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The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma
Hydrogen peroxide (H(2)O(2)) is an important signaling molecule in cancer cells. However, the significant secretion of H(2)O(2) by cancer cells have been rarely observed. Cold atmospheric plasma (CAP) is a near room temperature ionized gas composed of neutral particles, charged particles, reactive s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589829/ https://www.ncbi.nlm.nih.gov/pubmed/28883477 http://dx.doi.org/10.1038/s41598-017-11480-x |
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author | Yan, Dayun Cui, Haitao Zhu, Wei Talbot, Annie Zhang, Lijie Grace Sherman, Jonathan H. Keidar, Michael |
author_facet | Yan, Dayun Cui, Haitao Zhu, Wei Talbot, Annie Zhang, Lijie Grace Sherman, Jonathan H. Keidar, Michael |
author_sort | Yan, Dayun |
collection | PubMed |
description | Hydrogen peroxide (H(2)O(2)) is an important signaling molecule in cancer cells. However, the significant secretion of H(2)O(2) by cancer cells have been rarely observed. Cold atmospheric plasma (CAP) is a near room temperature ionized gas composed of neutral particles, charged particles, reactive species, and electrons. Here, we first demonstrated that breast cancer cells and pancreatic adenocarcinoma cells generated micromolar level H(2)O(2) during just 1 min of direct CAP treatment on these cells. The cell-based H(2)O(2) generation is affected by the medium volume, the cell confluence, as well as the discharge voltage. The application of cold atmospheric plasma (CAP) in cancer treatment has been intensively investigated over the past decade. Several cellular responses to CAP treatment have been observed including the consumption of the CAP-originated reactive species, the rise of intracellular reactive oxygen species, the damage on DNA and mitochondria, as well as the activation of apoptotic events. This is a new previously unknown cellular response to CAP, which provides a new prospective to understand the interaction between CAP and cells in vitro and in vivo. The short-lived reactive species in CAP may activate cells in vivo to generate long-lived reactive species such as H(2)O(2), which may trigger immune attack on tumorous tissues via the H(2)O(2)-mediated lymphocyte activation. |
format | Online Article Text |
id | pubmed-5589829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55898292017-09-13 The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma Yan, Dayun Cui, Haitao Zhu, Wei Talbot, Annie Zhang, Lijie Grace Sherman, Jonathan H. Keidar, Michael Sci Rep Article Hydrogen peroxide (H(2)O(2)) is an important signaling molecule in cancer cells. However, the significant secretion of H(2)O(2) by cancer cells have been rarely observed. Cold atmospheric plasma (CAP) is a near room temperature ionized gas composed of neutral particles, charged particles, reactive species, and electrons. Here, we first demonstrated that breast cancer cells and pancreatic adenocarcinoma cells generated micromolar level H(2)O(2) during just 1 min of direct CAP treatment on these cells. The cell-based H(2)O(2) generation is affected by the medium volume, the cell confluence, as well as the discharge voltage. The application of cold atmospheric plasma (CAP) in cancer treatment has been intensively investigated over the past decade. Several cellular responses to CAP treatment have been observed including the consumption of the CAP-originated reactive species, the rise of intracellular reactive oxygen species, the damage on DNA and mitochondria, as well as the activation of apoptotic events. This is a new previously unknown cellular response to CAP, which provides a new prospective to understand the interaction between CAP and cells in vitro and in vivo. The short-lived reactive species in CAP may activate cells in vivo to generate long-lived reactive species such as H(2)O(2), which may trigger immune attack on tumorous tissues via the H(2)O(2)-mediated lymphocyte activation. Nature Publishing Group UK 2017-09-07 /pmc/articles/PMC5589829/ /pubmed/28883477 http://dx.doi.org/10.1038/s41598-017-11480-x Text en © The Author(s) 2017 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 Yan, Dayun Cui, Haitao Zhu, Wei Talbot, Annie Zhang, Lijie Grace Sherman, Jonathan H. Keidar, Michael The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma |
title | The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma |
title_full | The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma |
title_fullStr | The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma |
title_full_unstemmed | The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma |
title_short | The Strong Cell-based Hydrogen Peroxide Generation Triggered by Cold Atmospheric Plasma |
title_sort | strong cell-based hydrogen peroxide generation triggered by cold atmospheric plasma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589829/ https://www.ncbi.nlm.nih.gov/pubmed/28883477 http://dx.doi.org/10.1038/s41598-017-11480-x |
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