A novel inflammation-related mouse colon carcinogenesis model induced by azoxymethane and dextran sodium sulfate

Cancer Sci. 2003 Nov;94(11):965-73. doi: 10.1111/j.1349-7006.2003.tb01386.x.

Abstract

To develop an efficient animal model for colitis-related carcinogenesis, male Crj: CD-1 (ICR) mice were given a single intraperitoneal administration (10 mg/kg body weight) of a genotoxic colonic carcinogen, azoxymethane (AOM), and a 1-week oral exposure (2% in drinking water) to a non-genotoxic carcinogen, dextran sodium sulfate (DSS), under various protocols. At week 20, colonic neoplasms (adenocarcinomas, 100% incidence with 5.60 +/- 2.42 multiplicity; and adenomas, 38% incidence with 0.20 +/- 0.40 multiplicity) with dysplastic lesions developed in mice treated with AOM followed by DSS. Protocols in which AOM was given during or after DSS administration induced a few tubular adenomas or no tumors in the colon. Immunohistochemical investigation of such dysplasias and neoplasms revealed that all lesions were positive for beta-catenin, cyclooxygenase-2 and inducible nitric oxide synthase, but did not show p53 immunoreactivity. The results indicate that 1-week administration of 2% DSS after initiation with a low dose of AOM exerts a powerful tumor-promoting activity in colon carcinogenesis in male ICR mice, and may provide a novel mouse model for investigating colitis-related colon carcinogenesis and for identifying xenobiotics with modifying effects.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / chemically induced
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Adenoma / chemically induced
  • Adenoma / metabolism
  • Adenoma / pathology
  • Animals
  • Anticoagulants / toxicity
  • Azoxymethane / toxicity*
  • Carcinogens / toxicity*
  • Colitis / chemically induced
  • Colitis / pathology
  • Colonic Neoplasms / chemically induced
  • Colonic Neoplasms / metabolism
  • Colonic Neoplasms / pathology*
  • Cyclooxygenase 2
  • Cytoskeletal Proteins / metabolism
  • Dextran Sulfate / toxicity*
  • Disease Models, Animal
  • Inflammation
  • Injections, Intraperitoneal
  • Isoenzymes / metabolism*
  • Male
  • Mast Cells / metabolism*
  • Mast Cells / pathology
  • Mice
  • Mice, Inbred ICR
  • Nitric Oxide Synthase / metabolism
  • Nitric Oxide Synthase Type II
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • Trans-Activators / metabolism
  • Tumor Suppressor Protein p53 / metabolism
  • beta Catenin

Substances

  • Anticoagulants
  • CTNNB1 protein, mouse
  • Carcinogens
  • Cytoskeletal Proteins
  • Isoenzymes
  • Trans-Activators
  • Tumor Suppressor Protein p53
  • beta Catenin
  • Dextran Sulfate
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Azoxymethane