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Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model

We evaluated the anti-tumor activities of the oral administration of fucoidan extracted from Cladosiphon okamuranus using a tumor (colon 26)-bearing mouse model. The materials used included low-molecular-weight fucoidan (LMWF: 6.5–40 kDa), intermediate-molecular-weight fucoidan (IMWF: 110–138 kDa) a...

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Autores principales: Azuma, Kazuo, Ishihara, Toshitsugu, Nakamoto, Hiroyuki, Amaha, Takao, Osaki, Tomohiro, Tsuka, Takeshi, Imagawa, Tomohiro, Minami, Saburo, Takashima, Osamu, Ifuku, Shinsuke, Morimoto, Minoru, Saimoto, Hiroyuki, Kawamoto, Hitoshi, Okamoto, Yoshiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497027/
https://www.ncbi.nlm.nih.gov/pubmed/23170088
http://dx.doi.org/10.3390/md10102337
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author Azuma, Kazuo
Ishihara, Toshitsugu
Nakamoto, Hiroyuki
Amaha, Takao
Osaki, Tomohiro
Tsuka, Takeshi
Imagawa, Tomohiro
Minami, Saburo
Takashima, Osamu
Ifuku, Shinsuke
Morimoto, Minoru
Saimoto, Hiroyuki
Kawamoto, Hitoshi
Okamoto, Yoshiharu
author_facet Azuma, Kazuo
Ishihara, Toshitsugu
Nakamoto, Hiroyuki
Amaha, Takao
Osaki, Tomohiro
Tsuka, Takeshi
Imagawa, Tomohiro
Minami, Saburo
Takashima, Osamu
Ifuku, Shinsuke
Morimoto, Minoru
Saimoto, Hiroyuki
Kawamoto, Hitoshi
Okamoto, Yoshiharu
author_sort Azuma, Kazuo
collection PubMed
description We evaluated the anti-tumor activities of the oral administration of fucoidan extracted from Cladosiphon okamuranus using a tumor (colon 26)-bearing mouse model. The materials used included low-molecular-weight fucoidan (LMWF: 6.5–40 kDa), intermediate-molecular-weight fucoidan (IMWF: 110–138 kDa) and high-molecular-weight fucoidan (HMWF: 300–330 kDa). The IMWF group showed significantly suppressed tumor growth. The LMWF and HMWF groups showed significantly increased survival times compared with that observed in the control group (mice fed a fucoidan-free diet). The median survival times in the control, LMWF, IMWF and HMWF groups were 23, 46, 40 and 43 days, respectively. It was also found that oral administration of fucoidan increased the population of natural killer cells in the spleen. Furthermore, from the results of the experiment using Myd-88 knockout mice, it was found that these effects are related to gut immunity. These results suggest that fucoidan is a candidate anti-tumor functional food.
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spelling pubmed-34970272012-11-20 Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model Azuma, Kazuo Ishihara, Toshitsugu Nakamoto, Hiroyuki Amaha, Takao Osaki, Tomohiro Tsuka, Takeshi Imagawa, Tomohiro Minami, Saburo Takashima, Osamu Ifuku, Shinsuke Morimoto, Minoru Saimoto, Hiroyuki Kawamoto, Hitoshi Okamoto, Yoshiharu Mar Drugs Article We evaluated the anti-tumor activities of the oral administration of fucoidan extracted from Cladosiphon okamuranus using a tumor (colon 26)-bearing mouse model. The materials used included low-molecular-weight fucoidan (LMWF: 6.5–40 kDa), intermediate-molecular-weight fucoidan (IMWF: 110–138 kDa) and high-molecular-weight fucoidan (HMWF: 300–330 kDa). The IMWF group showed significantly suppressed tumor growth. The LMWF and HMWF groups showed significantly increased survival times compared with that observed in the control group (mice fed a fucoidan-free diet). The median survival times in the control, LMWF, IMWF and HMWF groups were 23, 46, 40 and 43 days, respectively. It was also found that oral administration of fucoidan increased the population of natural killer cells in the spleen. Furthermore, from the results of the experiment using Myd-88 knockout mice, it was found that these effects are related to gut immunity. These results suggest that fucoidan is a candidate anti-tumor functional food. MDPI 2012-10-22 /pmc/articles/PMC3497027/ /pubmed/23170088 http://dx.doi.org/10.3390/md10102337 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Azuma, Kazuo
Ishihara, Toshitsugu
Nakamoto, Hiroyuki
Amaha, Takao
Osaki, Tomohiro
Tsuka, Takeshi
Imagawa, Tomohiro
Minami, Saburo
Takashima, Osamu
Ifuku, Shinsuke
Morimoto, Minoru
Saimoto, Hiroyuki
Kawamoto, Hitoshi
Okamoto, Yoshiharu
Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model
title Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model
title_full Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model
title_fullStr Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model
title_full_unstemmed Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model
title_short Effects of Oral Administration of Fucoidan Extracted from Cladosiphon okamuranus on Tumor Growth and Survival Time in a Tumor-Bearing Mouse Model
title_sort effects of oral administration of fucoidan extracted from cladosiphon okamuranus on tumor growth and survival time in a tumor-bearing mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497027/
https://www.ncbi.nlm.nih.gov/pubmed/23170088
http://dx.doi.org/10.3390/md10102337
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