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Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis
Many observational epidemiologic studies suggest an association between exercise and colon cancer risk. The mechanisms contributing to a preventative effect of exercise on colon cancer are complex and multifaceted. Altered immune system function is one possible mechanism that has been largely unexpl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432723/ https://www.ncbi.nlm.nih.gov/pubmed/24859893 http://dx.doi.org/10.3892/ijo.2014.2457 |
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author | McCLELLAN, JAMIE L. STEINER, JENNIFER L. DAY, STANI D. ENOS, REILLY T. DAVIS, MARK J. SINGH, UDAI P. MURPHY, E. ANGELA |
author_facet | McCLELLAN, JAMIE L. STEINER, JENNIFER L. DAY, STANI D. ENOS, REILLY T. DAVIS, MARK J. SINGH, UDAI P. MURPHY, E. ANGELA |
author_sort | McCLELLAN, JAMIE L. |
collection | PubMed |
description | Many observational epidemiologic studies suggest an association between exercise and colon cancer risk. The mechanisms contributing to a preventative effect of exercise on colon cancer are complex and multifaceted. Altered immune system function is one possible mechanism that has been largely unexplored. Therefore, the purpose of this study was to examine the effects of exercise on markers associated with macrophages and select T cell populations in a mouse model of intestinal tumorigenesis and to relate this to polyp characteristics. Male Apc(Min)(/+) mice were randomly assigned to either sedentary (Sed) or exercise (Ex) treatment (n=6–9/group). The exercise treatment consisted of treadmill running for 1 h/day and 6 days a week at 15 m/min from 4 until 16 weeks of age. Intestinal polyps were counted and categorized by size. Mucosal tissue was analyzed for mRNA expression of overall macrophages (F4/80), for genes associated with M1 (IL-12, IL-23 and Nos2) and M2 (CD206, IL-10, IL-4, CCL17, CCL22 and Arg-1) macrophages and the macrophage chemoattractants MCP-1, fetuin A and CXCL14. Markers for cytotoxic T cells (CTLs) and regulatory T cells were also examined by measuring mRNA expression of CD8 and Foxp3, respectively. While there was no significant difference in overall polyp number between the groups (Sed, 23.3±4.3; and Ex, 16.5±4.3), Ex did have a reduction in the number of large polyps (Sed, 6.1±1.1; and Ex, 3.0±0.6) (P<0.05). This was consistent with a decrease in spleen weight (P<0.05). Similarly, Ex reduced mRNA expression of overall macrophages (F4/80) as well as markers associated with both M1 (IL-12) and M2 (CD206, CCL22 and Arg-1) subtypes (P<0.05) but there was no significant decrease in macrophage chemoattractants. CD8 expression was increased while Foxp3 expression was decreased with Ex (P<0.05). Overall the data provide important new information on immune regulation as a possible mechanism for the documented benefits of exercise training on reducing colon cancer progression. |
format | Online Article Text |
id | pubmed-4432723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-44327232015-08-01 Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis McCLELLAN, JAMIE L. STEINER, JENNIFER L. DAY, STANI D. ENOS, REILLY T. DAVIS, MARK J. SINGH, UDAI P. MURPHY, E. ANGELA Int J Oncol Articles Many observational epidemiologic studies suggest an association between exercise and colon cancer risk. The mechanisms contributing to a preventative effect of exercise on colon cancer are complex and multifaceted. Altered immune system function is one possible mechanism that has been largely unexplored. Therefore, the purpose of this study was to examine the effects of exercise on markers associated with macrophages and select T cell populations in a mouse model of intestinal tumorigenesis and to relate this to polyp characteristics. Male Apc(Min)(/+) mice were randomly assigned to either sedentary (Sed) or exercise (Ex) treatment (n=6–9/group). The exercise treatment consisted of treadmill running for 1 h/day and 6 days a week at 15 m/min from 4 until 16 weeks of age. Intestinal polyps were counted and categorized by size. Mucosal tissue was analyzed for mRNA expression of overall macrophages (F4/80), for genes associated with M1 (IL-12, IL-23 and Nos2) and M2 (CD206, IL-10, IL-4, CCL17, CCL22 and Arg-1) macrophages and the macrophage chemoattractants MCP-1, fetuin A and CXCL14. Markers for cytotoxic T cells (CTLs) and regulatory T cells were also examined by measuring mRNA expression of CD8 and Foxp3, respectively. While there was no significant difference in overall polyp number between the groups (Sed, 23.3±4.3; and Ex, 16.5±4.3), Ex did have a reduction in the number of large polyps (Sed, 6.1±1.1; and Ex, 3.0±0.6) (P<0.05). This was consistent with a decrease in spleen weight (P<0.05). Similarly, Ex reduced mRNA expression of overall macrophages (F4/80) as well as markers associated with both M1 (IL-12) and M2 (CD206, CCL22 and Arg-1) subtypes (P<0.05) but there was no significant decrease in macrophage chemoattractants. CD8 expression was increased while Foxp3 expression was decreased with Ex (P<0.05). Overall the data provide important new information on immune regulation as a possible mechanism for the documented benefits of exercise training on reducing colon cancer progression. D.A. Spandidos 2014-05-22 /pmc/articles/PMC4432723/ /pubmed/24859893 http://dx.doi.org/10.3892/ijo.2014.2457 Text en Copyright © 2014, 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 McCLELLAN, JAMIE L. STEINER, JENNIFER L. DAY, STANI D. ENOS, REILLY T. DAVIS, MARK J. SINGH, UDAI P. MURPHY, E. ANGELA Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis |
title | Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis |
title_full | Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis |
title_fullStr | Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis |
title_full_unstemmed | Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis |
title_short | Exercise effects on polyp burden and immune markers in the Apc(Min)(/+) mouse model of intestinal tumorigenesis |
title_sort | exercise effects on polyp burden and immune markers in the apc(min)(/+) mouse model of intestinal tumorigenesis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432723/ https://www.ncbi.nlm.nih.gov/pubmed/24859893 http://dx.doi.org/10.3892/ijo.2014.2457 |
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