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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:
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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