溴尿嘧啶
乙酰化
医学
组蛋白
表观遗传学
体内
BRD4
细胞生物学
体外
计算生物学
癌症研究
生物化学
遗传学
生物
基因
出处
期刊:RMD Open
[BMJ]
日期:2018-11-01
卷期号:4 (2): e000744-e000744
被引量:50
标识
DOI:10.1136/rmdopen-2018-000744
摘要
The reading of acetylation marks on histones by bromodomain (BRD) proteins is a key event in transcriptional activation. Small molecule inhibitors targeting bromodomain and extra-terminal (BET) proteins compete for binding to acetylated histones. They have strong anti-inflammatory properties and exhibit encouraging effects in different cell types in vitro and in animal models resembling rheumatic diseases in vivo. Furthermore, recent studies that focus on BRD proteins beyond BET family members are discussed.
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