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Título
Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma
Autor(es)
Palabras clave
Cholangiocarcinoma
cold plasma
innovative therapy
tumor cells
macrofagos
plasma selectivity
plama jet
Clasificación UNESCO
3209 Farmacología
2403 Bioquímica
Fecha de publicación
2020
Editor
MDPI
Citación
Vaquero, 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.
Resumen
[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.
URI
DOI
10.3390/cancers12051280
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