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Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells
OBJECTIVE: Myricetin, a common dietary flavonoid is widely distributed in fruits and vegetables, and is used as a health food supplement based on its immune function, anti-oxidation, anti-tumor, and anti-inflammatory properties. The aim of this study was to investigate the effects of myricetin on co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994494/ https://www.ncbi.nlm.nih.gov/pubmed/24650056 http://dx.doi.org/10.1186/1746-1596-9-68 |
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author | Zhang, Shijie Wang, Lei Liu, Hongchun Zhao, Guoqiang Ming, Liang |
author_facet | Zhang, Shijie Wang, Lei Liu, Hongchun Zhao, Guoqiang Ming, Liang |
author_sort | Zhang, Shijie |
collection | PubMed |
description | OBJECTIVE: Myricetin, a common dietary flavonoid is widely distributed in fruits and vegetables, and is used as a health food supplement based on its immune function, anti-oxidation, anti-tumor, and anti-inflammatory properties. The aim of this study was to investigate the effects of myricetin on combination with radiotherapy enhance radiosensitivity of lung cancer A549 and H1299 cells. METHODS: A549 cells and H1299 cells were exposed to X-ray with or without myricetin treatment. Colony formation assays, CCK-8 assay, flow cytometry and Caspase-3 level detection were used to evaluate the radiosensitization activity of myricetin on cell proliferation and apoptosis in vitro. Nude mouse tumor xenograft model was built to assessed radiosensitization effect of myricetin in vivo. RESULTS: Compared with the exposed group without myricetin treatment, the groups treated with myricetin showed significantly suppressed cell surviving fraction and proliferation, increased the cell apoptosis and increased Caspase-3 protein expression after X-ray exposure in vitro. And in vivo assay, growth speed of tumor xenografts was significantly decreased in irradiated mice treated with myricetin. CONCLUSIONS: The study demonstrated both in vitro and in vivo evidence that combination of myricetin with radiotherapy can enhance tumor radiosensitivity of pulmonary carcinoma A549 and H1299 cells, and myricetin could be a potential radiosensitizer for lung cancer therapy. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5791518001210633 |
format | Online Article Text |
id | pubmed-3994494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39944942014-04-23 Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells Zhang, Shijie Wang, Lei Liu, Hongchun Zhao, Guoqiang Ming, Liang Diagn Pathol Research OBJECTIVE: Myricetin, a common dietary flavonoid is widely distributed in fruits and vegetables, and is used as a health food supplement based on its immune function, anti-oxidation, anti-tumor, and anti-inflammatory properties. The aim of this study was to investigate the effects of myricetin on combination with radiotherapy enhance radiosensitivity of lung cancer A549 and H1299 cells. METHODS: A549 cells and H1299 cells were exposed to X-ray with or without myricetin treatment. Colony formation assays, CCK-8 assay, flow cytometry and Caspase-3 level detection were used to evaluate the radiosensitization activity of myricetin on cell proliferation and apoptosis in vitro. Nude mouse tumor xenograft model was built to assessed radiosensitization effect of myricetin in vivo. RESULTS: Compared with the exposed group without myricetin treatment, the groups treated with myricetin showed significantly suppressed cell surviving fraction and proliferation, increased the cell apoptosis and increased Caspase-3 protein expression after X-ray exposure in vitro. And in vivo assay, growth speed of tumor xenografts was significantly decreased in irradiated mice treated with myricetin. CONCLUSIONS: The study demonstrated both in vitro and in vivo evidence that combination of myricetin with radiotherapy can enhance tumor radiosensitivity of pulmonary carcinoma A549 and H1299 cells, and myricetin could be a potential radiosensitizer for lung cancer therapy. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5791518001210633 BioMed Central 2014-03-20 /pmc/articles/PMC3994494/ /pubmed/24650056 http://dx.doi.org/10.1186/1746-1596-9-68 Text en Copyright © 2014 Zhang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhang, Shijie Wang, Lei Liu, Hongchun Zhao, Guoqiang Ming, Liang Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells |
title | Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells |
title_full | Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells |
title_fullStr | Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells |
title_full_unstemmed | Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells |
title_short | Enhancement of recombinant myricetin on the radiosensitivity of lung cancer A549 and H1299 cells |
title_sort | enhancement of recombinant myricetin on the radiosensitivity of lung cancer a549 and h1299 cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994494/ https://www.ncbi.nlm.nih.gov/pubmed/24650056 http://dx.doi.org/10.1186/1746-1596-9-68 |
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