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Connecting the Dots: From DNA Damage and Repair to Aging

Mammalian cells evolve a delicate system, the DNA damage response (DDR) pathway, to monitor genomic integrity and to prevent the damage from both endogenous end exogenous insults. Emerging evidence suggests that aberrant DDR and deficient DNA repair are strongly associated with cancer and aging. Our...

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Detalles Bibliográficos
Autores principales: Pan, Mei-Ren, Li, Kaiyi, Lin, Shiaw-Yih, Hung, Wen-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881511/
https://www.ncbi.nlm.nih.gov/pubmed/27164092
http://dx.doi.org/10.3390/ijms17050685
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author Pan, Mei-Ren
Li, Kaiyi
Lin, Shiaw-Yih
Hung, Wen-Chun
author_facet Pan, Mei-Ren
Li, Kaiyi
Lin, Shiaw-Yih
Hung, Wen-Chun
author_sort Pan, Mei-Ren
collection PubMed
description Mammalian cells evolve a delicate system, the DNA damage response (DDR) pathway, to monitor genomic integrity and to prevent the damage from both endogenous end exogenous insults. Emerging evidence suggests that aberrant DDR and deficient DNA repair are strongly associated with cancer and aging. Our understanding of the core program of DDR has made tremendous progress in the past two decades. However, the long list of the molecules involved in the DDR and DNA repair continues to grow and the roles of the new “dots” are under intensive investigation. Here, we review the connection between DDR and DNA repair and aging and discuss the potential mechanisms by which deficient DNA repair triggers systemic effects to promote physiological or pathological aging.
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spelling pubmed-48815112016-05-27 Connecting the Dots: From DNA Damage and Repair to Aging Pan, Mei-Ren Li, Kaiyi Lin, Shiaw-Yih Hung, Wen-Chun Int J Mol Sci Review Mammalian cells evolve a delicate system, the DNA damage response (DDR) pathway, to monitor genomic integrity and to prevent the damage from both endogenous end exogenous insults. Emerging evidence suggests that aberrant DDR and deficient DNA repair are strongly associated with cancer and aging. Our understanding of the core program of DDR has made tremendous progress in the past two decades. However, the long list of the molecules involved in the DDR and DNA repair continues to grow and the roles of the new “dots” are under intensive investigation. Here, we review the connection between DDR and DNA repair and aging and discuss the potential mechanisms by which deficient DNA repair triggers systemic effects to promote physiological or pathological aging. MDPI 2016-05-06 /pmc/articles/PMC4881511/ /pubmed/27164092 http://dx.doi.org/10.3390/ijms17050685 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pan, Mei-Ren
Li, Kaiyi
Lin, Shiaw-Yih
Hung, Wen-Chun
Connecting the Dots: From DNA Damage and Repair to Aging
title Connecting the Dots: From DNA Damage and Repair to Aging
title_full Connecting the Dots: From DNA Damage and Repair to Aging
title_fullStr Connecting the Dots: From DNA Damage and Repair to Aging
title_full_unstemmed Connecting the Dots: From DNA Damage and Repair to Aging
title_short Connecting the Dots: From DNA Damage and Repair to Aging
title_sort connecting the dots: from dna damage and repair to aging
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881511/
https://www.ncbi.nlm.nih.gov/pubmed/27164092
http://dx.doi.org/10.3390/ijms17050685
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