A Senescence-Centric View of Aging Implications for Longevity and Disease

被引:146
|
作者
Borghesan, M. [1 ]
Hoogaars, W. M. H. [1 ]
Varela-Eirin, M. [1 ]
Talma, N. [1 ]
Demaria, M. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen UMCG, European Res Inst Biol Ageing ERIBA, Antonius Deusinglaan 1, NL-9715 RA Groningen, Netherlands
关键词
INHIBITING OXIDATIVE STRESS; CELLULAR SENESCENCE; INDUCED OSTEOPOROSIS; SATELLITE CELLS; MOUSE MODEL; STEM-CELLS; CANCER; OSTEOARTHRITIS; ATHEROSCLEROSIS; PROGRESSION;
D O I
10.1016/j.tcb.2020.07.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cellular senescence is a state of stable cell cycle arrest associated with macromolecular alterations and secretion of proinfiammatory cytokines and molecules. From their initial discovery in the 1960s, senescent cells have been hypothesized as potential contributors to the age-associated loss of regenerative potential. Here, we discuss recent evidence that implicates cellular senescence as a central regulatory mechanism of the aging process. We provide a comprehensive overview of age-associated pathologies in which cellular senescence has been implicated. We describe mechanisms by which senescent cells drive aging and diseases, and we discuss updates on exploiting these mechanisms as therapeutic targets. Finally, we critically analyze the use of senotherapeutics and their translation to the clinic, highlighting limitations and suggesting ideas for future applications and developments.
引用
收藏
页码:777 / 791
页数:15
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