极光抑制剂
DNA损伤
激酶
极光激酶B
支票1
极光激酶
有丝分裂
DNA修复
Polo样激酶
主轴检查点
DNA
细胞生物学
癌症研究
催化亚单位
细胞周期检查点
G2-M DNA损伤检查点
生物
遗传学
细胞周期
主轴装置
癌症
细胞分裂
蛋白激酶A
细胞
作者
Hoi Tang,Randy Y.C. Poon
出处
期刊:
日期:2020-05-01
卷期号:821: 111716-111716
被引量:105
标识
DOI:10.1016/j.mrfmmm.2020.111716
摘要
It is well established that Aurora kinases perform critical functions during mitosis. It has become increasingly clear that the Aurora kinases also perform a myriad of non-mitotic functions including DNA damage response. The available evidence indicates that inhibition Aurora kinase A (AURKA) may contribute to the G2 DNA damage checkpoint through AURKA’s functions in PLK1 and CDC25B activation. Both AURKA and Aurora kinase B (AURKB) are also essential in mitotic DNA damage response that guard against DNA damage-induced chromosome segregation errors, including the control of abscission checkpoint and prevention of micronuclei formation. Dysregulation of Aurora kinases can trigger DNA damage in mitosis that is sensed in the subsequent G1 by a p53-dependent postmitotic checkpoint. Aurora kinases are themselves linked to the G1 DNA damage checkpoint through p53 and p73 pathways. Finally, several lines of evidence provide a connection between Aurora kinases and DNA repair and apoptotic pathways. Although more studies are required to provide a comprehensive picture of how cells respond to DNA damage, these findings indicate that both AURKA and AURKB are inextricably linked to pathways guarding against DNA damage. They also provide a rationale to support more detailed studies on the synergism between small-molecule inhibitors against Aurora kinases and DNA-damaging agents in cancer therapies.
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