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Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts
In patients with rectal prolapse is the prevalence of colorectal cancer increased, suggesting that a colorectal tumor may induce rectal prolapse. Establishment of tumor xenografts in immunodeficient mice after orthotopic inoculations of human colorectal cancer cells into the caecal wall is a widely...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342764/ https://www.ncbi.nlm.nih.gov/pubmed/27689329 http://dx.doi.org/10.18632/oncotarget.12312 |
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author | Tommelein, Joke Gremonprez, Félix Verset, Laurine De Vlieghere, Elly Wagemans, Glenn Gespach, Christian Boterberg, Tom Demetter, Pieter Ceelen, Wim Bracke, Marc De Wever, Olivier |
author_facet | Tommelein, Joke Gremonprez, Félix Verset, Laurine De Vlieghere, Elly Wagemans, Glenn Gespach, Christian Boterberg, Tom Demetter, Pieter Ceelen, Wim Bracke, Marc De Wever, Olivier |
author_sort | Tommelein, Joke |
collection | PubMed |
description | In patients with rectal prolapse is the prevalence of colorectal cancer increased, suggesting that a colorectal tumor may induce rectal prolapse. Establishment of tumor xenografts in immunodeficient mice after orthotopic inoculations of human colorectal cancer cells into the caecal wall is a widely used approach for the study of human colorectal cancer progression and preclinical evaluation of therapeutics. Remarkably, 70% of young mice carrying a COLO320DM caecal tumor showed symptoms of intussusception of the large bowel associated with intestinal lumen obstruction and rectal prolapse. The quantity of the COLO320DM bioluminescent signal of the first three weeks post-inoculation predicts prolapse in young mice. Rectal prolapse was not observed in adult mice carrying a COLO320DM caecal tumor or young mice carrying a HT29 caecal tumor. In contrast to HT29 tumors, which showed local invasion and metastasis, COLO320DM tumors demonstrated a non-invasive tumor with pushing borders without presence of metastasis. In conclusion, rectal prolapse can be linked to a non-invasive, space-occupying COLO320DM tumor in the gastrointestinal tract of young immunodeficient mice. These data reveal a model that can clarify the association of patients showing rectal prolapse with colorectal cancer. |
format | Online Article Text |
id | pubmed-5342764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53427642017-03-28 Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts Tommelein, Joke Gremonprez, Félix Verset, Laurine De Vlieghere, Elly Wagemans, Glenn Gespach, Christian Boterberg, Tom Demetter, Pieter Ceelen, Wim Bracke, Marc De Wever, Olivier Oncotarget Research Paper In patients with rectal prolapse is the prevalence of colorectal cancer increased, suggesting that a colorectal tumor may induce rectal prolapse. Establishment of tumor xenografts in immunodeficient mice after orthotopic inoculations of human colorectal cancer cells into the caecal wall is a widely used approach for the study of human colorectal cancer progression and preclinical evaluation of therapeutics. Remarkably, 70% of young mice carrying a COLO320DM caecal tumor showed symptoms of intussusception of the large bowel associated with intestinal lumen obstruction and rectal prolapse. The quantity of the COLO320DM bioluminescent signal of the first three weeks post-inoculation predicts prolapse in young mice. Rectal prolapse was not observed in adult mice carrying a COLO320DM caecal tumor or young mice carrying a HT29 caecal tumor. In contrast to HT29 tumors, which showed local invasion and metastasis, COLO320DM tumors demonstrated a non-invasive tumor with pushing borders without presence of metastasis. In conclusion, rectal prolapse can be linked to a non-invasive, space-occupying COLO320DM tumor in the gastrointestinal tract of young immunodeficient mice. These data reveal a model that can clarify the association of patients showing rectal prolapse with colorectal cancer. Impact Journals LLC 2016-09-28 /pmc/articles/PMC5342764/ /pubmed/27689329 http://dx.doi.org/10.18632/oncotarget.12312 Text en Copyright: © 2016 Tommelein et al. http://creativecommons.org/licenses/by/3.0/ 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 credited. |
spellingShingle | Research Paper Tommelein, Joke Gremonprez, Félix Verset, Laurine De Vlieghere, Elly Wagemans, Glenn Gespach, Christian Boterberg, Tom Demetter, Pieter Ceelen, Wim Bracke, Marc De Wever, Olivier Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts |
title | Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts |
title_full | Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts |
title_fullStr | Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts |
title_full_unstemmed | Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts |
title_short | Age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts |
title_sort | age and cellular context influence rectal prolapse formation in mice with caecal wall colorectal cancer xenografts |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342764/ https://www.ncbi.nlm.nih.gov/pubmed/27689329 http://dx.doi.org/10.18632/oncotarget.12312 |
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