CDK8 as a therapeutic target for cancers and recent developments in discovery of CDK8 inhibitors

被引:45
|
作者
Xi, Meiyang [1 ]
Chen, Tingkai [2 ]
Wu, Chunlei [1 ]
Gao, Xiaozhong [1 ]
Wu, Yonghua [1 ]
Luo, Xiang [1 ]
Du, Kui [1 ]
Yu, Lemao [1 ]
Cai, Tao [1 ]
Shen, Runpu [1 ]
Sun, Haopeng [2 ]
机构
[1] Shaoxing Univ, Coll Chem & Chem Engn, Shaoxing 312000, Peoples R China
[2] China Pharmaceut Univ, Dept Med Chem, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Cancer; Overexpression; CDK8; inhibitors; Selectivity; DEPENDENT KINASE 8; E2F1 TRANSCRIPTIONAL ACTIVITY; BETA-CATENIN; COLORECTAL-CANCER; MEDIATOR COMPLEX; SMALL-MOLECULE; CELL-CYCLE; POSITIVE REGULATOR; POTENT; CORTISTATIN;
D O I
10.1016/j.ejmech.2018.11.076
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cyclin-dependent kinases 8 (CDK8) regulates transcriptional process via associating with the mediator complex or phosphorylating transcription factors (TF). Overexpression of CDK8 has been observed in various cancers. It mediates aberrant activation of Wnt/beta-catenin signaling pathway, which is initially recognized and best studied in colorectal cancer (CRC). CDK8 acts as an oncogene and represents a potential target for developing novel CDK8 inhibitors in cancer therapeutics. However, other study has revealed its contrary role. The function of CDK8 is context dependent. Even so, a variety of potent and selective CDK8 inhibitors have been discovered after crystal structures were resolved in two states (active or inactive). In this review, we summarize co-crystal structures, biological mechanisms, dysregulation in cancers and recent progress in the field of CDK8 inhibitors, trying to offer an outlook of CDK8 inhibitors in cancer therapy in future. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:77 / 91
页数:15
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