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Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment

In this study a novel method was implemented and investigated in order to destroy cancer cells inside the mouse body on a clinical level. In the case of in-vitro study, MTT assay was employed to discover an effective dose of applied plasma and distinguish the plasma effect in direct and in indirect...

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Autores principales: Saadati, Fariba, Mahdikia, Hamed, Abbaszadeh, Hojjat-Allah, Abdollahifar, Mohammad-Amin, Khoramgah, Maryam Sadat, Shokri, Babak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955918/
https://www.ncbi.nlm.nih.gov/pubmed/29769707
http://dx.doi.org/10.1038/s41598-018-25990-9
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author Saadati, Fariba
Mahdikia, Hamed
Abbaszadeh, Hojjat-Allah
Abdollahifar, Mohammad-Amin
Khoramgah, Maryam Sadat
Shokri, Babak
author_facet Saadati, Fariba
Mahdikia, Hamed
Abbaszadeh, Hojjat-Allah
Abdollahifar, Mohammad-Amin
Khoramgah, Maryam Sadat
Shokri, Babak
author_sort Saadati, Fariba
collection PubMed
description In this study a novel method was implemented and investigated in order to destroy cancer cells inside the mouse body on a clinical level. In the case of in-vitro study, MTT assay was employed to discover an effective dose of applied plasma and distinguish the plasma effect in direct and in indirect treatments. Tumor growth was also measured in in-vivo section so that the effectiveness of direct and indirect treatments could be compared. Furthermore, an investigation was conducted to study the interferences between a conventional method (chemotherapy) and plasma treatment so as to increase the effectiveness of treatment inside the body. Hematoxylin and Eosin, Flow Cytometry, TUNEL and Western Blot assay were used to investigate any cell alteration and the impact of various treatment methods on cancer cell and amount of their apoptosis and protein levels. Radiology and CT scan images were taken to determine the final tumor volume. The results showed a significant cell death and substantial reduction in tumor growth in direct plasma treatment in comparison with indirect plasma treatment. Eventually, dramatic destruction of cancer cells was observed while using of indirect plasma-chemotherapy combination, thus introducing an effective method for deep tissue tumors can be introduced.
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spelling pubmed-59559182018-05-21 Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment Saadati, Fariba Mahdikia, Hamed Abbaszadeh, Hojjat-Allah Abdollahifar, Mohammad-Amin Khoramgah, Maryam Sadat Shokri, Babak Sci Rep Article In this study a novel method was implemented and investigated in order to destroy cancer cells inside the mouse body on a clinical level. In the case of in-vitro study, MTT assay was employed to discover an effective dose of applied plasma and distinguish the plasma effect in direct and in indirect treatments. Tumor growth was also measured in in-vivo section so that the effectiveness of direct and indirect treatments could be compared. Furthermore, an investigation was conducted to study the interferences between a conventional method (chemotherapy) and plasma treatment so as to increase the effectiveness of treatment inside the body. Hematoxylin and Eosin, Flow Cytometry, TUNEL and Western Blot assay were used to investigate any cell alteration and the impact of various treatment methods on cancer cell and amount of their apoptosis and protein levels. Radiology and CT scan images were taken to determine the final tumor volume. The results showed a significant cell death and substantial reduction in tumor growth in direct plasma treatment in comparison with indirect plasma treatment. Eventually, dramatic destruction of cancer cells was observed while using of indirect plasma-chemotherapy combination, thus introducing an effective method for deep tissue tumors can be introduced. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955918/ /pubmed/29769707 http://dx.doi.org/10.1038/s41598-018-25990-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Saadati, Fariba
Mahdikia, Hamed
Abbaszadeh, Hojjat-Allah
Abdollahifar, Mohammad-Amin
Khoramgah, Maryam Sadat
Shokri, Babak
Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment
title Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment
title_full Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment
title_fullStr Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment
title_full_unstemmed Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment
title_short Comparison of Direct and Indirect cold atmospheric-pressure plasma methods in the B(16)F(10) melanoma cancer cells treatment
title_sort comparison of direct and indirect cold atmospheric-pressure plasma methods in the b(16)f(10) melanoma cancer cells treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955918/
https://www.ncbi.nlm.nih.gov/pubmed/29769707
http://dx.doi.org/10.1038/s41598-018-25990-9
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