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dc.contributor.authorVaquero, Javier
dc.contributor.authorJudée, Florian
dc.contributor.authorVallette, Marie
dc.contributor.authorDecauchy, Henri
dc.contributor.authorArbelaiz, Ander
dc.contributor.authorAoudjehane, Lynda
dc.contributor.authorScatton, Olivier
dc.contributor.authorGonzález Sánchez, María Ester 
dc.contributor.authorMerabtene, Fatiha
dc.contributor.authorAugustin, Jérémy
dc.contributor.authorHousset, Chantal
dc.contributor.authorDufour, Thierry
dc.contributor.authorFouassier, Laura
dc.date.accessioned2026-02-09T10:26:59Z
dc.date.available2026-02-09T10:26:59Z
dc.date.issued2020
dc.identifier.citationVaquero, J., Judée, F., Vallette, M., Decauchy, H., Arbelaiz, A., Aoudjehane, L., Scatton, O., Gonzalez-Sanchez, E., Merabtene, F., Augustin, J., Housset, C, Dufour, T., Fouassier, L. (2020). Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma. Cancers: 12: 1280.es_ES
dc.identifier.urihttp://hdl.handle.net/10366/169638
dc.description.abstract[EN]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.es_ES
dc.description.sponsorshipJ.V. and F.J. are recipient of the LABEX PLAS@PAR (ANR-11-IDEX-0004-02). This work was funded by the LABEX Plas@par project, and received financial state aid managed by the Agence Nationale de la Recherche, as part of the programme “Investissements d’avenir” (ANR-11-IDEX-0004-02), the program Emergence@ Sorbonne Université 2016, the French Ministry of Solidarity and Health and Inserm, INCA-DGOS-Inserm_12560),the « Région Ile-de-France » (Sesame, Ref. 16016309) and the Platform program of Sorbonne Université. T.D. andL.F. are supported by “le programme Emergence 2019 Cancéropôle Ile de France” (Projet ASCLEPIOS 193602) et“le programmeAmorçage 2019 SiRIC Curamus” (Projet PROMISE 195741). L.F. is supported by Agence Nationale dela Recherche (ANR-17-CE14-0013-01) and A.A. by Fondation pour la Recherche Médicale (FRM SPF201809007054).es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAttribution 3.0 Unported*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/*
dc.subjectCholangiocarcinomaes_ES
dc.subjectcold plasmaes_ES
dc.subjectinnovative therapyes_ES
dc.subjecttumor cellses_ES
dc.subjectmacrofagoses_ES
dc.subjectplasma selectivityes_ES
dc.subjectplama jetes_ES
dc.subject.meshMacrophages *
dc.subject.meshCholangiocarcinoma *
dc.subject.meshTumor Cells, Cultured *
dc.titleCold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinomaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.3390/cancers12051280es_ES
dc.subject.unesco3209 Farmacologíaes_ES
dc.subject.unesco2403 Bioquímicaes_ES
dc.identifier.doi10.3390/cancers12051280
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid32438553
dc.identifier.essn2072-6694
dc.journal.titleCancerses_ES
dc.volume.number12es_ES
dc.issue.number5es_ES
dc.page.initial1280es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsmacrófagos *
dc.subject.decscélulas tumorales cultivadas *
dc.subject.decscolangiocarcinoma *


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Attribution 3.0 Unported
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