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Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation
(1) Background: Colorectal cancer (CRC) is among the best examples of the relationship between inflammation and increased cancer risk. (2) Methods: To examine the effects of spontaneous low-grade chronic inflammation on the pathogenesis of CRC, we developed a new murine model of colitis-associated c...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215554/ https://www.ncbi.nlm.nih.gov/pubmed/32340123 http://dx.doi.org/10.3390/ijms21082972 |
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author | De Santis, Stefania Verna, Giulio Serino, Grazia Armentano, Raffaele Cavalcanti, Elisabetta Liso, Marina Dicarlo, Manuela Coletta, Sergio Mastronardi, Mauro Lippolis, Antonio Tafaro, Angela Santino, Angelo Pinto, Aldo Campiglia, Pietro Huang, Alex Y. Cominelli, Fabio Pizarro, Theresa T. Chieppa, Marcello |
author_facet | De Santis, Stefania Verna, Giulio Serino, Grazia Armentano, Raffaele Cavalcanti, Elisabetta Liso, Marina Dicarlo, Manuela Coletta, Sergio Mastronardi, Mauro Lippolis, Antonio Tafaro, Angela Santino, Angelo Pinto, Aldo Campiglia, Pietro Huang, Alex Y. Cominelli, Fabio Pizarro, Theresa T. Chieppa, Marcello |
author_sort | De Santis, Stefania |
collection | PubMed |
description | (1) Background: Colorectal cancer (CRC) is among the best examples of the relationship between inflammation and increased cancer risk. (2) Methods: To examine the effects of spontaneous low-grade chronic inflammation on the pathogenesis of CRC, we developed a new murine model of colitis-associated cancer (CAC) by crossing Mucin 2 mutated mice (Winnie) with Apc(Min/+) mice. (3) Results: The resulting Winnie-Apc(Min/+) model combines an inflammatory background with a genetic predisposition to small intestinal polyposis. Winnie-Apc(Min/+) mice show an early occurrence of inflammatory signs and dysplastic lesions in the distal colon with a specific molecular signature. (4) Conclusion: The Winnie-Apc(Min/+) model is a perfect model to demonstrate that chronic inflammation represents a crucial risk factor for the onset and progression of tumoral lesions in individuals genetically predisposed to CRC. |
format | Online Article Text |
id | pubmed-7215554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72155542020-05-22 Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation De Santis, Stefania Verna, Giulio Serino, Grazia Armentano, Raffaele Cavalcanti, Elisabetta Liso, Marina Dicarlo, Manuela Coletta, Sergio Mastronardi, Mauro Lippolis, Antonio Tafaro, Angela Santino, Angelo Pinto, Aldo Campiglia, Pietro Huang, Alex Y. Cominelli, Fabio Pizarro, Theresa T. Chieppa, Marcello Int J Mol Sci Article (1) Background: Colorectal cancer (CRC) is among the best examples of the relationship between inflammation and increased cancer risk. (2) Methods: To examine the effects of spontaneous low-grade chronic inflammation on the pathogenesis of CRC, we developed a new murine model of colitis-associated cancer (CAC) by crossing Mucin 2 mutated mice (Winnie) with Apc(Min/+) mice. (3) Results: The resulting Winnie-Apc(Min/+) model combines an inflammatory background with a genetic predisposition to small intestinal polyposis. Winnie-Apc(Min/+) mice show an early occurrence of inflammatory signs and dysplastic lesions in the distal colon with a specific molecular signature. (4) Conclusion: The Winnie-Apc(Min/+) model is a perfect model to demonstrate that chronic inflammation represents a crucial risk factor for the onset and progression of tumoral lesions in individuals genetically predisposed to CRC. MDPI 2020-04-23 /pmc/articles/PMC7215554/ /pubmed/32340123 http://dx.doi.org/10.3390/ijms21082972 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article De Santis, Stefania Verna, Giulio Serino, Grazia Armentano, Raffaele Cavalcanti, Elisabetta Liso, Marina Dicarlo, Manuela Coletta, Sergio Mastronardi, Mauro Lippolis, Antonio Tafaro, Angela Santino, Angelo Pinto, Aldo Campiglia, Pietro Huang, Alex Y. Cominelli, Fabio Pizarro, Theresa T. Chieppa, Marcello Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation |
title | Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation |
title_full | Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation |
title_fullStr | Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation |
title_full_unstemmed | Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation |
title_short | Winnie-APC(Min/+) Mice: A Spontaneous Model of Colitis-Associated Colorectal Cancer Combining Genetics and Inflammation |
title_sort | winnie-apc(min/+) mice: a spontaneous model of colitis-associated colorectal cancer combining genetics and inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215554/ https://www.ncbi.nlm.nih.gov/pubmed/32340123 http://dx.doi.org/10.3390/ijms21082972 |
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