Review Volume 16, Issue 16 pp 12073—12100
Targeting multiple hallmarks of mammalian aging with combinations of interventions
- 1 Sector of Molecular Evolution, Institute for Information Transmission Problems, Russian Academy of Sciences, Moscow 127051, Russia
- 2 Open Longevity, Sherman Oaks, CA 91403, USA
- 3 Department of Molecular Biology and Genetics, Bogazici University, Istanbul 34342, Turkey
- 4 Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Pushchino 142290, Russia
- 5 Department of Surgery, Endocrine Neoplasia Laboratory, University of California, San Francisco, CA 94143, USA
Received: November 1, 2023 Accepted: June 28, 2024 Published: August 18, 2024
https://doi.org/10.18632/aging.206078How to Cite
Copyright: © 2024 Panchin et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Aging is currently viewed as a result of multiple biological processes that manifest themselves independently, reinforce each other and in their totality lead to the aged phenotype. Genetic and pharmaceutical approaches targeting specific underlying causes of aging have been used to extend the lifespan and healthspan of model organisms ranging from yeast to mammals. However, most interventions display only a modest benefit. This outcome is to be expected if we consider that even if one aging process is successfully treated, other aging pathways may remain intact. Hence solving the problem of aging may require targeting not one but many of its underlying causes at once. Here we review the challenges and successes of combination therapies aimed at increasing the lifespan of mammals and propose novel directions for their development. We conclude that both additive and synergistic effects on mammalian lifespan can be achieved by combining interventions that target the same or different hallmarks of aging. However, the number of studies in which multiple hallmarks were targeted simultaneously is surprisingly limited. We argue that this approach is as promising as it is understudied.