生物
蛋白质稳态
基因组不稳定性
表观遗传学
衰老
端粒酶
机制(生物学)
早衰
生物信息学
神经科学
DNA损伤
遗传学
端粒
长寿
基因
哲学
认识论
DNA
作者
Carlos López-Otı́n,Marı́a A. Blasco,Linda Partridge,Manuel Serrano,Guido Kroemer
出处
期刊:Cell
[Elsevier]
日期:2013-06-01
卷期号:153 (6): 1194-1217
被引量:11813
标识
DOI:10.1016/j.cell.2013.05.039
摘要
Aging is characterized by a progressive loss of physiological integrity, leading to impaired function and increased vulnerability to death. This deterioration is the primary risk factor for major human pathologies, including cancer, diabetes, cardiovascular disorders, and neurodegenerative diseases. Aging research has experienced an unprecedented advance over recent years, particularly with the discovery that the rate of aging is controlled, at least to some extent, by genetic pathways and biochemical processes conserved in evolution. This Review enumerates nine tentative hallmarks that represent common denominators of aging in different organisms, with special emphasis on mammalian aging. These hallmarks are: genomic instability, telomere attrition, epigenetic alterations, loss of proteostasis, deregulated nutrient sensing, mitochondrial dysfunction, cellular senescence, stem cell exhaustion, and altered intercellular communication. A major challenge is to dissect the interconnectedness between the candidate hallmarks and their relative contributions to aging, with the final goal of identifying pharmaceutical targets to improve human health during aging, with minimal side effects.
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