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周期蛋白依赖性激酶 8:靶向癌症治疗的新希望?

Cyclin-Dependent Kinase 8: A New Hope in Targeted Cancer Therapy?

机构信息

Centre for Drug Discovery and Development, Sansom Institute for Health Research and School of Pharmacy and Medical Sciences , University of South Australia , Adelaide , South Australia 5001 , Australia.

出版信息

J Med Chem. 2018 Jun 28;61(12):5073-5092. doi: 10.1021/acs.jmedchem.7b00901. Epub 2018 Jan 9.

Abstract

Cyclin-dependent kinase 8 (CDK8) plays a vital role in regulating transcription either through its association with the Mediator complex or by phosphorylating transcription factors. Myriads of genetic and biochemical studies have established CDK8 as a key oncogenic driver in many cancers. Specifically, CDK8-mediated activation of oncogenic Wnt-β-catenin signaling, transcription of estrogen-inducible genes, and suppression of super enhancer-associated genes contributes to oncogenesis in colorectal, breast, and hematological malignancies, respectively. However, while most research supports the role of CDK8 as an oncogene, other work has raised the possibility of its contrary function. The diverse biological functions of CDK8 and its seemingly context-specific roles in different types of cancers have spurred a great amount of interest and perhaps an even greater amount of controversy in the development of CDK8 inhibitors as potential cancer therapeutic agents. Herein, we review the latest landscape of CDK8 biology and its involvement in carcinogenesis. We dissect current efforts in discovering CDK8 inhibitors and attempt to provide an outlook at the future of CDK8-targeted cancer therapies.

摘要

周期蛋白依赖性激酶 8(CDK8)通过与中介体复合物的结合或通过磷酸化转录因子,在调节转录中发挥重要作用。大量的遗传和生化研究已经确立 CDK8 是许多癌症中的关键致癌驱动因子。具体而言,CDK8 介导的致癌 Wnt-β-连环蛋白信号的激活、雌激素诱导基因的转录以及抑制超级增强子相关基因的表达,分别促进了结直肠癌、乳腺癌和血液系统恶性肿瘤的发生。然而,尽管大多数研究支持 CDK8 作为癌基因的作用,但其他研究提出了其相反功能的可能性。CDK8 的多种生物学功能及其在不同类型癌症中似乎特定于情境的作用,激发了人们对 CDK8 抑制剂作为潜在癌症治疗剂的极大兴趣,也许还有更多的争议。在此,我们回顾了 CDK8 生物学及其在致癌作用中的最新研究进展。我们剖析了目前发现 CDK8 抑制剂的努力,并试图对 CDK8 靶向癌症治疗的未来进行展望。

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