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Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study

Malignant melanoma is considered to be a heterogeneous disease that arises from altered genes and transformed melanocytes. In this study, special softjet cold atmospheric plasma was used to treat three different human melanoma cells using air and N(2) gases to check the anti-melanoma activity. The p...

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Autores principales: Yadav, Dharmendra Kumar, Adhikari, Manish, Kumar, Surendra, Ghimire, Bhagirath, Han, Ihn, Kim, Mi-Hyun, Choi, Eun-Ha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042335/
https://www.ncbi.nlm.nih.gov/pubmed/32099012
http://dx.doi.org/10.1038/s41598-020-60356-0
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author Yadav, Dharmendra Kumar
Adhikari, Manish
Kumar, Surendra
Ghimire, Bhagirath
Han, Ihn
Kim, Mi-Hyun
Choi, Eun-Ha
author_facet Yadav, Dharmendra Kumar
Adhikari, Manish
Kumar, Surendra
Ghimire, Bhagirath
Han, Ihn
Kim, Mi-Hyun
Choi, Eun-Ha
author_sort Yadav, Dharmendra Kumar
collection PubMed
description Malignant melanoma is considered to be a heterogeneous disease that arises from altered genes and transformed melanocytes. In this study, special softjet cold atmospheric plasma was used to treat three different human melanoma cells using air and N(2) gases to check the anti-melanoma activity. The physical effects by plasma revealed an increase in the temperature with the gradual reduction in pH at 60 sec, 180 sec and 300 sec air and N(2) plasma treatment. Cellular toxicity revealed a decreased in cell survival (~50% cell survival using air gas and <~60% cell survival using N(2) gas at 60 sec plasma treatment in G-361 cells). Gene analysis by q-PCR revealed that 3 min and 5 min air and N(2) plasma treatment activated apoptotic pathways by triggering apoptotic genes in all three melanoma cell lines. The apoptosis was confirmed by DAPI staining and its related pathways were further explored according to protein-protein docking, and their probable activation mechanism was revealed. The pathways highlighted that activation of apoptosis which leads to cellular cascades and hence stimulation ASK1 (docking method) revealed that softjet plasma can be an effective modality for human melanoma treatment.
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spelling pubmed-70423352020-03-03 Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study Yadav, Dharmendra Kumar Adhikari, Manish Kumar, Surendra Ghimire, Bhagirath Han, Ihn Kim, Mi-Hyun Choi, Eun-Ha Sci Rep Article Malignant melanoma is considered to be a heterogeneous disease that arises from altered genes and transformed melanocytes. In this study, special softjet cold atmospheric plasma was used to treat three different human melanoma cells using air and N(2) gases to check the anti-melanoma activity. The physical effects by plasma revealed an increase in the temperature with the gradual reduction in pH at 60 sec, 180 sec and 300 sec air and N(2) plasma treatment. Cellular toxicity revealed a decreased in cell survival (~50% cell survival using air gas and <~60% cell survival using N(2) gas at 60 sec plasma treatment in G-361 cells). Gene analysis by q-PCR revealed that 3 min and 5 min air and N(2) plasma treatment activated apoptotic pathways by triggering apoptotic genes in all three melanoma cell lines. The apoptosis was confirmed by DAPI staining and its related pathways were further explored according to protein-protein docking, and their probable activation mechanism was revealed. The pathways highlighted that activation of apoptosis which leads to cellular cascades and hence stimulation ASK1 (docking method) revealed that softjet plasma can be an effective modality for human melanoma treatment. Nature Publishing Group UK 2020-02-25 /pmc/articles/PMC7042335/ /pubmed/32099012 http://dx.doi.org/10.1038/s41598-020-60356-0 Text en © The Author(s) 2020 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
Yadav, Dharmendra Kumar
Adhikari, Manish
Kumar, Surendra
Ghimire, Bhagirath
Han, Ihn
Kim, Mi-Hyun
Choi, Eun-Ha
Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study
title Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study
title_full Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study
title_fullStr Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study
title_full_unstemmed Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study
title_short Cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study
title_sort cold atmospheric plasma generated reactive species aided inhibitory effects on human melanoma cells: an in vitro and in silico study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042335/
https://www.ncbi.nlm.nih.gov/pubmed/32099012
http://dx.doi.org/10.1038/s41598-020-60356-0
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