Cellular senescence in age-related disorders.


Journal

Translational research : the journal of laboratory and clinical medicine
ISSN: 1878-1810
Titre abrégé: Transl Res
Pays: United States
ID NLM: 101280339

Informations de publication

Date de publication:
12 2020
Historique:
received: 17 12 2019
revised: 15 06 2020
accepted: 16 06 2020
pubmed: 23 6 2020
medline: 9 2 2021
entrez: 23 6 2020
Statut: ppublish

Résumé

Much of the population is now faced with an enormous burden of age-associated chronic diseases. Recent discoveries in geroscience indicate that healthspan in model organisms such as mice can be manipulated by targeting cellular senescence, a hallmark mechanism of aging, defined as an irreversible proliferative arrest that occurs when cells experience oncogenic or other diverse forms of damage. Senescent cells and their proinflammatory secretome have emerged as contributors to age-related tissue dysfunction and morbidity. Cellular senescence has causal roles in mediating osteoporosis, frailty, cardiovascular diseases, osteoarthritis, pulmonary fibrosis, renal diseases, neurodegenerative diseases, hepatic steatosis, and metabolic dysfunction. Therapeutically targeting senescent cells in mice can prevent, delay, or alleviate each of these conditions. Therefore, senotherapeutic approaches, including senolytics and senomorphics, that either selectively eliminate senescent cells or interfere with their ability to promote tissue dysfunction, are gaining momentum as potential realistic strategies to abrogate human senescence to thereby compress morbidity and extend healthspan.

Identifiants

pubmed: 32569840
pii: S1931-5244(20)30146-8
doi: 10.1016/j.trsl.2020.06.007
pmc: PMC7572662
mid: NIHMS1605554
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

96-104

Subventions

Organisme : NIAMS NIH HHS
ID : K01 AR070241
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG062413
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK128552
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG065868
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

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Auteurs

Japneet Kaur (J)

Division of Endocrinology, Mayo Clinic College of Medicine, Mayo Clinic, Rochester Minnesota; Robert and Arlene Kogod Center on Aging, Mayo Clinic College of Medicine, Mayo Clinic, Rochester Minnesota.

Joshua N Farr (JN)

Division of Endocrinology, Mayo Clinic College of Medicine, Mayo Clinic, Rochester Minnesota; Robert and Arlene Kogod Center on Aging, Mayo Clinic College of Medicine, Mayo Clinic, Rochester Minnesota; Division of Physiology and Biomedical Engineering; Mayo Clinic College of Medicine, Mayo Clinic, Rochester, Minnesota. Electronic address: farr.joshua@mayo.edu.

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