Restoring order at the cell cycle border: Co-targeting CDK4/6 and CDK2

被引:9
|
作者
Jeselsohn, Rinath [1 ,2 ,3 ]
Schiff, Rachel [4 ,5 ]
Grinshpun, Albert [1 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Breast Oncol Ctr, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Div Mol & Cellular Oncol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Ctr Funct Canc Epigenet, Boston, MA 02115 USA
[4] Baylor Coll Med, Dept Med, Lester & Sue Smith Breast Ctr, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Mol & Cellular Biol, Lester & Sue Smith Breast Ctr, Houston, TX 77030 USA
关键词
D O I
10.1016/j.ccell.2021.08.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Overcoming resistance to CDK4/6 inhibitors is a major clinical challenge. In this issue of Cancer Cell, Freeman-Cook et al. study mechanisms of resistance to CDK4/6 inhibitors by employing a CRISPRa screen. They identify the cyclin E-CDK2 axis and Myc signaling as key pathways of resistance and develop PF-06873600, a selective CDK2/4/6 inhibitor.
引用
收藏
页码:1302 / 1305
页数:5
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