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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.
Affiliation
  • Tommelein J; Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Ghent University, Ghent, Belgium.
  • Gremonprez F; Cancer Research Institute Ghent (CRIG), Ghent, Belgium.
  • Verset L; Cancer Research Institute Ghent (CRIG), Ghent, Belgium.
  • De Vlieghere E; Department of Surgery, Ghent University Hospital, Ghent, Belgium.
  • Wagemans G; Department of Pathology, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
  • Gespach C; Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Ghent University, Ghent, Belgium.
  • Boterberg T; Cancer Research Institute Ghent (CRIG), Ghent, Belgium.
  • Demetter P; Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Ghent University, Ghent, Belgium.
  • Ceelen W; Cancer Research Institute Ghent (CRIG), Ghent, Belgium.
  • Bracke M; Institut National de la Santé et de la Recherche Médicale, INSERM, Department of Molecular and Clinical Oncology, Université Paris VI Pierre et Marie Curie, Paris, France.
  • De Wever O; Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Ghent University, Ghent, Belgium.
Oncotarget ; 7(46): 75603-75615, 2016 11 15.
Article de En | MEDLINE | ID: mdl-27689329
ABSTRACT
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.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs colorectales / Prolapsus rectal Type d'étude: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limites: Animals / Female / Humans / Middle aged Langue: En Journal: Oncotarget Année: 2016 Type de document: Article Pays d'affiliation: Belgique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs colorectales / Prolapsus rectal Type d'étude: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limites: Animals / Female / Humans / Middle aged Langue: En Journal: Oncotarget Année: 2016 Type de document: Article Pays d'affiliation: Belgique
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