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Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings

Epidemiological studies have demonstrated clear associations between specific dietary and environmental risk factors and incidence of colorectal cancer, but the mechanisms responsible for these associations are not known. An animal model could facilitate such an understanding. Both genotoxic and non...

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Autores principales: Yang, Kai, Fard, Sara, Furrer, Rudolf, Archer, Michael C., Bruce, W. Robert, Lip, HoYin, Mehta, Rhea, O'Brien, Peter J., Giacca, Adria, Ward, Wendy E., Femia, A. Pietro, Caderni, Giovanna, Medline, Alan, Banks, Kate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Routledge 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4784512/
https://www.ncbi.nlm.nih.gov/pubmed/26709971
http://dx.doi.org/10.1080/01635581.2016.1115098
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author Yang, Kai
Fard, Sara
Furrer, Rudolf
Archer, Michael C.
Bruce, W. Robert
Lip, HoYin
Mehta, Rhea
O'Brien, Peter J.
Giacca, Adria
Ward, Wendy E.
Femia, A. Pietro
Caderni, Giovanna
Medline, Alan
Banks, Kate
author_facet Yang, Kai
Fard, Sara
Furrer, Rudolf
Archer, Michael C.
Bruce, W. Robert
Lip, HoYin
Mehta, Rhea
O'Brien, Peter J.
Giacca, Adria
Ward, Wendy E.
Femia, A. Pietro
Caderni, Giovanna
Medline, Alan
Banks, Kate
author_sort Yang, Kai
collection PubMed
description Epidemiological studies have demonstrated clear associations between specific dietary and environmental risk factors and incidence of colorectal cancer, but the mechanisms responsible for these associations are not known. An animal model could facilitate such an understanding. Both genotoxic and nongenotoxic carcinogens induce aberrant crypt foci (ACF) in the colons of F344 rats. F344 rats were provided with diets that contained putative risk factors for CRC: low calcium and low vitamin D, high iron, high fructose, and decreased light (UV) exposure or a control diet for 14 wk. The rats were then assessed with biochemical measures and by topological examination for evidence of colon abnormalities. Circulating ionized calcium was decreased from 2.85 to 1.69 mmol/L, and ACF were increased from 0.7 to 13.6 lesions/colon (both P < 0.001). Rats exposed to the multiple environmental conditions associated with colon cancer, developed ACF similar to the heterogeneous or ill-defined ACF in the human colon. Heterogeneous ACF are the most frequently seen in humans and are also seen in rats shortly after exposure to the non-genotoxic colon carcinogen, dextransulfate sodium. The rodent model could be used to assess the pathways from diet and environment to colon cancer and to provide guidance for clinical studies.
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spelling pubmed-47845122016-03-23 Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings Yang, Kai Fard, Sara Furrer, Rudolf Archer, Michael C. Bruce, W. Robert Lip, HoYin Mehta, Rhea O'Brien, Peter J. Giacca, Adria Ward, Wendy E. Femia, A. Pietro Caderni, Giovanna Medline, Alan Banks, Kate Nutr Cancer Original Articles Epidemiological studies have demonstrated clear associations between specific dietary and environmental risk factors and incidence of colorectal cancer, but the mechanisms responsible for these associations are not known. An animal model could facilitate such an understanding. Both genotoxic and nongenotoxic carcinogens induce aberrant crypt foci (ACF) in the colons of F344 rats. F344 rats were provided with diets that contained putative risk factors for CRC: low calcium and low vitamin D, high iron, high fructose, and decreased light (UV) exposure or a control diet for 14 wk. The rats were then assessed with biochemical measures and by topological examination for evidence of colon abnormalities. Circulating ionized calcium was decreased from 2.85 to 1.69 mmol/L, and ACF were increased from 0.7 to 13.6 lesions/colon (both P < 0.001). Rats exposed to the multiple environmental conditions associated with colon cancer, developed ACF similar to the heterogeneous or ill-defined ACF in the human colon. Heterogeneous ACF are the most frequently seen in humans and are also seen in rats shortly after exposure to the non-genotoxic colon carcinogen, dextransulfate sodium. The rodent model could be used to assess the pathways from diet and environment to colon cancer and to provide guidance for clinical studies. Routledge 2016-01-02 2015-12-28 /pmc/articles/PMC4784512/ /pubmed/26709971 http://dx.doi.org/10.1080/01635581.2016.1115098 Text en © 2016 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Original Articles
Yang, Kai
Fard, Sara
Furrer, Rudolf
Archer, Michael C.
Bruce, W. Robert
Lip, HoYin
Mehta, Rhea
O'Brien, Peter J.
Giacca, Adria
Ward, Wendy E.
Femia, A. Pietro
Caderni, Giovanna
Medline, Alan
Banks, Kate
Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings
title Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings
title_full Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings
title_fullStr Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings
title_full_unstemmed Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings
title_short Risk factors for colorectal cancer in man induce aberrant crypt foci in rats: Preliminary findings
title_sort risk factors for colorectal cancer in man induce aberrant crypt foci in rats: preliminary findings
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4784512/
https://www.ncbi.nlm.nih.gov/pubmed/26709971
http://dx.doi.org/10.1080/01635581.2016.1115098
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