Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest

Many environmental and physiological stresses are chronic. Thus, cells are constantly exposed to diverse types of genotoxic insults that challenge genome stability, including those that induce oxidative DNA damage. However, most in vitro studies that model cellular response to oxidative stressors em...

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Fecha de publicación:
2016
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/27532
Acceso en línea:
https://doi.org/10.1016/j.redox.2016.07.004
https://repository.urosario.edu.co/handle/10336/27532
Palabra clave:
ROS
Genotoxicity
DNA damage response
Up-regulation of DNA repair genes
G2/M arrest
Adaptation
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dc.title.spa.fl_str_mv Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
dc.title.TranslatedTitle.spa.fl_str_mv Respuesta adaptativa distintiva a la exposición repetida al peróxido de hidrógeno asociada con la regulación positiva de los genes de reparación del ADN y la detención del ciclo celular
title Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
spellingShingle Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
ROS
Genotoxicity
DNA damage response
Up-regulation of DNA repair genes
G2/M arrest
Adaptation
title_short Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
title_full Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
title_fullStr Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
title_full_unstemmed Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
title_sort Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
dc.subject.keyword.spa.fl_str_mv ROS
Genotoxicity
DNA damage response
Up-regulation of DNA repair genes
G2/M arrest
Adaptation
topic ROS
Genotoxicity
DNA damage response
Up-regulation of DNA repair genes
G2/M arrest
Adaptation
description Many environmental and physiological stresses are chronic. Thus, cells are constantly exposed to diverse types of genotoxic insults that challenge genome stability, including those that induce oxidative DNA damage. However, most in vitro studies that model cellular response to oxidative stressors employ short exposures and/or acute stress models. In this study, we tested the hypothesis that chronic and repeated exposure to a micromolar concentration of hydrogen peroxide (H2O2) could activate DNA damage responses, resulting in cellular adaptations. For this purpose, we developed an in vitro model in which we incubated mouse myoblast cells with a steady concentration of ~50 ?M H2O2 for one hour daily for seven days, followed by a final challenge of a 10 or 20X higher dose of H2O2 (0.5 or 1 mM). We report that intermittent long-term exposure to this oxidative stimulus nearly eliminated cell toxicity and significantly decreased genotoxicity (in particular, a >5-fold decreased in double-strand breaks) resulting from subsequent acute exposure to oxidative stress. This protection was associated with cell cycle arrest in G2/M and induction of expression of nine DNA repair genes. Together, this evidence supports an adaptive response to chronic, low-level oxidative stress that results in genomic protection and up-regulated maintenance of cellular homeostasis.
publishDate 2016
dc.date.created.spa.fl_str_mv 2016-10
dc.date.accessioned.none.fl_str_mv 2020-08-19T14:42:36Z
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dc.type.eng.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.redox.2016.07.004
dc.identifier.issn.none.fl_str_mv ISSN: 2213-2317
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/27532
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https://repository.urosario.edu.co/handle/10336/27532
identifier_str_mv ISSN: 2213-2317
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 133
dc.relation.citationStartPage.none.fl_str_mv 124
dc.relation.citationTitle.none.fl_str_mv Redox Biology
dc.relation.citationVolume.none.fl_str_mv Vol. 9
dc.relation.ispartof.spa.fl_str_mv Redox Biology, ISSN: 2213-2317, Vol.9 (2016); pp. 124-133
dc.relation.uri.spa.fl_str_mv https://www.sciencedirect.com/science/article/pii/S2213231716300751?via%3Dihub
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dc.publisher.spa.fl_str_mv Elsevier
dc.source.spa.fl_str_mv Redox Biology
institution Universidad del Rosario
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dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
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