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Context-dependent effects of cellular senescence in cancer development

Cellular senescence is an established tumour-suppressive mechanism that prevents the proliferation of premalignant cells. However, several lines of evidence show that senescent cells, which often persist in vivo, can also promote tumour progression in addition to other age-related pathologies via th...

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Autores principales: Lecot, Pacome, Alimirah, Fatouma, Desprez, Pierre-Yves, Campisi, Judith, Wiley, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891501/
https://www.ncbi.nlm.nih.gov/pubmed/27140310
http://dx.doi.org/10.1038/bjc.2016.115
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author Lecot, Pacome
Alimirah, Fatouma
Desprez, Pierre-Yves
Campisi, Judith
Wiley, Christopher
author_facet Lecot, Pacome
Alimirah, Fatouma
Desprez, Pierre-Yves
Campisi, Judith
Wiley, Christopher
author_sort Lecot, Pacome
collection PubMed
description Cellular senescence is an established tumour-suppressive mechanism that prevents the proliferation of premalignant cells. However, several lines of evidence show that senescent cells, which often persist in vivo, can also promote tumour progression in addition to other age-related pathologies via the senescence-associated secretory phenotype (SASP). Moreover, new insights suggest the SASP can facilitate tissue repair. Here, we review the beneficial and detrimental roles of senescent cells, highlighting conditions under which the senescence response does and does not promote pathology, particularly cancer. By better understanding the context-dependent effects of cellular senescence, it may be feasible to limit its detrimental properties while preserving its beneficial effects, and develop novel therapeutic strategies to prevent or treat cancer and possibly other age-associated diseases.
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spelling pubmed-48915012016-06-10 Context-dependent effects of cellular senescence in cancer development Lecot, Pacome Alimirah, Fatouma Desprez, Pierre-Yves Campisi, Judith Wiley, Christopher Br J Cancer Minireview Cellular senescence is an established tumour-suppressive mechanism that prevents the proliferation of premalignant cells. However, several lines of evidence show that senescent cells, which often persist in vivo, can also promote tumour progression in addition to other age-related pathologies via the senescence-associated secretory phenotype (SASP). Moreover, new insights suggest the SASP can facilitate tissue repair. Here, we review the beneficial and detrimental roles of senescent cells, highlighting conditions under which the senescence response does and does not promote pathology, particularly cancer. By better understanding the context-dependent effects of cellular senescence, it may be feasible to limit its detrimental properties while preserving its beneficial effects, and develop novel therapeutic strategies to prevent or treat cancer and possibly other age-associated diseases. Nature Publishing Group 2016-05-24 2016-05-03 /pmc/articles/PMC4891501/ /pubmed/27140310 http://dx.doi.org/10.1038/bjc.2016.115 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Minireview
Lecot, Pacome
Alimirah, Fatouma
Desprez, Pierre-Yves
Campisi, Judith
Wiley, Christopher
Context-dependent effects of cellular senescence in cancer development
title Context-dependent effects of cellular senescence in cancer development
title_full Context-dependent effects of cellular senescence in cancer development
title_fullStr Context-dependent effects of cellular senescence in cancer development
title_full_unstemmed Context-dependent effects of cellular senescence in cancer development
title_short Context-dependent effects of cellular senescence in cancer development
title_sort context-dependent effects of cellular senescence in cancer development
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891501/
https://www.ncbi.nlm.nih.gov/pubmed/27140310
http://dx.doi.org/10.1038/bjc.2016.115
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