Validation of the epigenetic reader bromodomain-containing protein 4 (BRD4) as a therapeutic target for treatment of airway remodeling

被引:34
|
作者
Brasier, Allan R. [1 ]
Zhou, Jia [2 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Inst Clin & Translat Res, Madison, WI 53705 USA
[2] Univ Texas Med Branch, Dept Pharmacol & Toxicol, Chem Biol Program, Galveston, TX 77555 USA
基金
美国国家卫生研究院;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; MASTER TRANSCRIPTION FACTORS; NF-KAPPA-B; PULMONARY-FIBROSIS; HISTONE ACETYLTRANSFERASE; IN-VIVO; INHIBITION; ELONGATION; PATHWAY; KINASE;
D O I
10.1016/j.drudis.2019.11.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Structural remodeling is central to the initiation and progression of many chronic lung diseases, representing an important unmet need. We examine the evidence supporting bromodomain-containing protein 4 (BRD4) as a validated biological target for treatment of airway remodeling. In epithelial cells and fibroblasts, BRD4 serves as a scaffold for chromatin remodeling complexes in active super-enhancers. In response to inflammatory stimuli, BRD4 is repositioned to innate and mesenchymal genes activating their production. Proof-of-concept studies show promising benefit of selective BRD4 inhibitors in disrupting epithelial mesenchymal transition and myofibroblast transition in diverse models of lung injury. Recent identification of biomarkers of BRD4 provides a basis for further drug development for application in viral-induced airway inflammation, COPD and interstitial lung diseases.
引用
收藏
页码:126 / 132
页数:7
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