Cyclin-Dependent Kinase 4 and 6 Inhibitors as Breast Cancer Therapy: Research Progress and Prospects

被引:1
|
作者
Li, Xiandeng [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Coll Pharm, Chengdu 611137, Peoples R China
关键词
CDK4; 6; inhibitors; metastatic breast cancer; HR plus; Her2-; palbociclib; ribociclib; abemaciclib; CDK4/6; INHIBITION; SELECTIVE INHIBITOR; ANTITUMOR-ACTIVITY; PD; 0332991; PHASE-I; D1; PROLIFERATION; ABEMACICLIB; EXPRESSION; CELLS;
D O I
10.1007/s11094-022-02599-x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cyclin-dependent kinases 4 and 6 (CDK4/6) are the core part of the cell cycle control machinery, which bind to cyclin D to regulate cell G1-S cycle conversion. CDK4/6 inhibitors are currently used to treat HR-positive and HER2-negative (HR+/HER2-) metastatic breast cancer (MBC), and the US FDA has approved three CDK4/6 inhibitors as palbociclib, ribociclib and abemaciclib. In order to provide better reference for the development of CDK4/6 inhibitors, this review summarized the research progress of CDK4/6 inhibitors. Potential drug resistance mechanism and combining medication strategies have been reviewed to reduce the occurrence of drug resistance. CDK4/6 inhibitors combined with fulvestrant or anastrozole showed positive efficacy in the treatment of breast cancer. Reducing the side effects is the crux of the development of CDK4/6 inhibitors in the future.
引用
收藏
页码:71 / 77
页数:7
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