CDK10 in Gastrointestinal Cancers: Dual Roles as a Tumor Suppressor and Oncogene

被引:14
|
作者
Bazzi, Zainab A. [1 ,2 ]
Tai, Isabella T. [1 ,2 ]
机构
[1] Univ British Columbia, Dept Med, Div Gastroenterol, Vancouver, BC, Canada
[2] British Columbia BC Canc, Canadas Michael Smith Genome Sci Ctr, Vancouver, BC, Canada
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
基金
加拿大健康研究院;
关键词
colorectal cancer; cyclin-dependent kinases; gastrointestinal cancers; hepatocellular carcinoma; gastric cancer; biliary tract cancer; CDK10; CYCLIN-DEPENDENT KINASE-5; ABERRANT DNA METHYLATION; GASTRIC-CANCER; COLORECTAL-CANCER; HEPATOCELLULAR-CARCINOMA; CELL-CYCLE; MESENCHYMAL TRANSITION; TRANSCRIPTION FACTOR; PANCREATIC-CANCER; INDUCED APOPTOSIS;
D O I
10.3389/fonc.2021.655479
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cyclin-dependent kinase 10 (CDK10) is a CDC2-related serine/threonine kinase involved in cellular processes including cell proliferation, transcription regulation and cell cycle regulation. CDK10 has been identified as both a candidate tumor suppressor in hepatocellular carcinoma, biliary tract cancers and gastric cancer, and a candidate oncogene in colorectal cancer (CRC). CDK10 has been shown to be specifically involved in modulating cancer cell proliferation, motility and chemosensitivity. Specifically, in CRC, it may represent a viable biomarker and target for chemoresistance. The development of therapeutics targeting CDK10 has been hindered by lack a specific small molecule inhibitor for CDK10 kinase activity, due to a lack of a high throughput screening assay. Recently, a novel CDK10 kinase activity assay has been developed, which will aid in the development of small molecule inhibitors targeting CDK10 activity. Discovery of a small molecular inhibitor for CDK10 would facilitate further exploration of its biological functions and affirm its candidacy as a therapeutic target, specifically for CRC.
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页数:8
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