DNA损伤
DNA修复
氧化应激
细胞生物学
生物
DNA
基因组不稳定性
支票1
氧化磷酸化
细胞周期检查点
细胞周期
遗传学
细胞凋亡
生物化学
作者
Yan Shen Shan,Melanie Sorrell,Zachary Berman
标识
DOI:10.1007/s00018-014-1666-4
摘要
To maintain genome stability, cells have evolved various DNA repair pathways to deal with oxidative DNA damage. DNA damage response (DDR) pathways, including ATM-Chk2 and ATR-Chk1 checkpoints, are also activated in oxidative stress to coordinate DNA repair, cell cycle progression, transcription, apoptosis, and senescence. Several studies demonstrate that DDR pathways can regulate DNA repair pathways. On the other hand, accumulating evidence suggests that DNA repair pathways may modulate DDR pathway activation as well. In this review, we summarize our current understanding of how various DNA repair and DDR pathways are activated in response to oxidative DNA damage primarily from studies in eukaryotes. In particular, we analyze the functional interplay between DNA repair and DDR pathways in oxidative stress. A better understanding of cellular response to oxidative stress may provide novel avenues of treating human diseases, such as cancer and neurodegenerative disorders.
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