共 50 条
CDK4/6 Inhibition in Cancer: Beyond Cell Cycle Arrest
被引:285
|作者:
Goel, Shom
[1
,2
]
DeCristo, Molly J.
[1
]
McAllister, Sandra S.
[3
,4
,5
,6
]
Zhao, Jean J.
[1
,7
]
机构:
[1] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Med, Boston, MA USA
[4] Brigham & Womens Hosp, Dept Med, Hematol Div, Boston, MA 02115 USA
[5] Harvard Med Sch, Harvard Stem Cell Inst, Boston, MA USA
[6] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[7] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
基金:
美国国家卫生研究院;
关键词:
DEPENDENT KINASE 4/6;
BREAST-CANCER;
RETINOBLASTOMA PROTEIN;
TUBEROUS SCLEROSIS;
GENE-EXPRESSION;
CDK6;
INHIBITOR;
LUNG CANCERS;
PHASE-II;
D1;
RB;
D O I:
10.1016/j.tcb.2018.07.002
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Pharmacologic inhibitors of cyclin-dependent kinases 4 and 6 (CDK4/6) have recently entered the therapeutic armamentarium of clinical oncologists, and show promising activity in patients with breast and other cancers. Although their chief mechanism of action is inhibition of retinoblastoma (RB) protein phosphorylation and thus the induction of cell cycle arrest, CDK4/6 inhibitors alter cancer cell biology in other ways that can also be leveraged for therapeutic benefit. These include modulation of mitogenic kinase signaling, induction of a senescence-like phenotype, and enhancement of cancer cell immunogenicity. We describe here the less-appreciated effects of CDK4/6 inhibitors on cancer cells, and suggest ways by which they might be exploited to enhance the benefits of these agents for cancer patients.
引用
收藏
页码:911 / 925
页数:15
相关论文