CDK inhibitors in cancer therapy: what is next?

The pursuit for drugs that inhibit cyclin-dependent kinases (CDKs) has been an intense area of research for more than 15 years. The first-generation inhibitors, Flavopiridol and CY-202, are in late-stage clinical trials, but so far have demonstrated only modest activity. Several second-generation in...

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Veröffentlicht in:Trends in pharmacological sciences (Regular ed.) 2008-01, Vol.29 (1), p.16-21
Hauptverfasser: Malumbres, Marcos, Pevarello, Paolo, Barbacid, Mariano, Bischoff, James R
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container_title Trends in pharmacological sciences (Regular ed.)
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creator Malumbres, Marcos
Pevarello, Paolo
Barbacid, Mariano
Bischoff, James R
description The pursuit for drugs that inhibit cyclin-dependent kinases (CDKs) has been an intense area of research for more than 15 years. The first-generation inhibitors, Flavopiridol and CY-202, are in late-stage clinical trials, but so far have demonstrated only modest activity. Several second-generation inhibitors are now in clinical trials. Future approaches to determine clinical benefit need to incorporate both the lessons learned from these early compounds and information recently obtained from the genetic analysis of CDKs in preclinical models. Here we discuss key concepts that should be considered when validating the clinical utility of CDK inhibitors in cancer therapy.
doi_str_mv 10.1016/j.tips.2007.10.012
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subjects Advanced Basic Science
Animals
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Cell Cycle - drug effects
Clinical Trials as Topic
Cyclin-Dependent Kinases - antagonists & inhibitors
Drug Delivery Systems
Enzyme Inhibitors - pharmacology
Enzyme Inhibitors - therapeutic use
Humans
Neoplasms - drug therapy
title CDK inhibitors in cancer therapy: what is next?
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