Sonawane Yogesh A, Taylor Margaret A, Napoleon John Victor, Rana Sandeep, Contreras Jacob I, Natarajan Amarnath
Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center , Omaha, Nebraska 68198-6805, United States.
J Med Chem. 2016 Oct 13;59(19):8667-8684. doi: 10.1021/acs.jmedchem.6b00150. Epub 2016 Jun 3.
Cyclin dependent kinase (CDK) inhibitors have been the topic of intense research for nearly 2 decades due to their widely varied and critical functions within the cell. Recently CDK9 has emerged as a druggable target for the development of cancer therapeutics. CDK9 plays a crucial role in transcription regulation; specifically, CDK9 mediated transcriptional regulation of short-lived antiapoptotic proteins is critical for the survival of transformed cells. Focused chemical libraries based on a plethora of scaffolds have resulted in mixed success with regard to the development of selective CDK9 inhibitors. Here we review the regulation of CDK9, its cellular functions, and common core structures used to target CDK9, along with their selectivity profile and efficacy in vitro and in vivo.
细胞周期蛋白依赖性激酶(CDK)抑制剂在近20年一直是深入研究的主题,因为它们在细胞内具有广泛多样且至关重要的功能。最近,CDK9已成为癌症治疗药物开发的一个可成药靶点。CDK9在转录调控中起着关键作用;具体而言,CDK9介导的短命抗凋亡蛋白的转录调控对于转化细胞的存活至关重要。基于大量支架的聚焦化学文库在选择性CDK9抑制剂的开发方面取得了喜忧参半的成果。在这里,我们综述了CDK9的调控、其细胞功能、用于靶向CDK9的常见核心结构,以及它们的选择性概况和体外及体内疗效。