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Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines

Compelling evidence suggests that Cold Atmospheric Pressure Plasma (CAPP) has potential as a new cancer therapy. However, knowledge about cellular signaling events and toxicity subsequent to plasma treatment is still poorly documented. The aim of this study was to focus on the interaction between 3...

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Autores principales: Dezest, Marlène, Chavatte, Laurent, Bourdens, Marion, Quinton, Damien, Camus, Mylène, Garrigues, Luc, Descargues, Pascal, Arbault, Stéphane, Burlet-Schiltz, Odile, Casteilla, Louis, Clément, Franck, Planat, Valérie, Bulteau, Anne-Laure
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264585/
https://www.ncbi.nlm.nih.gov/pubmed/28120925
http://dx.doi.org/10.1038/srep41163
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author Dezest, Marlène
Chavatte, Laurent
Bourdens, Marion
Quinton, Damien
Camus, Mylène
Garrigues, Luc
Descargues, Pascal
Arbault, Stéphane
Burlet-Schiltz, Odile
Casteilla, Louis
Clément, Franck
Planat, Valérie
Bulteau, Anne-Laure
author_facet Dezest, Marlène
Chavatte, Laurent
Bourdens, Marion
Quinton, Damien
Camus, Mylène
Garrigues, Luc
Descargues, Pascal
Arbault, Stéphane
Burlet-Schiltz, Odile
Casteilla, Louis
Clément, Franck
Planat, Valérie
Bulteau, Anne-Laure
author_sort Dezest, Marlène
collection PubMed
description Compelling evidence suggests that Cold Atmospheric Pressure Plasma (CAPP) has potential as a new cancer therapy. However, knowledge about cellular signaling events and toxicity subsequent to plasma treatment is still poorly documented. The aim of this study was to focus on the interaction between 3 different types of plasma (He, He-O(2), He-N(2)) and human epithelial cell lines to gain better insight into plasma-cell interaction. We provide evidence that reactive oxygen and nitrogen species (RONS) are inducing cell death by apoptosis and that the proteasome, a major intracellular proteolytic system which is important for tumor cell growth and survival, is a target of (He or He-N(2)) CAPP. However, RONS are not the only actors involved in cell death; electric field and charged particles could play a significant role especially for He-O(2) CAPP. By differential label-free quantitative proteomic analysis we found that CAPP triggers antioxidant and cellular defense but is also affecting extracellular matrix in keratinocytes. Moreover, we found that malignant cells are more resistant to CAPP treatment than normal cells. Taken together, our findings provide insight into potential mechanisms of CAPP-induced proteasome inactivation and the cellular consequences of these events.
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spelling pubmed-52645852017-01-30 Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines Dezest, Marlène Chavatte, Laurent Bourdens, Marion Quinton, Damien Camus, Mylène Garrigues, Luc Descargues, Pascal Arbault, Stéphane Burlet-Schiltz, Odile Casteilla, Louis Clément, Franck Planat, Valérie Bulteau, Anne-Laure Sci Rep Article Compelling evidence suggests that Cold Atmospheric Pressure Plasma (CAPP) has potential as a new cancer therapy. However, knowledge about cellular signaling events and toxicity subsequent to plasma treatment is still poorly documented. The aim of this study was to focus on the interaction between 3 different types of plasma (He, He-O(2), He-N(2)) and human epithelial cell lines to gain better insight into plasma-cell interaction. We provide evidence that reactive oxygen and nitrogen species (RONS) are inducing cell death by apoptosis and that the proteasome, a major intracellular proteolytic system which is important for tumor cell growth and survival, is a target of (He or He-N(2)) CAPP. However, RONS are not the only actors involved in cell death; electric field and charged particles could play a significant role especially for He-O(2) CAPP. By differential label-free quantitative proteomic analysis we found that CAPP triggers antioxidant and cellular defense but is also affecting extracellular matrix in keratinocytes. Moreover, we found that malignant cells are more resistant to CAPP treatment than normal cells. Taken together, our findings provide insight into potential mechanisms of CAPP-induced proteasome inactivation and the cellular consequences of these events. Nature Publishing Group 2017-01-25 /pmc/articles/PMC5264585/ /pubmed/28120925 http://dx.doi.org/10.1038/srep41163 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Dezest, Marlène
Chavatte, Laurent
Bourdens, Marion
Quinton, Damien
Camus, Mylène
Garrigues, Luc
Descargues, Pascal
Arbault, Stéphane
Burlet-Schiltz, Odile
Casteilla, Louis
Clément, Franck
Planat, Valérie
Bulteau, Anne-Laure
Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines
title Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines
title_full Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines
title_fullStr Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines
title_full_unstemmed Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines
title_short Mechanistic insights into the impact of Cold Atmospheric Pressure Plasma on human epithelial cell lines
title_sort mechanistic insights into the impact of cold atmospheric pressure plasma on human epithelial cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264585/
https://www.ncbi.nlm.nih.gov/pubmed/28120925
http://dx.doi.org/10.1038/srep41163
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