端粒
衰老
生物
DNA损伤
细胞生物学
谢尔特林
端粒酶
表型
细胞衰老
细胞周期
细胞周期检查点
DNA修复
DNA
基因组不稳定性
遗传学
细胞
基因
DNA结合蛋白
转录因子
作者
Philip M. Reaper,Fabrizio d’Adda di Fagagna,Stephen P. Jackson
出处
期刊:Cell Cycle
[Taylor & Francis]
日期:2004-05-01
卷期号:3 (5): 541-544
被引量:60
摘要
Critical telomere shortening induces senescence in many normal human cell types grown in culture. Recent data have revealed that dysfunctional telomeres can resemble certain forms of DNA damage, and point to a role for DNA damage signaling in the establishment and maintenance of telomere-initiated senescence. Here, we review these new observations and highlight potential avenues of future research. We consider the identities of the key DNA damage response factors involved in senescence and discuss a model for the molecular events occurring in pre-senescent cells that ultimately lead to a permanent cell cycle arrest phenotype.
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