| Literature DB >> 29731395 |
Mary E Klein1, Marta Kovatcheva1, Lara E Davis2, William D Tap3, Andrew Koff4.
Abstract
CDK4/6 inhibitors are among a new generation of therapeutics. Building upon the striking success of the combination of CDK4/6 inhibitors and the hormone receptor antagonist letrozole in breast cancer, many other combinations have recently entered clinical trials in multiple diseases. To achieve maximal benefit with CDK4/6 inhibitors it will be critical to understand the cellular mechanisms by which they act. Here we highlight the mechanisms by which CDK4/6 inhibitors can exert their anti-tumor activities beyond simply enforcing cytostatic growth arrest, and discuss how this knowledge may inform new combinations, improve outcomes, and modify dosing schedules in the future.Entities:
Keywords: CDK4/6 inhibitors; abemaciclib; metabolism; palbociclib; ribociclib; senescence; tumor microenvironment
Mesh:
Substances:
Year: 2018 PMID: 29731395 PMCID: PMC6039233 DOI: 10.1016/j.ccell.2018.03.023
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743