
Bromo- and Extra-Terminal (BET) protein family; BRD4; Inflammation and cancer; BET inhibitors; BET BROMODOMAIN INHIBITOR; NF-KB; INFLAMMATION; MYC; SUPPRESSES; PROTEINS; GROWTH; MECHANISMS; ADIPOSITY; THERAPIES;
D O I
10.1016/j.cellimm.2019.02.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Bromodomain and Extra-terminal (BET) family of proteins were first recognized as important epigenetic regulators in inflammatory processes; however, there is increasing evidence to support the notion that BET proteins also play a critical role in 'reading' chromatin and recruiting chromatin-regulating enzymes to control gene expression in a number of pathologic processes, including cancer. To this end, the mechanisms by which BET proteins regulate chromatin remodeling and promote tumor-associated inflammation have been heavily studied over the past decade. This article to review the biology of BET protein dysfunction in promoting tumor-associated inflammation and cancer progression and the application of small molecule inhibitors that target specific BET proteins, alone or in combination with immunomodulatory agents as a novel therapeutic strategy for cancer patients.
引用
收藏
页码:48 / 53
页数:6
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