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Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes
Radiation-induced oral mucositis is a dose-limiting toxic side effect for patients with head and neck cancer. Numerous attempts at improving radiation-induced oral mucositis have not produced a qualified treatment. Ginseng polysaccharide has multiple immunoprotective effects. Our aim was to investig...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951072/ https://www.ncbi.nlm.nih.gov/pubmed/24078877 http://dx.doi.org/10.1093/jrr/rrt109 |
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author | Chang, Jae Won Park, Keun Hyung HWANG, Hye Sook Shin, Yoo Seob Oh, Young-Taek Kim, Chul-Ho |
author_facet | Chang, Jae Won Park, Keun Hyung HWANG, Hye Sook Shin, Yoo Seob Oh, Young-Taek Kim, Chul-Ho |
author_sort | Chang, Jae Won |
collection | PubMed |
description | Radiation-induced oral mucositis is a dose-limiting toxic side effect for patients with head and neck cancer. Numerous attempts at improving radiation-induced oral mucositis have not produced a qualified treatment. Ginseng polysaccharide has multiple immunoprotective effects. Our aim was to investigate the effectiveness of Korean red ginseng (KRG) on radiation-induced damage in the human keratinocyte cell line HaCaT and in an in vivo zebrafish model. Radiation inhibited HaCaT cell proliferation and migration in a cell viability assay and wound healing assay, respectively. KRG protected against these effects. KRG attenuated the radiation-induced embryotoxicity in the zebrafish model. Irradiation of HaCaT cells caused apoptosis and changes in mitochondrial membrane potential (MMP). KRG inhibited the radiation-induced apoptosis and intracellular generation of reactive oxygen species (ROS), and stabilized the radiation-induced loss of MMP. Western blots revealed KRG-mediated reduced expression of ataxia telangiectasia mutated protein (ATM), p53, c-Jun N-terminal kinase (JNK), p38 and cleaved caspase-3, compared with their significant increase after radiation treatment. The collective results suggest that KRG protects HaCaT cells by blocking ROS generation, inhibiting changes in MMP, and inhibiting the caspase, ATM, p38 and JNK pathways. |
format | Online Article Text |
id | pubmed-3951072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39510722014-03-12 Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes Chang, Jae Won Park, Keun Hyung HWANG, Hye Sook Shin, Yoo Seob Oh, Young-Taek Kim, Chul-Ho J Radiat Res Biology Radiation-induced oral mucositis is a dose-limiting toxic side effect for patients with head and neck cancer. Numerous attempts at improving radiation-induced oral mucositis have not produced a qualified treatment. Ginseng polysaccharide has multiple immunoprotective effects. Our aim was to investigate the effectiveness of Korean red ginseng (KRG) on radiation-induced damage in the human keratinocyte cell line HaCaT and in an in vivo zebrafish model. Radiation inhibited HaCaT cell proliferation and migration in a cell viability assay and wound healing assay, respectively. KRG protected against these effects. KRG attenuated the radiation-induced embryotoxicity in the zebrafish model. Irradiation of HaCaT cells caused apoptosis and changes in mitochondrial membrane potential (MMP). KRG inhibited the radiation-induced apoptosis and intracellular generation of reactive oxygen species (ROS), and stabilized the radiation-induced loss of MMP. Western blots revealed KRG-mediated reduced expression of ataxia telangiectasia mutated protein (ATM), p53, c-Jun N-terminal kinase (JNK), p38 and cleaved caspase-3, compared with their significant increase after radiation treatment. The collective results suggest that KRG protects HaCaT cells by blocking ROS generation, inhibiting changes in MMP, and inhibiting the caspase, ATM, p38 and JNK pathways. Oxford University Press 2014-03 2013-09-26 /pmc/articles/PMC3951072/ /pubmed/24078877 http://dx.doi.org/10.1093/jrr/rrt109 Text en © The Author 2013. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biology Chang, Jae Won Park, Keun Hyung HWANG, Hye Sook Shin, Yoo Seob Oh, Young-Taek Kim, Chul-Ho Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes |
title | Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes |
title_full | Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes |
title_fullStr | Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes |
title_full_unstemmed | Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes |
title_short | Protective effects of Korean red ginseng against radiation-induced apoptosis in human HaCaT keratinocytes |
title_sort | protective effects of korean red ginseng against radiation-induced apoptosis in human hacat keratinocytes |
topic | Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951072/ https://www.ncbi.nlm.nih.gov/pubmed/24078877 http://dx.doi.org/10.1093/jrr/rrt109 |
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