Cargando…
A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice
PURPOSE: This study aimed to investigate the potential antitumor effects and mechanisms underlying the action of a functional food containing 55 different natural food ingredients. MATERIALS AND METHODS: Azoxymethane/dextran sulfate sodium was used to establish a mouse model of colorectal cancer. Se...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924130/ https://www.ncbi.nlm.nih.gov/pubmed/33664579 http://dx.doi.org/10.2147/OTT.S283465 |
_version_ | 1783659027915341824 |
---|---|
author | Zhang, Jie Chen, Zhewen Lu, Yanwen Tu, Daoyuan Zou, Fengqian Lin, Shouwen Yu, Weinan Miao, Mingyong Shi, Hanping |
author_facet | Zhang, Jie Chen, Zhewen Lu, Yanwen Tu, Daoyuan Zou, Fengqian Lin, Shouwen Yu, Weinan Miao, Mingyong Shi, Hanping |
author_sort | Zhang, Jie |
collection | PubMed |
description | PURPOSE: This study aimed to investigate the potential antitumor effects and mechanisms underlying the action of a functional food containing 55 different natural food ingredients. MATERIALS AND METHODS: Azoxymethane/dextran sulfate sodium was used to establish a mouse model of colorectal cancer. Serum levels of cytokines, diamine oxidase, D-lactate, and endotoxin were measured using enzyme-linked immunosorbent assays. Immune cells from the mouse spleen and tumor tissue were analyzed by flow cytometry. Finally, 16S rRNA gene sequencing and liquid chromatography–mass spectrometry were used to study the fecal microbiota and microbial metabolites, respectively. RESULTS: The tumor growth was significantly lower in the FFD group than in the model group. The intestinal barrier function, fat mass, and lean body mass were significantly improved in the FFD group compared with the model group. The levels of interleukin-6 and tumor necrosis factor-α were significantly lower in the FFD group, while the proportions of total T cells, CD3(+)CD4(+), CD3(+)CD8(+), and interferon-γ-producing CD4(+) T cells were significantly higher. Analysis of the diversity of the gut microbiota identified 60 differential bacterial genera between the FFD and model groups, with lower abundances of Desulfovibrio and unclassified Ruminococcaceae and higher abundances of the beneficial bacterial genera Bacteroides and Parasutterella in the FFD group. The fecal metabolite analysis revealed 635 differential metabolites between the FFD and model groups, with lower levels of deuteroporphyrin IX and citrulline and higher levels of acetic acid and ascorbic acid in the FFD group. CONCLUSION: Our results demonstrate that the functional food tested can inhibit the growth of colorectal cancer. This effect may be due to the ability of this food to improve nutritional status, enhance intestinal barrier function, and regulate the tumor microenvironment via changes in the intestinal microbiota and metabolites. |
format | Online Article Text |
id | pubmed-7924130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-79241302021-03-03 A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice Zhang, Jie Chen, Zhewen Lu, Yanwen Tu, Daoyuan Zou, Fengqian Lin, Shouwen Yu, Weinan Miao, Mingyong Shi, Hanping Onco Targets Ther Original Research PURPOSE: This study aimed to investigate the potential antitumor effects and mechanisms underlying the action of a functional food containing 55 different natural food ingredients. MATERIALS AND METHODS: Azoxymethane/dextran sulfate sodium was used to establish a mouse model of colorectal cancer. Serum levels of cytokines, diamine oxidase, D-lactate, and endotoxin were measured using enzyme-linked immunosorbent assays. Immune cells from the mouse spleen and tumor tissue were analyzed by flow cytometry. Finally, 16S rRNA gene sequencing and liquid chromatography–mass spectrometry were used to study the fecal microbiota and microbial metabolites, respectively. RESULTS: The tumor growth was significantly lower in the FFD group than in the model group. The intestinal barrier function, fat mass, and lean body mass were significantly improved in the FFD group compared with the model group. The levels of interleukin-6 and tumor necrosis factor-α were significantly lower in the FFD group, while the proportions of total T cells, CD3(+)CD4(+), CD3(+)CD8(+), and interferon-γ-producing CD4(+) T cells were significantly higher. Analysis of the diversity of the gut microbiota identified 60 differential bacterial genera between the FFD and model groups, with lower abundances of Desulfovibrio and unclassified Ruminococcaceae and higher abundances of the beneficial bacterial genera Bacteroides and Parasutterella in the FFD group. The fecal metabolite analysis revealed 635 differential metabolites between the FFD and model groups, with lower levels of deuteroporphyrin IX and citrulline and higher levels of acetic acid and ascorbic acid in the FFD group. CONCLUSION: Our results demonstrate that the functional food tested can inhibit the growth of colorectal cancer. This effect may be due to the ability of this food to improve nutritional status, enhance intestinal barrier function, and regulate the tumor microenvironment via changes in the intestinal microbiota and metabolites. Dove 2021-02-26 /pmc/articles/PMC7924130/ /pubmed/33664579 http://dx.doi.org/10.2147/OTT.S283465 Text en © 2021 Zhang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Zhang, Jie Chen, Zhewen Lu, Yanwen Tu, Daoyuan Zou, Fengqian Lin, Shouwen Yu, Weinan Miao, Mingyong Shi, Hanping A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice |
title | A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice |
title_full | A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice |
title_fullStr | A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice |
title_full_unstemmed | A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice |
title_short | A Functional Food Inhibits Azoxymethane/Dextran Sulfate Sodium-Induced Inflammatory Colorectal Cancer in Mice |
title_sort | functional food inhibits azoxymethane/dextran sulfate sodium-induced inflammatory colorectal cancer in mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924130/ https://www.ncbi.nlm.nih.gov/pubmed/33664579 http://dx.doi.org/10.2147/OTT.S283465 |
work_keys_str_mv | AT zhangjie afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT chenzhewen afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT luyanwen afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT tudaoyuan afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT zoufengqian afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT linshouwen afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT yuweinan afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT miaomingyong afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT shihanping afunctionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT zhangjie functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT chenzhewen functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT luyanwen functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT tudaoyuan functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT zoufengqian functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT linshouwen functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT yuweinan functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT miaomingyong functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice AT shihanping functionalfoodinhibitsazoxymethanedextransulfatesodiuminducedinflammatorycolorectalcancerinmice |