Epigenetic modulation by targeting bromodomain containing protein 9 (BRD9): Its therapeutic potential and selective inhibition

溴尿嘧啶 表观遗传学 染色质重塑 癌变 乙酰化 染色质 化学 生物 癌症研究 癌症 生物化学 基因 遗传学
作者
Maria Mushtaq Ali,Sehrish Naz,Sajda Ashraf,Stefan Knapp,Zaheer Ul‐Haq
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:230: 123428-123428 被引量:12
标识
DOI:10.1016/j.ijbiomac.2023.123428
摘要

The bromodomain-containing protein 9, a component of the SWI/SNF chromatin remodeling complex, functions as an 'epigenetic reader' selectively recognizing acetyl-lysine marks. It regulates chromatin structure and gene expression by recruitment of acetylated transcriptional regulators and by modulating the function of remodeling complexes. Recent data suggests that BRD9 plays an important role in regulating cellular growth and it has been suggested to drive progression of several malignant diseases such as cervical cancer, and acute myeloid leukemia. Its role in tumorigenesis suggests that selective BRD9 inhibitors may have therapeutic value in cancer therapy. Currently, there has been increasing interest in developing small molecules that can specifically target BRD9 or the closely related bromodomain protein BRD7. Available chemical probes will help to clarify biological functions of BRD9 and its potential for cancer therapy. Since the report of the first BRD9 inhibitor LP99 in 2015, numerous inhibitors have been developed. In this review, we summarized the biological roles of BRD9, structural details and the progress made in the development of BRD9 inhibitors.
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