Molecular Medicine Research Center, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Curr Drug Targets. 2019;20(4):453-464. doi: 10.2174/1389450119666181026152221.
Cyclin Dependent Kinase 9 (CDK9) as a serine/threonine kinase belongs to a great number of CDKs. CDK9 is the main core of PTEF-b complex and phosphorylates RNA polymerase (RNAP) II besides other transcription factors which regulate gene transcription elongation in numerous physiological processes. Multi-functional nature of CDK9 in diverse cellular pathways proposes that it is as an appealing target. In this review, we summarized the recent findings on the molecular interaction of CDK9 with critical participant molecules to modulate their activity in various diseases. Furthermore, the presented review provides a rationale supporting the use of CDK9 as a therapeutic target in clinical developments for crucial diseases; particularly cancers will be reviewed.
周期蛋白依赖性激酶 9(CDK9)作为丝氨酸/苏氨酸激酶,属于大量 CDKs 之一。CDK9 是 PTEF-b 复合物的主要核心,除了其他转录因子之外,它还磷酸化 RNA 聚合酶(RNAP)II,从而调节许多生理过程中的基因转录延伸。CDK9 在多种细胞途径中的多功能性质表明它是一个有吸引力的靶点。在这篇综述中,我们总结了 CDK9 与关键参与分子的分子相互作用的最新发现,以调节它们在各种疾病中的活性。此外,本综述提供了支持将 CDK9 用作关键疾病(特别是癌症)临床开发中治疗靶点的依据。