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Defining the role of polyamines in colon carcinogenesis using mouse models

Genetics and diet are both considered important risk determinants for colorectal cancer, a leading cause of death in the US and worldwide. Genetically engineered mouse (GEM) models have made a significant contribution to the characterization of colorectal cancer risk factors. Reliable, reproducible,...

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Detalles Bibliográficos
Autores principales: Ignatenko, Natalia A., Gerner, Eugene W., Besselsen, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122100/
https://www.ncbi.nlm.nih.gov/pubmed/21712957
http://dx.doi.org/10.4103/1477-3163.79673
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author Ignatenko, Natalia A.
Gerner, Eugene W.
Besselsen, David G.
author_facet Ignatenko, Natalia A.
Gerner, Eugene W.
Besselsen, David G.
author_sort Ignatenko, Natalia A.
collection PubMed
description Genetics and diet are both considered important risk determinants for colorectal cancer, a leading cause of death in the US and worldwide. Genetically engineered mouse (GEM) models have made a significant contribution to the characterization of colorectal cancer risk factors. Reliable, reproducible, and clinically relevant animal models help in the identification of the molecular events associated with disease progression and in the development of effictive treatment strategies. This review is focused on the use of mouse models for studying the role of polyamines in colon carcinogenesis. We describe how the available mouse models of colon cancer such as the multiple intestinal neoplasia (Min) mice and knockout genetic models facilitate understanding of the role of polyamines in colon carcinogenesis and help in the development of a rational strategy for colon cancer chemoprevention.
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spelling pubmed-31221002011-06-27 Defining the role of polyamines in colon carcinogenesis using mouse models Ignatenko, Natalia A. Gerner, Eugene W. Besselsen, David G. J Carcinog Review Article Genetics and diet are both considered important risk determinants for colorectal cancer, a leading cause of death in the US and worldwide. Genetically engineered mouse (GEM) models have made a significant contribution to the characterization of colorectal cancer risk factors. Reliable, reproducible, and clinically relevant animal models help in the identification of the molecular events associated with disease progression and in the development of effictive treatment strategies. This review is focused on the use of mouse models for studying the role of polyamines in colon carcinogenesis. We describe how the available mouse models of colon cancer such as the multiple intestinal neoplasia (Min) mice and knockout genetic models facilitate understanding of the role of polyamines in colon carcinogenesis and help in the development of a rational strategy for colon cancer chemoprevention. Medknow Publications 2011-04-16 /pmc/articles/PMC3122100/ /pubmed/21712957 http://dx.doi.org/10.4103/1477-3163.79673 Text en © 2011 Ignatenko http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ignatenko, Natalia A.
Gerner, Eugene W.
Besselsen, David G.
Defining the role of polyamines in colon carcinogenesis using mouse models
title Defining the role of polyamines in colon carcinogenesis using mouse models
title_full Defining the role of polyamines in colon carcinogenesis using mouse models
title_fullStr Defining the role of polyamines in colon carcinogenesis using mouse models
title_full_unstemmed Defining the role of polyamines in colon carcinogenesis using mouse models
title_short Defining the role of polyamines in colon carcinogenesis using mouse models
title_sort defining the role of polyamines in colon carcinogenesis using mouse models
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122100/
https://www.ncbi.nlm.nih.gov/pubmed/21712957
http://dx.doi.org/10.4103/1477-3163.79673
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