Highlights of the Latest Advances in Research on CDK Inhibitors

Jonas Cicenas(SIB Swiss Institute of Bioinformatics), K. Pavan Kalyan(Haffkine Institute), Aleksandras Sorokinas, Asta Jatulyte, D. Valiūnas(Nature Research Centre), Algirdas Kaupinis(Vilnius University), Mindaugas Valius(Vilnius University)
Cancers
October 27, 2014
Cited by 128Open Access
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Abstract

Uncontrolled proliferation is the hallmark of cancer and other proliferative disorders and abnormal cell cycle regulation is, therefore, common in these diseases. Cyclin-dependent kinases (CDKs) play a crucial role in the control of the cell cycle and proliferation. These kinases are frequently deregulated in various cancers, viral infections, neurodegenerative diseases, ischemia and some proliferative disorders. This led to a rigorous pursuit for small-molecule CDK inhibitors for therapeutic uses. Early efforts to block CDKs with nonselective CDK inhibitors led to little specificity and efficacy but apparent toxicity, but the recent advance of selective CDK inhibitors allowed the first successful efforts to target these kinases for the therapies of several diseases. Major ongoing efforts are to develop CDK inhibitors as monotherapies and rational combinations with chemotherapy and other targeted drugs.


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