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Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency

Chitosan and Agaricus blazei Murill (ABM) extracts possess antitumor activities. The aim of the present study was to investigate whether chitosan, ABM extract or the two in combination were effective against tumors in tumor-bearing mice. The mice were subcutaneously injected with SK-Hep 1 cells and...

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Autores principales: YEH, MING YANG, SHANG, HUNG SHENG, LU, HSU FENG, CHOU, JASON, YEH, CHUN, CHANG, JIN BIOU, HUNG, HSIAO FANG, KUO, WAN LIN, WU, LUNG YUAN, CHUNG, JING GUNG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438976/
https://www.ncbi.nlm.nih.gov/pubmed/25760985
http://dx.doi.org/10.3892/mmr.2015.3454
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author YEH, MING YANG
SHANG, HUNG SHENG
LU, HSU FENG
CHOU, JASON
YEH, CHUN
CHANG, JIN BIOU
HUNG, HSIAO FANG
KUO, WAN LIN
WU, LUNG YUAN
CHUNG, JING GUNG
author_facet YEH, MING YANG
SHANG, HUNG SHENG
LU, HSU FENG
CHOU, JASON
YEH, CHUN
CHANG, JIN BIOU
HUNG, HSIAO FANG
KUO, WAN LIN
WU, LUNG YUAN
CHUNG, JING GUNG
author_sort YEH, MING YANG
collection PubMed
description Chitosan and Agaricus blazei Murill (ABM) extracts possess antitumor activities. The aim of the present study was to investigate whether chitosan, ABM extract or the two in combination were effective against tumors in tumor-bearing mice. The mice were subcutaneously injected with SK-Hep 1 cells and were then were divided into the following six groups: Group 1, control group; group 2, chitosan 5 mg/kg/day; group 3, chitosan 20 mg/kg/day; group 4, ABM (246 mg/kg/day) and chitosan (5 mg/kg/day) combined; group 5, ABM (984 mg/kg/day) and chitosan (20 mg/kg/day) combined; and group 6, ABM (984 mg/kg/day). The mice were treated with the different concentrations of chitosan, ABM or combinations of the two for 6 weeks. The levels of glutamic oxaloacetic transaminase (GOT), glutamic pyruvic transaminase (GPT) and vascular endothelial growth factor (VEGF), and tissue histopathological features were examined in the surviving animals. Based on the results of the investigation, the treatments performed in groups 2, 3 and 4 were identified as being capable of reducing the weights of the tumors, however, group 4, which was treated with chitosan (5 mg/kg/day) in combination with ABM (246 mg/kg/day) was able to reduce the levels of GOT and VEGF. As a result, treatment with chitosan in combination with ABM may offer potential in cancer therapy and requires further investigation.
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spelling pubmed-44389762015-06-05 Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency YEH, MING YANG SHANG, HUNG SHENG LU, HSU FENG CHOU, JASON YEH, CHUN CHANG, JIN BIOU HUNG, HSIAO FANG KUO, WAN LIN WU, LUNG YUAN CHUNG, JING GUNG Mol Med Rep Articles Chitosan and Agaricus blazei Murill (ABM) extracts possess antitumor activities. The aim of the present study was to investigate whether chitosan, ABM extract or the two in combination were effective against tumors in tumor-bearing mice. The mice were subcutaneously injected with SK-Hep 1 cells and were then were divided into the following six groups: Group 1, control group; group 2, chitosan 5 mg/kg/day; group 3, chitosan 20 mg/kg/day; group 4, ABM (246 mg/kg/day) and chitosan (5 mg/kg/day) combined; group 5, ABM (984 mg/kg/day) and chitosan (20 mg/kg/day) combined; and group 6, ABM (984 mg/kg/day). The mice were treated with the different concentrations of chitosan, ABM or combinations of the two for 6 weeks. The levels of glutamic oxaloacetic transaminase (GOT), glutamic pyruvic transaminase (GPT) and vascular endothelial growth factor (VEGF), and tissue histopathological features were examined in the surviving animals. Based on the results of the investigation, the treatments performed in groups 2, 3 and 4 were identified as being capable of reducing the weights of the tumors, however, group 4, which was treated with chitosan (5 mg/kg/day) in combination with ABM (246 mg/kg/day) was able to reduce the levels of GOT and VEGF. As a result, treatment with chitosan in combination with ABM may offer potential in cancer therapy and requires further investigation. D.A. Spandidos 2015-07 2015-03-09 /pmc/articles/PMC4438976/ /pubmed/25760985 http://dx.doi.org/10.3892/mmr.2015.3454 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
YEH, MING YANG
SHANG, HUNG SHENG
LU, HSU FENG
CHOU, JASON
YEH, CHUN
CHANG, JIN BIOU
HUNG, HSIAO FANG
KUO, WAN LIN
WU, LUNG YUAN
CHUNG, JING GUNG
Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency
title Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency
title_full Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency
title_fullStr Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency
title_full_unstemmed Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency
title_short Chitosan oligosaccharides in combination with Agaricus blazei Murill extract reduces hepatoma formation in mice with severe combined immunodeficiency
title_sort chitosan oligosaccharides in combination with agaricus blazei murill extract reduces hepatoma formation in mice with severe combined immunodeficiency
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438976/
https://www.ncbi.nlm.nih.gov/pubmed/25760985
http://dx.doi.org/10.3892/mmr.2015.3454
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