溴尿嘧啶
BRD4
转录组
表观遗传学
功能(生物学)
细胞生物学
生物
计算生物学
生物信息学
医学
遗传学
基因表达
基因
作者
Soo Young Kim,Xin Zhang,Gabriele G. Schiattarella,Francisco Altamirano,Thaís A. R. Ramos,Kristin M. French,Nan Jiang,Pamela A. Szweda,Bret M. Evers,Herman I. May,Xiang Luo,Hongliang Li,Luke I. Szweda,Vinicius Maracaja‐Coutinho,Sergio Lavandero,Thomas G. Gillette,Joseph A. Hill
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:2020-10-28
卷期号:142 (24): 2356-2370
被引量:62
标识
DOI:10.1161/circulationaha.120.047239
摘要
BET (bromodomain and extraterminal) epigenetic reader proteins, in particular BRD4 (bromodomain-containing protein 4), have emerged as potential therapeutic targets in a number of pathological conditions, including cancer and cardiovascular disease. Small-molecule BET protein inhibitors such as JQ1 have demonstrated efficacy in reversing cardiac hypertrophy and heart failure in preclinical models. Yet, genetic studies elucidating the biology of BET proteins in the heart have not been conducted to validate pharmacological findings and to unveil potential pharmacological side effects.
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