Institute for Clinical and Translational Research, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI 53705, USA.
Chemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Drug Discov Today. 2020 Jan;25(1):126-132. doi: 10.1016/j.drudis.2019.11.002. Epub 2019 Nov 13.
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.
结构重塑是许多慢性肺部疾病发生和发展的核心,代表了一个重要的未满足的需求。我们研究了支持溴结构域蛋白 4(BRD4)作为治疗气道重塑的有效生物学靶点的证据。在上皮细胞和成纤维细胞中,BRD4 作为活性超级增强子中染色质重塑复合物的支架。在炎症刺激下,BRD4 重新定位到先天和间充质基因,激活它们的产生。概念验证研究表明,选择性 BRD4 抑制剂在破坏不同肺损伤模型中的上皮间质转化和肌成纤维细胞转化方面具有良好的效果。最近对 BRD4 生物标志物的鉴定为进一步开发用于病毒诱导的气道炎症、COPD 和间质性肺病的药物提供了基础。