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Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells

BACKGROUND: It is widely recognized that astaxanthin (ASX), a member of the carotenoid family, has strong biological activities including antioxidant, anti-inflammation, and immune-modulation activities. Previous studies have confirmed that ASX can effectively inhibit hepatoma cells in vitro. MATERI...

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Autores principales: Shao, Yiye, Ni, Yanbo, Yang, Jing, Lin, Xutao, Li, Jun, Zhang, Lixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922829/
https://www.ncbi.nlm.nih.gov/pubmed/27333866
http://dx.doi.org/10.12659/MSM.899419
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author Shao, Yiye
Ni, Yanbo
Yang, Jing
Lin, Xutao
Li, Jun
Zhang, Lixia
author_facet Shao, Yiye
Ni, Yanbo
Yang, Jing
Lin, Xutao
Li, Jun
Zhang, Lixia
author_sort Shao, Yiye
collection PubMed
description BACKGROUND: It is widely recognized that astaxanthin (ASX), a member of the carotenoid family, has strong biological activities including antioxidant, anti-inflammation, and immune-modulation activities. Previous studies have confirmed that ASX can effectively inhibit hepatoma cells in vitro. MATERIAL/METHODS: MTT was used to assay proliferation of mice H22 cells, and flow cytometry was used to determine apoptosis and cell cycle arrest of H22 cells in vitro and in vivo. Moreover, anti-tumor activity of ASX was observed in mice. RESULTS: ASX inhibited the proliferation of H22 cells, promoted cell necrosis, and induced cell cycle arrest in G2 phase in vitro and in vivo. CONCLUSIONS: This study indicated that ASX can inhibit proliferation and induce apoptosis and cell cycle arrest in mice H22 hepatoma cells in vitro and in vivo.
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spelling pubmed-49228292016-07-11 Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells Shao, Yiye Ni, Yanbo Yang, Jing Lin, Xutao Li, Jun Zhang, Lixia Med Sci Monit Animal Study BACKGROUND: It is widely recognized that astaxanthin (ASX), a member of the carotenoid family, has strong biological activities including antioxidant, anti-inflammation, and immune-modulation activities. Previous studies have confirmed that ASX can effectively inhibit hepatoma cells in vitro. MATERIAL/METHODS: MTT was used to assay proliferation of mice H22 cells, and flow cytometry was used to determine apoptosis and cell cycle arrest of H22 cells in vitro and in vivo. Moreover, anti-tumor activity of ASX was observed in mice. RESULTS: ASX inhibited the proliferation of H22 cells, promoted cell necrosis, and induced cell cycle arrest in G2 phase in vitro and in vivo. CONCLUSIONS: This study indicated that ASX can inhibit proliferation and induce apoptosis and cell cycle arrest in mice H22 hepatoma cells in vitro and in vivo. International Scientific Literature, Inc. 2016-06-23 /pmc/articles/PMC4922829/ /pubmed/27333866 http://dx.doi.org/10.12659/MSM.899419 Text en © Med Sci Monit, 2016 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
spellingShingle Animal Study
Shao, Yiye
Ni, Yanbo
Yang, Jing
Lin, Xutao
Li, Jun
Zhang, Lixia
Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells
title Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells
title_full Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells
title_fullStr Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells
title_full_unstemmed Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells
title_short Astaxanthin Inhibits Proliferation and Induces Apoptosis and Cell Cycle Arrest of Mice H22 Hepatoma Cells
title_sort astaxanthin inhibits proliferation and induces apoptosis and cell cycle arrest of mice h22 hepatoma cells
topic Animal Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922829/
https://www.ncbi.nlm.nih.gov/pubmed/27333866
http://dx.doi.org/10.12659/MSM.899419
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