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Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma

Through the last decade, cold atmospheric plasma (CAP) has emerged as an innovative therapeutic option for cancer treatment. Recently, we have set up a potentially safe atmospheric pressure plasma jet device that displays antitumoral properties in a preclinical model of cholangiocarcinoma (CCA), a r...

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Autores principales: Vaquero, Javier, Judée, Florian, Vallette, Marie, Decauchy, Henri, Arbelaiz, Ander, Aoudjehane, Lynda, Scatton, Olivier, Gonzalez-Sanchez, Ester, Merabtene, Fatiha, Augustin, Jérémy, Housset, Chantal, Dufour, Thierry, Fouassier, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281400/
https://www.ncbi.nlm.nih.gov/pubmed/32438553
http://dx.doi.org/10.3390/cancers12051280
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author Vaquero, Javier
Judée, Florian
Vallette, Marie
Decauchy, Henri
Arbelaiz, Ander
Aoudjehane, Lynda
Scatton, Olivier
Gonzalez-Sanchez, Ester
Merabtene, Fatiha
Augustin, Jérémy
Housset, Chantal
Dufour, Thierry
Fouassier, Laura
author_facet Vaquero, Javier
Judée, Florian
Vallette, Marie
Decauchy, Henri
Arbelaiz, Ander
Aoudjehane, Lynda
Scatton, Olivier
Gonzalez-Sanchez, Ester
Merabtene, Fatiha
Augustin, Jérémy
Housset, Chantal
Dufour, Thierry
Fouassier, Laura
author_sort Vaquero, Javier
collection PubMed
description Through the last decade, cold atmospheric plasma (CAP) has emerged as an innovative therapeutic option for cancer treatment. Recently, we have set up a potentially safe atmospheric pressure plasma jet device that displays antitumoral properties in a preclinical model of cholangiocarcinoma (CCA), a rare and very aggressive cancer emerging from the biliary tree with few efficient treatments. In the present study, we aimed at deciphering the molecular mechanisms underlying the antitumor effects of CAP towards CCA in both an in vivo and in vitro context. In vivo, using subcutaneous xenografts into immunocompromised mice, CAP treatment of CCA induced DNA lesions and tumor cell apoptosis, as evaluated by 8-oxoguanine and cleaved caspase-3 immunohistochemistry, respectively. The analysis of the tumor microenvironment showed changes in markers related to macrophage polarization. In vitro, the incubation of CCA cells with CAP-treated culture media (i.e., plasma-activated media, PAM) led to a dose response decrease in cell survival. At molecular level, CAP treatment induced double-strand DNA breaks, followed by an increased phosphorylation and activation of the cell cycle master regulators CHK1 and p53, leading to cell cycle arrest and cell death by apoptosis. In conclusion, CAP is a novel therapeutic option to consider for CCA in the future.
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spelling pubmed-72814002020-06-19 Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma Vaquero, Javier Judée, Florian Vallette, Marie Decauchy, Henri Arbelaiz, Ander Aoudjehane, Lynda Scatton, Olivier Gonzalez-Sanchez, Ester Merabtene, Fatiha Augustin, Jérémy Housset, Chantal Dufour, Thierry Fouassier, Laura Cancers (Basel) Article Through the last decade, cold atmospheric plasma (CAP) has emerged as an innovative therapeutic option for cancer treatment. Recently, we have set up a potentially safe atmospheric pressure plasma jet device that displays antitumoral properties in a preclinical model of cholangiocarcinoma (CCA), a rare and very aggressive cancer emerging from the biliary tree with few efficient treatments. In the present study, we aimed at deciphering the molecular mechanisms underlying the antitumor effects of CAP towards CCA in both an in vivo and in vitro context. In vivo, using subcutaneous xenografts into immunocompromised mice, CAP treatment of CCA induced DNA lesions and tumor cell apoptosis, as evaluated by 8-oxoguanine and cleaved caspase-3 immunohistochemistry, respectively. The analysis of the tumor microenvironment showed changes in markers related to macrophage polarization. In vitro, the incubation of CCA cells with CAP-treated culture media (i.e., plasma-activated media, PAM) led to a dose response decrease in cell survival. At molecular level, CAP treatment induced double-strand DNA breaks, followed by an increased phosphorylation and activation of the cell cycle master regulators CHK1 and p53, leading to cell cycle arrest and cell death by apoptosis. In conclusion, CAP is a novel therapeutic option to consider for CCA in the future. MDPI 2020-05-19 /pmc/articles/PMC7281400/ /pubmed/32438553 http://dx.doi.org/10.3390/cancers12051280 Text en © 2020 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 Article
Vaquero, Javier
Judée, Florian
Vallette, Marie
Decauchy, Henri
Arbelaiz, Ander
Aoudjehane, Lynda
Scatton, Olivier
Gonzalez-Sanchez, Ester
Merabtene, Fatiha
Augustin, Jérémy
Housset, Chantal
Dufour, Thierry
Fouassier, Laura
Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma
title Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma
title_full Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma
title_fullStr Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma
title_full_unstemmed Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma
title_short Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma
title_sort cold-atmospheric plasma induces tumor cell death in preclinical in vivo and in vitro models of human cholangiocarcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281400/
https://www.ncbi.nlm.nih.gov/pubmed/32438553
http://dx.doi.org/10.3390/cancers12051280
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