Rzymski Tomasz, Mikula Michał, Wiklik Katarzyna, Brzózka Krzysztof
Selvita SA, Kraków, Poland.
Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland.
Biochim Biophys Acta. 2015 Oct;1854(10 Pt B):1617-29. doi: 10.1016/j.bbapap.2015.05.011. Epub 2015 May 22.
Cyclin-dependent kinase (CDK) inhibitors have been developed as potential anticancer therapeutics and several nonselective compounds are currently in advanced clinical trials. This review is focused on the key biological roles of CDK8 kinase, which provide a proof-of-principle for continued efforts toward effective cancer treatment, targeting activity of this CDK family member. Among currently identified kinase inhibitors, several displayed significant selectivity for CDK8 and notably the effectiveness in targeting cancer specific gene expression programs. Structural features of CDK8 and available ligands were discussed from a perspective of the rational drug design process. Current state of the art confirms that further development of CDK8 inhibitors will translate into targeted therapies in oncology. This article is part of a Special Issue entitled:Inhibitors of Protein Kinases.
细胞周期蛋白依赖性激酶(CDK)抑制剂已被开发为潜在的抗癌治疗药物,目前有几种非选择性化合物正处于晚期临床试验阶段。本综述聚焦于CDK8激酶的关键生物学作用,为持续致力于有效癌症治疗(靶向该CDK家族成员的活性)提供了原理证明。在目前已鉴定的激酶抑制剂中,有几种对CDK8表现出显著的选择性,尤其在靶向癌症特异性基因表达程序方面具有有效性。从合理药物设计过程的角度讨论了CDK8的结构特征和可用配体。目前的技术水平证实,CDK8抑制剂的进一步开发将转化为肿瘤学中的靶向治疗。本文是名为《蛋白激酶抑制剂》特刊的一部分。