BRD4
溴尿嘧啶
表观遗传学
癌症研究
癌变
染色质
癌症
组蛋白
生物
肺癌
靶向治疗
医学
基因
遗传学
病理
作者
Mengmeng Zhang,Yingbo Li,Zilong Zhang,Xin Zhang,Sheng Wang,Xiaomei Song,Dongdong Zhang
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2023-10-01
卷期号:24 (14): 1079-1092
标识
DOI:10.2174/0113894501269090231012090351
摘要
Abstract: The BET protein family plays a crucial role in regulating the epigenetic landscape of the genome. Their role in regulating tumor-related gene expression and its impact on the survival of tumor cells is widely acknowledged. Among the BET family constituents, BRD4 is a significant protein. It is a bromodomain-containing protein located at the outer terminal that recognizes histones that have undergone acetylation. It is present in the promoter or enhancer region of the target gene and is responsible for initiating and sustaining the expression of genes associated with tumorigenesis. BRD4 expression is significantly elevated in various tumor types. Research has indicated that BRD4 plays a significant role in regulating various transcription factors and chromatin modification, as well as in repairing DNA damage and preserving telomere function, ultimately contributing to the survival of cancerous cells. The protein BRD4 has a significant impact on antitumor therapy, particularly in the management of lung cancer and hematological malignancies, and the promising potential of BRD4 inhibitors in the realm of cancer prevention and treatment is a topic of great interest. Therefore, BRD4 is considered a promising candidate for prophylaxis and therapy of neoplastic diseases. However, further research is required to fully comprehend the significance and indispensability of BRD4 in cancer and its potential as a therapeutic target.
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