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Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner
Oral cancer accounts for ~2% of all cancers worldwide, and therapeutic intervention is closely associated with quality of life. Here, we evaluated the effects of non-thermal plasma on oral squamous cell carcinoma cells with special reference to catalytic Fe(II). Non-thermal plasma exerted a specific...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667380/ https://www.ncbi.nlm.nih.gov/pubmed/31379408 http://dx.doi.org/10.3164/jcbn.18-91 |
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author | Sato, Kotaro Shi, Lei Ito, Fumiya Ohara, Yuuki Motooka, Yashiro Tanaka, Hiromasa Mizuno, Masaaki Hori, Masaru Hirayama, Tasuku Hibi, Hideharu Toyokuni, Shinya |
author_facet | Sato, Kotaro Shi, Lei Ito, Fumiya Ohara, Yuuki Motooka, Yashiro Tanaka, Hiromasa Mizuno, Masaaki Hori, Masaru Hirayama, Tasuku Hibi, Hideharu Toyokuni, Shinya |
author_sort | Sato, Kotaro |
collection | PubMed |
description | Oral cancer accounts for ~2% of all cancers worldwide, and therapeutic intervention is closely associated with quality of life. Here, we evaluated the effects of non-thermal plasma on oral squamous cell carcinoma cells with special reference to catalytic Fe(II). Non-thermal plasma exerted a specific killing effect on oral squamous cell carcinoma cells in comparison to fibroblasts. Furthermore, the effect was dependent on the amounts of catalytic Fe(II), present especially in lysosomes. After non-thermal plasma application, lipid peroxidation occurred and peroxides and mitochondrial superoxide were generated. Cancer cell death by non-thermal plasma was promoted dose-dependently by prior application of ferric ammonium citrate and prevented by desferrioxamine, suggesting the association of ferroptosis. Potential involvement of apoptosis was also observed with positive terminal deoxynucleaotidyl transferase-mediated dUTP nick end labeling and annexin V results. Non-thermal plasma exposure significantly suppressed the migratory, invasive and colony-forming abilities of squamous cell carcinoma cells. The oral cavity is easily observable; therefore, non-thermal plasma can be directly applied to the oral cavity to kill oral squamous cell carcinoma without damaging fibroblasts. In conclusion, non-thermal plasma treatment is a potential therapeutic option for oral cancer. |
format | Online Article Text |
id | pubmed-6667380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-66673802019-08-02 Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner Sato, Kotaro Shi, Lei Ito, Fumiya Ohara, Yuuki Motooka, Yashiro Tanaka, Hiromasa Mizuno, Masaaki Hori, Masaru Hirayama, Tasuku Hibi, Hideharu Toyokuni, Shinya J Clin Biochem Nutr Original Article Oral cancer accounts for ~2% of all cancers worldwide, and therapeutic intervention is closely associated with quality of life. Here, we evaluated the effects of non-thermal plasma on oral squamous cell carcinoma cells with special reference to catalytic Fe(II). Non-thermal plasma exerted a specific killing effect on oral squamous cell carcinoma cells in comparison to fibroblasts. Furthermore, the effect was dependent on the amounts of catalytic Fe(II), present especially in lysosomes. After non-thermal plasma application, lipid peroxidation occurred and peroxides and mitochondrial superoxide were generated. Cancer cell death by non-thermal plasma was promoted dose-dependently by prior application of ferric ammonium citrate and prevented by desferrioxamine, suggesting the association of ferroptosis. Potential involvement of apoptosis was also observed with positive terminal deoxynucleaotidyl transferase-mediated dUTP nick end labeling and annexin V results. Non-thermal plasma exposure significantly suppressed the migratory, invasive and colony-forming abilities of squamous cell carcinoma cells. The oral cavity is easily observable; therefore, non-thermal plasma can be directly applied to the oral cavity to kill oral squamous cell carcinoma without damaging fibroblasts. In conclusion, non-thermal plasma treatment is a potential therapeutic option for oral cancer. the Society for Free Radical Research Japan 2019-07 2019-06-01 /pmc/articles/PMC6667380/ /pubmed/31379408 http://dx.doi.org/10.3164/jcbn.18-91 Text en Copyright © 2019 JCBN http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sato, Kotaro Shi, Lei Ito, Fumiya Ohara, Yuuki Motooka, Yashiro Tanaka, Hiromasa Mizuno, Masaaki Hori, Masaru Hirayama, Tasuku Hibi, Hideharu Toyokuni, Shinya Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner |
title | Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner |
title_full | Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner |
title_fullStr | Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner |
title_full_unstemmed | Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner |
title_short | Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner |
title_sort | non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic fe(ii)-dependent manner |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667380/ https://www.ncbi.nlm.nih.gov/pubmed/31379408 http://dx.doi.org/10.3164/jcbn.18-91 |
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