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Multiple characteristic alterations and available therapeutic strategies of cellular senescence
Given its state of stable proliferative inhibition, cellular senescence is primarily depicted as a critical mechanism by which organisms delay the progression of carcinogenesis. Cells undergoing senescence are often associated with the alteration of a series of specific features and functions, such...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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Zhejiang University Press
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936135/ https://www.ncbi.nlm.nih.gov/pubmed/36751697 http://dx.doi.org/10.1631/jzus.B2200178 |
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collection | PubMed |
description | Given its state of stable proliferative inhibition, cellular senescence is primarily depicted as a critical mechanism by which organisms delay the progression of carcinogenesis. Cells undergoing senescence are often associated with the alteration of a series of specific features and functions, such as metabolic shifts, stemness induction, and microenvironment remodeling. However, recent research has revealed more complexity associated with senescence, including adverse effects on both physiological and pathological processes. How organisms evade these harmful consequences and survive has become an urgent research issue. Several therapeutic strategies targeting senescence, including senolytics, senomorphics, immunotherapy, and function restoration, have achieved initial success in certain scenarios. In this review, we describe in detail the characteristic changes associated with cellular senescence and summarize currently available countermeasures. |
format | Online Article Text |
id | pubmed-9936135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Zhejiang University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99361352023-02-17 Multiple characteristic alterations and available therapeutic strategies of cellular senescence J Zhejiang Univ Sci B Review Given its state of stable proliferative inhibition, cellular senescence is primarily depicted as a critical mechanism by which organisms delay the progression of carcinogenesis. Cells undergoing senescence are often associated with the alteration of a series of specific features and functions, such as metabolic shifts, stemness induction, and microenvironment remodeling. However, recent research has revealed more complexity associated with senescence, including adverse effects on both physiological and pathological processes. How organisms evade these harmful consequences and survive has become an urgent research issue. Several therapeutic strategies targeting senescence, including senolytics, senomorphics, immunotherapy, and function restoration, have achieved initial success in certain scenarios. In this review, we describe in detail the characteristic changes associated with cellular senescence and summarize currently available countermeasures. Zhejiang University Press 2023-02-15 /pmc/articles/PMC9936135/ /pubmed/36751697 http://dx.doi.org/10.1631/jzus.B2200178 Text en Copyright © Zhejiang University and Springer-Verlag GmbH Germany, part of Springer Nature 2023 |
spellingShingle | Review Multiple characteristic alterations and available therapeutic strategies of cellular senescence |
title | Multiple characteristic alterations and available therapeutic strategies of cellular senescence |
title_full | Multiple characteristic alterations and available therapeutic strategies of cellular senescence |
title_fullStr | Multiple characteristic alterations and available therapeutic strategies of cellular senescence |
title_full_unstemmed | Multiple characteristic alterations and available therapeutic strategies of cellular senescence |
title_short | Multiple characteristic alterations and available therapeutic strategies of cellular senescence |
title_sort | multiple characteristic alterations and available therapeutic strategies of cellular senescence |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936135/ https://www.ncbi.nlm.nih.gov/pubmed/36751697 http://dx.doi.org/10.1631/jzus.B2200178 |
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