Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/135204
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Type: Journal article
Title: CDK12: a potential therapeutic target in cancer
Author: Emadi, F.
Teo, T.
Rahaman, M.H.
Wang, S.
Citation: Drug Discovery Today, 2020; 25(12):2257-2267
Publisher: Elsevier
Issue Date: 2020
ISSN: 1359-6446
Statement of
Responsibility: 
Fatemeh Emadi, Theodosia Teo, Muhammed H. Rahaman and Shudong Wang
Abstract: Cyclin-dependent kinase (CDK) 12 engages in diversified biological functions, from transcription, post-transcriptional modification, cell cycle, and translation to cellular proliferation. Moreover, it regulates the expression of cancer-related genes involved in DNA damage response (DDR) and replication, which are responsible for maintaining genomic stability. CDK12 emerges as an oncogene or tumor suppressor in different cellular contexts, where its dysregulation results in tumorigenesis. Current CDK12 inhibitors are nonselective, which impedes the process of pharmacological target validation and drug development. Herein, we discuss the latest understanding of the biological roles of CDK12 in cancers and provide molecular analyses of CDK12 inhibitors to guide the rational design of selective inhibitors.
Rights: © 2020 Elsevier Ltd. All rights reserved.
DOI: 10.1016/j.drudis.2020.09.035
Published version: http://dx.doi.org/10.1016/j.drudis.2020.09.035
Appears in Collections:Pharmacology publications

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