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Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure

Among cancer diagnoses, colorectal cancer (CRC) is prevalent, with a lifetime risk of developing CRC being approximately 5%. Population variation surrounding the mean risk of developing CRCs has been associated with both inter-individual differences in genomic architecture and environmental exposure...

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Autores principales: Kelly, Scott A., Zhao, Liyang, Jung, Kuo-Chen, Hua, Kunjie, Threadgill, David W., Kim, Yunjung, de Villena, Fernando Pardo Manuel, Pomp, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320535/
https://www.ncbi.nlm.nih.gov/pubmed/28225043
http://dx.doi.org/10.1038/srep43086
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author Kelly, Scott A.
Zhao, Liyang
Jung, Kuo-Chen
Hua, Kunjie
Threadgill, David W.
Kim, Yunjung
de Villena, Fernando Pardo Manuel
Pomp, Daniel
author_facet Kelly, Scott A.
Zhao, Liyang
Jung, Kuo-Chen
Hua, Kunjie
Threadgill, David W.
Kim, Yunjung
de Villena, Fernando Pardo Manuel
Pomp, Daniel
author_sort Kelly, Scott A.
collection PubMed
description Among cancer diagnoses, colorectal cancer (CRC) is prevalent, with a lifetime risk of developing CRC being approximately 5%. Population variation surrounding the mean risk of developing CRCs has been associated with both inter-individual differences in genomic architecture and environmental exposures. Decreased risk of CRC has been associated with physical activity, but protective responses are variable. Here, we utilized a series of experiments to examine the effects of genetic background (strain), voluntary exercise (wheel running), and their interaction on azoxymethane (AOM)-induced intestinal tumor number and size in mice. Additionally, we investigated how the timing of exercise relative to AOM exposure, and amount of exercise, affected tumor number and size. Our results indicated that voluntary exercise significantly reduced tumor number in a strain dependent manner. Additionally, among strains where exercise reduced tumor number (A/J, CC0001/Unc) the timing of voluntary exercise relative to AOM exposure was crucial. Voluntary exercise prior to or during AOM treatment resulted in a significant reduction in tumor number, but exercise following AOM exposure had no effect. The results indicate that voluntary exercise should be used as a preventative measure to reduce risk for environmentally induced CRC with the realization that the extent of protection may depend on genetic background.
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spelling pubmed-53205352017-03-01 Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure Kelly, Scott A. Zhao, Liyang Jung, Kuo-Chen Hua, Kunjie Threadgill, David W. Kim, Yunjung de Villena, Fernando Pardo Manuel Pomp, Daniel Sci Rep Article Among cancer diagnoses, colorectal cancer (CRC) is prevalent, with a lifetime risk of developing CRC being approximately 5%. Population variation surrounding the mean risk of developing CRCs has been associated with both inter-individual differences in genomic architecture and environmental exposures. Decreased risk of CRC has been associated with physical activity, but protective responses are variable. Here, we utilized a series of experiments to examine the effects of genetic background (strain), voluntary exercise (wheel running), and their interaction on azoxymethane (AOM)-induced intestinal tumor number and size in mice. Additionally, we investigated how the timing of exercise relative to AOM exposure, and amount of exercise, affected tumor number and size. Our results indicated that voluntary exercise significantly reduced tumor number in a strain dependent manner. Additionally, among strains where exercise reduced tumor number (A/J, CC0001/Unc) the timing of voluntary exercise relative to AOM exposure was crucial. Voluntary exercise prior to or during AOM treatment resulted in a significant reduction in tumor number, but exercise following AOM exposure had no effect. The results indicate that voluntary exercise should be used as a preventative measure to reduce risk for environmentally induced CRC with the realization that the extent of protection may depend on genetic background. Nature Publishing Group 2017-02-22 /pmc/articles/PMC5320535/ /pubmed/28225043 http://dx.doi.org/10.1038/srep43086 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kelly, Scott A.
Zhao, Liyang
Jung, Kuo-Chen
Hua, Kunjie
Threadgill, David W.
Kim, Yunjung
de Villena, Fernando Pardo Manuel
Pomp, Daniel
Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure
title Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure
title_full Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure
title_fullStr Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure
title_full_unstemmed Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure
title_short Prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure
title_sort prevention of tumorigenesis in mice by exercise is dependent on strain background and timing relative to carcinogen exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320535/
https://www.ncbi.nlm.nih.gov/pubmed/28225043
http://dx.doi.org/10.1038/srep43086
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