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Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion
This study compared effects of plasma-activated medium (PAM) with effects of conventional clinical thermal therapy on both lung cancer cells and benign cells for management of malignant pleural effusion (MPE). For MPE treatment, chemotherapy, photodynamic therapy, and thermal therapy are used but ca...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584628/ https://www.ncbi.nlm.nih.gov/pubmed/33097755 http://dx.doi.org/10.1038/s41598-020-75214-2 |
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author | Cheng, Yi-Jing Lin, Ching-Kai Chen, Chao-Yu Chien, Po-Chien Chuan, Ho-Hsien Ho, Chao-Chi Cheng, Yun-Chien |
author_facet | Cheng, Yi-Jing Lin, Ching-Kai Chen, Chao-Yu Chien, Po-Chien Chuan, Ho-Hsien Ho, Chao-Chi Cheng, Yun-Chien |
author_sort | Cheng, Yi-Jing |
collection | PubMed |
description | This study compared effects of plasma-activated medium (PAM) with effects of conventional clinical thermal therapy on both lung cancer cells and benign cells for management of malignant pleural effusion (MPE). For MPE treatment, chemotherapy, photodynamic therapy, and thermal therapy are used but caused systemic side effects, patient photosensitivity, and edema, respectively. Recent studies show that plasma induces apoptosis in cancer cells with minor effects on normal cells and is cost-effective. However, the effects of plasma on MPE have not been investigated previously. This study applied a nonthermal atmospheric-pressure plasma jet to treat RPMI medium to produce PAM, carefully controlled the long-life reactive oxygen and nitrogen species concentration in PAM, and treated the cells. The influence of PAM treatment on the microenvironment of cells was also checked. The results indicated that PAM selectively inhibited CL1–5 and A549 cells, exerting minor effects on benign mesothelial and fibroblast cells. In contrast to selective lethal effects of PAM, thermal therapy inhibited both CL1–5 and benign mesothelial cells. This study also found that fibroblast growth factor 1 is not the factor explaining why PAM can selectively inhibit CL1–5 cells. These results indicate that PAM is potentially a less-harmful and cost-effective adjuvant therapy for MPE. |
format | Online Article Text |
id | pubmed-7584628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75846282020-10-27 Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion Cheng, Yi-Jing Lin, Ching-Kai Chen, Chao-Yu Chien, Po-Chien Chuan, Ho-Hsien Ho, Chao-Chi Cheng, Yun-Chien Sci Rep Article This study compared effects of plasma-activated medium (PAM) with effects of conventional clinical thermal therapy on both lung cancer cells and benign cells for management of malignant pleural effusion (MPE). For MPE treatment, chemotherapy, photodynamic therapy, and thermal therapy are used but caused systemic side effects, patient photosensitivity, and edema, respectively. Recent studies show that plasma induces apoptosis in cancer cells with minor effects on normal cells and is cost-effective. However, the effects of plasma on MPE have not been investigated previously. This study applied a nonthermal atmospheric-pressure plasma jet to treat RPMI medium to produce PAM, carefully controlled the long-life reactive oxygen and nitrogen species concentration in PAM, and treated the cells. The influence of PAM treatment on the microenvironment of cells was also checked. The results indicated that PAM selectively inhibited CL1–5 and A549 cells, exerting minor effects on benign mesothelial and fibroblast cells. In contrast to selective lethal effects of PAM, thermal therapy inhibited both CL1–5 and benign mesothelial cells. This study also found that fibroblast growth factor 1 is not the factor explaining why PAM can selectively inhibit CL1–5 cells. These results indicate that PAM is potentially a less-harmful and cost-effective adjuvant therapy for MPE. Nature Publishing Group UK 2020-10-23 /pmc/articles/PMC7584628/ /pubmed/33097755 http://dx.doi.org/10.1038/s41598-020-75214-2 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cheng, Yi-Jing Lin, Ching-Kai Chen, Chao-Yu Chien, Po-Chien Chuan, Ho-Hsien Ho, Chao-Chi Cheng, Yun-Chien Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion |
title | Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion |
title_full | Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion |
title_fullStr | Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion |
title_full_unstemmed | Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion |
title_short | Plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion |
title_sort | plasma-activated medium as adjuvant therapy for lung cancer with malignant pleural effusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584628/ https://www.ncbi.nlm.nih.gov/pubmed/33097755 http://dx.doi.org/10.1038/s41598-020-75214-2 |
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