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From cellular senescence to age-associated diseases: the miRNA connection

Cellular senescence has evolved from an in-vitro model system to study aging in vitro to a multifaceted phenomenon of in-vivo importance as senescent cells in vivo have been identified and their removal delays the onset of age-associated diseases in a mouse model system. From the large emerging clas...

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Detalles Bibliográficos
Autores principales: Schraml, Elisabeth, Grillari, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922944/
https://www.ncbi.nlm.nih.gov/pubmed/24472232
http://dx.doi.org/10.1186/2046-2395-1-10
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author Schraml, Elisabeth
Grillari, Johannes
author_facet Schraml, Elisabeth
Grillari, Johannes
author_sort Schraml, Elisabeth
collection PubMed
description Cellular senescence has evolved from an in-vitro model system to study aging in vitro to a multifaceted phenomenon of in-vivo importance as senescent cells in vivo have been identified and their removal delays the onset of age-associated diseases in a mouse model system. From the large emerging class of non-coding RNAs, miRNAs have only recently been functionally implied in the regulatory networks that are modified during the aging process. Here we summarize examples of similarities between the differential expression of miRNAs during senescence and age-associated diseases and suggest that these similarities might emphasize the importance of senescence for the pathogenesis of age-associated diseases. Understanding such a connection on the level of miRNAs might offer valuable opportunities for designing novel diagnostic and therapeutic strategies.
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spelling pubmed-39229442014-02-14 From cellular senescence to age-associated diseases: the miRNA connection Schraml, Elisabeth Grillari, Johannes Longev Healthspan Review Cellular senescence has evolved from an in-vitro model system to study aging in vitro to a multifaceted phenomenon of in-vivo importance as senescent cells in vivo have been identified and their removal delays the onset of age-associated diseases in a mouse model system. From the large emerging class of non-coding RNAs, miRNAs have only recently been functionally implied in the regulatory networks that are modified during the aging process. Here we summarize examples of similarities between the differential expression of miRNAs during senescence and age-associated diseases and suggest that these similarities might emphasize the importance of senescence for the pathogenesis of age-associated diseases. Understanding such a connection on the level of miRNAs might offer valuable opportunities for designing novel diagnostic and therapeutic strategies. BioMed Central 2012-12-03 /pmc/articles/PMC3922944/ /pubmed/24472232 http://dx.doi.org/10.1186/2046-2395-1-10 Text en Copyright © 2012 Schraml and Grillari; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Schraml, Elisabeth
Grillari, Johannes
From cellular senescence to age-associated diseases: the miRNA connection
title From cellular senescence to age-associated diseases: the miRNA connection
title_full From cellular senescence to age-associated diseases: the miRNA connection
title_fullStr From cellular senescence to age-associated diseases: the miRNA connection
title_full_unstemmed From cellular senescence to age-associated diseases: the miRNA connection
title_short From cellular senescence to age-associated diseases: the miRNA connection
title_sort from cellular senescence to age-associated diseases: the mirna connection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922944/
https://www.ncbi.nlm.nih.gov/pubmed/24472232
http://dx.doi.org/10.1186/2046-2395-1-10
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