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Molecular damage in aging

2021; Nature Portfolio; Volume: 1; Issue: 12 Linguagem: Inglês

10.1038/s43587-021-00150-3

2662-8465

Vadim N. Gladyshev, Stephen B. Kritchevsky, Steven Clarke, Ana María Cuervo, Oliver Fiehn, João Pedro de Magalhães, Theresa Mau, Michal Maes, Robert L. Moritz, Laura J. Niedernhofer, Emile Van Schaftingen, Gregory J. Tranah, Kenneth Walsh, Yoshimitsu Yura, Bohan Zhang, Steven R. Cummings,

Mitochondrial Function and Pathology

Cellular metabolism and environmental interactions generate molecular damage affecting all levels of biological organization. Accumulation of this damage over time is thought to have a central role in the aging process. Insufficient attention has been paid to the role of molecular damage in aging-related phenotypes, particularly in humans, in part because of the difficulty in measuring its various forms. Recently, omics approaches have been developed that begin to address this challenge, because they can assess a sizable proportion of age-related damage at the level of small molecules, proteins, RNA, DNA, organelles and cells. This Review describes the concept of molecular damage in aging and discusses its diverse aspects from theoretical models to experimental approaches. Measurement of multiple types of damage enables studies of the role of damage in aging and lays a foundation for testing interventions that reduce the burden of molecular damage, thereby targeting aging. In this Review, the authors discuss the concept of molecular damage in aging, from theoretical models to experimental approaches and how to test interventions targeting aging that reduce its burden.