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Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging

Aging is a natural but relentless process of physiological decline, leading to physical frailty, reduced ability to respond to physical stresses (resilience) and, ultimately, organismal death. Cellular senescence, a self-defensive mechanism activated in response to intrinsic stimuli and/or exogenous...

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Detalles Bibliográficos
Autores principales: Sun, Yu, Li, Qingfeng, Kirkland, James L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869767/
https://www.ncbi.nlm.nih.gov/pubmed/36699942
http://dx.doi.org/10.1093/lifemedi/lnac030
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author Sun, Yu
Li, Qingfeng
Kirkland, James L
author_facet Sun, Yu
Li, Qingfeng
Kirkland, James L
author_sort Sun, Yu
collection PubMed
description Aging is a natural but relentless process of physiological decline, leading to physical frailty, reduced ability to respond to physical stresses (resilience) and, ultimately, organismal death. Cellular senescence, a self-defensive mechanism activated in response to intrinsic stimuli and/or exogenous stress, is one of the central hallmarks of aging. Senescent cells cease to proliferate, while remaining metabolically active and secreting numerous extracellular factors, a feature known as the senescence-associated secretory phenotype. Senescence is physiologically important for embryonic development, tissue repair, and wound healing, and prevents carcinogenesis. However, chronic accumulation of persisting senescent cells contributes to a host of pathologies including age-related morbidities. By paracrine and endocrine mechanisms, senescent cells can induce inflammation locally and systemically, thereby causing tissue dysfunction, and organ degeneration. Agents including those targeting damaging components of the senescence-associated secretory phenotype or inducing apoptosis of senescent cells exhibit remarkable benefits in both preclinical models and early clinical trials for geriatric conditions. Here we summarize features of senescent cells and outline strategies holding the potential to be developed as clinical interventions. In the long run, there is an increasing demand for safe, effective, and clinically translatable senotherapeutics to address healthcare needs in current settings of global aging.
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spelling pubmed-98697672023-01-23 Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging Sun, Yu Li, Qingfeng Kirkland, James L Life Med Review Aging is a natural but relentless process of physiological decline, leading to physical frailty, reduced ability to respond to physical stresses (resilience) and, ultimately, organismal death. Cellular senescence, a self-defensive mechanism activated in response to intrinsic stimuli and/or exogenous stress, is one of the central hallmarks of aging. Senescent cells cease to proliferate, while remaining metabolically active and secreting numerous extracellular factors, a feature known as the senescence-associated secretory phenotype. Senescence is physiologically important for embryonic development, tissue repair, and wound healing, and prevents carcinogenesis. However, chronic accumulation of persisting senescent cells contributes to a host of pathologies including age-related morbidities. By paracrine and endocrine mechanisms, senescent cells can induce inflammation locally and systemically, thereby causing tissue dysfunction, and organ degeneration. Agents including those targeting damaging components of the senescence-associated secretory phenotype or inducing apoptosis of senescent cells exhibit remarkable benefits in both preclinical models and early clinical trials for geriatric conditions. Here we summarize features of senescent cells and outline strategies holding the potential to be developed as clinical interventions. In the long run, there is an increasing demand for safe, effective, and clinically translatable senotherapeutics to address healthcare needs in current settings of global aging. Oxford University Press 2022-08-09 /pmc/articles/PMC9869767/ /pubmed/36699942 http://dx.doi.org/10.1093/lifemedi/lnac030 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Higher Education Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Sun, Yu
Li, Qingfeng
Kirkland, James L
Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
title Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
title_full Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
title_fullStr Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
title_full_unstemmed Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
title_short Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
title_sort targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869767/
https://www.ncbi.nlm.nih.gov/pubmed/36699942
http://dx.doi.org/10.1093/lifemedi/lnac030
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