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• W1943260956 endingPage "852" @default.
• W1943260956 startingPage "846" @default.
• W1943260956 abstract "Cyclin-dependent kinases (CDKs) have been considered promising drug targets for a number of years, but most CDK inhibitors have failed rigorous clinical testing. Recent studies demonstrating clear anticancer efficacy and reduced toxicity of CDK4/6 inhibitors such as palbociclib and multi-CDK inhibitors such as dinaciclib have rejuvenated the field. Favorable results with palbociclib and its recent U.S. Food and Drug Administration approval demonstrate that CDK inhibitors with narrow selectivity profiles can have clinical utility for therapy based on individual tumor genetics. A brief overview of results obtained with ATP-competitive inhibitors such as palbociclib and dinaciclib is presented, followed by a compilation of new avenues that have been pursued toward the development of novel, non-ATP-competitive CDK inhibitors. These creative ways to develop CDK inhibitors are presented along with crystal structures of these agents complexed with CDK2 to highlight differences in their binding sites and mechanisms of action. The recent successes of CDK inhibitors in the clinic, combined with the potential for structure-based routes to the development of non-ATP-competitive CDK inhibitors, and evidence that CDK inhibitors may have use in suppressing chromosomal instability and in synthetic lethal drug combinations inspire optimism that CDK inhibitors will become important weapons in the fight against cancer." @default.
• W1943260956 created "2016-06-24" @default.
• W1943260956 creator A5014140014 @default.
• W1943260956 creator A5021962959 @default.
• W1943260956 creator A5037060910 @default.
• W1943260956 creator A5051568194 @default.
• W1943260956 date "2015-05-27" @default.
• W1943260956 modified "2023-10-16" @default.
• W1943260956 title "Cyclin-Dependent Kinase Inhibitors as Anticancer Therapeutics" @default.
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