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Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines
The aim of this study was to investigate the effect and the mechanism of gamma linolenic acid (GLA) treatment on human hepatocellular (HCC) cell lines. The human HCC cell line HuH7 was exposed to GLA. Cell proliferation and reactive oxygen species (ROS) generation including lipid peroxidation and ap...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901768/ https://www.ncbi.nlm.nih.gov/pubmed/20664735 http://dx.doi.org/10.3164/jcbn.10-24 |
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author | Itoh, Shinji Taketomi, Akinobu Harimoto, Norifumi Tsujita, Eiji Rikimaru, Tatsuya Shirabe, Ken Shimada, Mitsuo Maehara, Yoshihiko |
author_facet | Itoh, Shinji Taketomi, Akinobu Harimoto, Norifumi Tsujita, Eiji Rikimaru, Tatsuya Shirabe, Ken Shimada, Mitsuo Maehara, Yoshihiko |
author_sort | Itoh, Shinji |
collection | PubMed |
description | The aim of this study was to investigate the effect and the mechanism of gamma linolenic acid (GLA) treatment on human hepatocellular (HCC) cell lines. The human HCC cell line HuH7 was exposed to GLA. Cell proliferation and reactive oxygen species (ROS) generation including lipid peroxidation and apoptosis were compared. We then used a cDNA microarray analysis to investigate the molecular changes induced by GLA. GLA treatment significantly reduced cell proliferation, generated ROS, and induced apoptosis. After 24 h exposure of Huh7 cells to GLA, we identified several genes encoding the antioxidant proteins to be upregulated: heme oxygenase-1 (HO-1), aldo-keto reductase 1 family C1 (AKR1C1), C4 (AKR1C4), and thioredoxin (Trx). The HO-1 protein levels were overexpressed in Huh7 cells after GLA exposure using a Western blot analysis. Furthermore, chromium mesoporphyrin (CrMP), an inhibitor of HO activity, significantly potentiated GLA cytotoxicity. GLA treatment has induced cell growth inhibition, ROS generation including lipid peroxidation, and HO-1 production for antioxidant protection against oxidative stress caused by GLA in Huh7 cells. GLA treatment should be considered as a therapeutic modality in patients with advanced HCC. |
format | Text |
id | pubmed-2901768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-29017682010-07-27 Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines Itoh, Shinji Taketomi, Akinobu Harimoto, Norifumi Tsujita, Eiji Rikimaru, Tatsuya Shirabe, Ken Shimada, Mitsuo Maehara, Yoshihiko J Clin Biochem Nutr Original Article The aim of this study was to investigate the effect and the mechanism of gamma linolenic acid (GLA) treatment on human hepatocellular (HCC) cell lines. The human HCC cell line HuH7 was exposed to GLA. Cell proliferation and reactive oxygen species (ROS) generation including lipid peroxidation and apoptosis were compared. We then used a cDNA microarray analysis to investigate the molecular changes induced by GLA. GLA treatment significantly reduced cell proliferation, generated ROS, and induced apoptosis. After 24 h exposure of Huh7 cells to GLA, we identified several genes encoding the antioxidant proteins to be upregulated: heme oxygenase-1 (HO-1), aldo-keto reductase 1 family C1 (AKR1C1), C4 (AKR1C4), and thioredoxin (Trx). The HO-1 protein levels were overexpressed in Huh7 cells after GLA exposure using a Western blot analysis. Furthermore, chromium mesoporphyrin (CrMP), an inhibitor of HO activity, significantly potentiated GLA cytotoxicity. GLA treatment has induced cell growth inhibition, ROS generation including lipid peroxidation, and HO-1 production for antioxidant protection against oxidative stress caused by GLA in Huh7 cells. GLA treatment should be considered as a therapeutic modality in patients with advanced HCC. the Society for Free Radical Research Japan 2010-07 2010-06-22 /pmc/articles/PMC2901768/ /pubmed/20664735 http://dx.doi.org/10.3164/jcbn.10-24 Text en Copyright © 2010 JCBN 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 Itoh, Shinji Taketomi, Akinobu Harimoto, Norifumi Tsujita, Eiji Rikimaru, Tatsuya Shirabe, Ken Shimada, Mitsuo Maehara, Yoshihiko Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines |
title | Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines |
title_full | Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines |
title_fullStr | Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines |
title_full_unstemmed | Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines |
title_short | Antineoplastic Effects of Gamma Linolenic Acid on Hepatocellular Carcinoma Cell Lines |
title_sort | antineoplastic effects of gamma linolenic acid on hepatocellular carcinoma cell lines |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901768/ https://www.ncbi.nlm.nih.gov/pubmed/20664735 http://dx.doi.org/10.3164/jcbn.10-24 |
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