The Science of Aging and Longevity

Sara Sunil Mohite, Shahbaz Akhtar Momin, Samip Anant Niwate, Riya Madanlal Paliwal, Khushboo Chhotelal Yadav, S. Shukla, Dileep Kumar Bharati
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Abstract

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 contribution to aging, with the final goal of identifying pharmaceutical targets to improve human health during aging with minimal side-effects.
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衰老与长寿的科学
衰老的特征是生理完整性的逐渐丧失,导致功能受损和对死亡的脆弱性增加。这种退化是主要人类疾病的主要危险因素,包括癌症、糖尿病、心血管疾病和神经退行性疾病。近年来,衰老研究取得了前所未有的进展,特别是发现衰老的速度至少在一定程度上是由进化中保守的遗传途径和生化过程控制的。这篇综述列举了代表不同生物体衰老的共同特征的九个暂定标志,特别强调哺乳动物的衰老。这些特征是:基因组不稳定、端粒磨损、表观遗传改变、蛋白质平衡丧失、营养感知失调、线粒体功能障碍、细胞衰老、干细胞衰竭和细胞间通讯改变。一个主要的挑战是解剖候选标志及其对衰老的相对贡献之间的相互联系,最终目标是确定药物靶点,以最小的副作用改善衰老过程中的人类健康。
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