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Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer
BACKGROUND: Colorectal-cancer (CRC) research has greatly benefited from the availability of small animal tumor models. Spontaneous and chemically-induced CRC models are widely used yet limited in their resemblance to human disease and are often prolonged, not accurately repetitive, and associated wi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236220/ https://www.ncbi.nlm.nih.gov/pubmed/22174916 http://dx.doi.org/10.1371/journal.pone.0028858 |
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author | Zigmond, Ehud Halpern, Zamir Elinav, Eran Brazowski, Eli Jung, Steffen Varol, Chen |
author_facet | Zigmond, Ehud Halpern, Zamir Elinav, Eran Brazowski, Eli Jung, Steffen Varol, Chen |
author_sort | Zigmond, Ehud |
collection | PubMed |
description | BACKGROUND: Colorectal-cancer (CRC) research has greatly benefited from the availability of small animal tumor models. Spontaneous and chemically-induced CRC models are widely used yet limited in their resemblance to human disease and are often prolonged, not accurately repetitive, and associated with inflammatory side effects. In-situ murine or human tumor implantation in the gastrointestinal tract of mice is extremely challenging, and limited by inter-animal variability and procedure-related complications and mortality. As a result, in frequent studies CRC is implanted in distal sites, most commonly the subcutaneous region, an approach that is greatly limited by the absence of normal gastrointestinal tumor milieu and has substantial effects on tumor development. AIMS: In this study we aimed to develop a well-tolerated repetitive tool to study CRC in small animals by adapting the murine colonoscopy system to serve as a platform for colonic sub-mucosal orthotopic implantation of human and murine CRC tumor cells. RESULTS: We report the establishment of a novel small-animal CRC model that is minimally invasive, rapid, well-tolerated, highly reproducible, and confers precise control of tumor number, location and growth rate. Moreover, we show that this model uniquely allows the side-by-side induction of distinct genetically manipulated tumors, enabling the mechanistic study of tumor interaction and cross-talk within the native intestinal microenvironment. CONCLUSIONS: Employment of this new approach may represent a major technical advance for the in-vivo study of CRC. |
format | Online Article Text |
id | pubmed-3236220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32362202011-12-15 Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer Zigmond, Ehud Halpern, Zamir Elinav, Eran Brazowski, Eli Jung, Steffen Varol, Chen PLoS One Research Article BACKGROUND: Colorectal-cancer (CRC) research has greatly benefited from the availability of small animal tumor models. Spontaneous and chemically-induced CRC models are widely used yet limited in their resemblance to human disease and are often prolonged, not accurately repetitive, and associated with inflammatory side effects. In-situ murine or human tumor implantation in the gastrointestinal tract of mice is extremely challenging, and limited by inter-animal variability and procedure-related complications and mortality. As a result, in frequent studies CRC is implanted in distal sites, most commonly the subcutaneous region, an approach that is greatly limited by the absence of normal gastrointestinal tumor milieu and has substantial effects on tumor development. AIMS: In this study we aimed to develop a well-tolerated repetitive tool to study CRC in small animals by adapting the murine colonoscopy system to serve as a platform for colonic sub-mucosal orthotopic implantation of human and murine CRC tumor cells. RESULTS: We report the establishment of a novel small-animal CRC model that is minimally invasive, rapid, well-tolerated, highly reproducible, and confers precise control of tumor number, location and growth rate. Moreover, we show that this model uniquely allows the side-by-side induction of distinct genetically manipulated tumors, enabling the mechanistic study of tumor interaction and cross-talk within the native intestinal microenvironment. CONCLUSIONS: Employment of this new approach may represent a major technical advance for the in-vivo study of CRC. Public Library of Science 2011-12-12 /pmc/articles/PMC3236220/ /pubmed/22174916 http://dx.doi.org/10.1371/journal.pone.0028858 Text en This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zigmond, Ehud Halpern, Zamir Elinav, Eran Brazowski, Eli Jung, Steffen Varol, Chen Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer |
title | Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer |
title_full | Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer |
title_fullStr | Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer |
title_full_unstemmed | Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer |
title_short | Utilization of Murine Colonoscopy for Orthotopic Implantation of Colorectal Cancer |
title_sort | utilization of murine colonoscopy for orthotopic implantation of colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236220/ https://www.ncbi.nlm.nih.gov/pubmed/22174916 http://dx.doi.org/10.1371/journal.pone.0028858 |
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