Targeting Mitosis in Cancer: Emerging Strategies

被引:372
作者
Dominguez-Brauer, Carmen [1 ]
Thu, Kelsie L. [1 ]
Mason, Jacqueline M. [2 ]
Blaser, Heiko [1 ]
Bray, Mark R. [2 ]
Mak, Tak W. [1 ]
机构
[1] Univ Hlth Network, Ontario Canc Inst, Campbell Family Inst Breast Canc Res, Toronto, ON M5G 2M9, Canada
[2] Univ Hlth Network, Ontario Canc Inst, Campbell Family Inst Breast Canc Res, Toronto, ON M5G 1L7, Canada
基金
加拿大健康研究院;
关键词
MITOTIC SPINDLE CHECKPOINT; SMALL-MOLECULE INHIBITOR; DEPENDENT KINASE 4/6; POLO-LIKE KINASES; CELL-CYCLE; BREAST-CANCER; NEK2; KINASE; CENTROSOME DUPLICATION; EXTRA CENTROSOMES; CDK4/6; INHIBITION;
D O I
10.1016/j.molcel.2015.11.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cell cycle is an evolutionarily conserved process necessary for mammalian cell growth and development. Because cell-cycle aberrations are a hallmark of cancer, this process has been the target of anti-cancer therapeutics for decades. However, despite numerous clinical trials, cell-cycle-targeting agents have generally failed in the clinic. This review briefly examines past cell-cycle-targeted therapeutics and outlines how experience with these agents has provided valuable insight to refine and improve anti- mitotic strategies. An overview of emerging anti- mitotic approaches with promising pre-clinical results is provided, and the concept of exploiting the genomic instability of tumor cells through therapeutic inhibition of mitotic checkpoints is discussed. We believe this strategy has a high likelihood of success given its potential to enhance therapeutic index by targeting tumor-specific vulnerabilities. This reasoning stimulated our development of novel inhibitors targeting the critical regulators of genomic stability and the mitotic checkpoint: AURKA, PLK4, and Mps1/TTK.
引用
收藏
页码:524 / 536
页数:13
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