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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...

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Autores principales: Tommelein, Joke, Gremonprez, Félix, Verset, Laurine, De Vlieghere, Elly, Wagemans, Glenn, Gespach, Christian, Boterberg, Tom, Demetter, Pieter, Ceelen, Wim, Bracke, Marc, De Wever, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
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.
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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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