Literature DB >> 25037416

Anti-tumor properties of orally administered glucosamine and N-acetyl-D-glucosamine oligomers in a mouse model.

Sachie Masuda1, Kazuo Azuma2, Seiji Kurozumi1, Masatoshi Kiyose1, Tomohiro Osaki1, Takeshi Tsuka1, Norihiko Itoh1, Tomohiro Imagawa1, Saburo Minami1, Kimihiko Sato3, Yoshiharu Okamoto4.   

Abstract

The current study evaluated the anti-tumor activities of N-acetyl-d-glucosamine oligomer (NACOS) and glucosamine oligomer (COS) after their oral administration in a tumor (colon 26)-bearing mouse model. Compared to the control group, NACOS and COS groups showed significantly suppressed tumor growth, and apparent, marked apoptosis in tumor tissues. Furthermore, serum interleukin-12p70 and interferon-γ levels significantly increased in the NACOS and COS groups compared to the corresponding levels in the control group. Collectively, the results indicate the oral administration of NACOS and COS could enhance innate immunity. Results of experiments in Myd-88 knockout mice revealed that the apparent effects were related to both Myd-88-dependent and Myd-88-independent pathways. The data indicated that oral administration of NACOS and COS produced anti-tumor effects through the induction of apoptosis and stimulation of the immune system, which suggests that NACOS and COS are candidate anti-tumor functional foods.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Chitin oligosaccharide; Chitosan oligosaccharide; Colon-26; Functional food; Mice; Tumor growth

Mesh:

Substances:

Year:  2014        PMID: 25037416     DOI: 10.1016/j.carbpol.2014.04.102

Source DB:  PubMed          Journal:  Carbohydr Polym        ISSN: 0144-8617            Impact factor:   9.381


  7 in total

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Review 2.  Anticancer and anti-inflammatory properties of chitin and chitosan oligosaccharides.

Authors:  Kazuo Azuma; Tomohiro Osaki; Saburo Minami; Yoshiharu Okamoto
Journal:  J Funct Biomater       Date:  2015-01-14

3.  Chitin Oligosaccharide Modulates Gut Microbiota and Attenuates High-Fat-Diet-Induced Metabolic Syndrome in Mice.

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Journal:  Sci Rep       Date:  2018-02-20       Impact factor: 4.379

5.  High expression of acidic chitinase and chitin digestibility in the stomach of common marmoset (Callithrix jacchus), an insectivorous nonhuman primate.

Authors:  Eri Tabata; Akinori Kashimura; Maiko Uehara; Satoshi Wakita; Masayoshi Sakaguchi; Yasusato Sugahara; Terumi Yurimoto; Erika Sasaki; Vaclav Matoska; Peter O Bauer; Fumitaka Oyama
Journal:  Sci Rep       Date:  2019-01-17       Impact factor: 4.379

6.  Mouse Acidic Chitinase Effectively Degrades Random-Type Chitosan to Chitooligosaccharides of Variable Lengths under Stomach and Lung Tissue pH Conditions.

Authors:  Satoshi Wakita; Yasusato Sugahara; Masayuki Nakamura; Syunsuke Kobayashi; Kazuhisa Matsuda; Chinatsu Takasaki; Masahiro Kimura; Yuta Kida; Maiko Uehara; Eri Tabata; Koji Hiraoka; Shiro Seki; Vaclav Matoska; Peter O Bauer; Fumitaka Oyama
Journal:  Molecules       Date:  2021-11-05       Impact factor: 4.411

7.  Protease resistance of porcine acidic mammalian chitinase under gastrointestinal conditions implies that chitin-containing organisms can be sustainable dietary resources.

Authors:  Eri Tabata; Akinori Kashimura; Satoshi Wakita; Misa Ohno; Masayoshi Sakaguchi; Yasusato Sugahara; Yasutada Imamura; Shiro Seki; Hitoshi Ueda; Vaclav Matoska; Peter O Bauer; Fumitaka Oyama
Journal:  Sci Rep       Date:  2017-10-11       Impact factor: 4.379

  7 in total

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