Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/135204
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dc.contributor.authorEmadi, F.-
dc.contributor.authorTeo, T.-
dc.contributor.authorRahaman, M.H.-
dc.contributor.authorWang, S.-
dc.date.issued2020-
dc.identifier.citationDrug Discovery Today, 2020; 25(12):2257-2267-
dc.identifier.issn1359-6446-
dc.identifier.urihttps://hdl.handle.net/2440/135204-
dc.description.abstractCyclin-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.-
dc.description.statementofresponsibilityFatemeh Emadi, Theodosia Teo, Muhammed H. Rahaman and Shudong Wang-
dc.language.isoen-
dc.publisherElsevier-
dc.rights© 2020 Elsevier Ltd. All rights reserved.-
dc.source.urihttp://dx.doi.org/10.1016/j.drudis.2020.09.035-
dc.titleCDK12: a potential therapeutic target in cancer-
dc.typeJournal article-
dc.identifier.doi10.1016/j.drudis.2020.09.035-
pubs.publication-statusPublished-
Appears in Collections:Pharmacology publications

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