4.7 Article

AOM/DSS Induced Colitis-Associated Colorectal Cancer in 14-Month-Old Female Balb/C and C57/Bl6 Mice-A Pilot Study

Journal

Publisher

MDPI
DOI: 10.3390/ijms23095278

Keywords

aged mice; colitis associated colorectal cancer; AOM; DSS; mouse strain differences; pilot study

Funding

  1. Austrian Science Fund (FWF)
  2. Herzfelder'sche Familienstiftung [P 32840-B]
  3. Austrian Science Fund (FWF) [P 29948-B28, P35069-B, DOC 59-833]
  4. Austrian Science Fund (FWF) [P35069] Funding Source: Austrian Science Fund (FWF)

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Colitis is a significant risk factor for the development of colorectal cancer, and the azoxymethane-dextran sulphate-sodium (AOM/DSS) model is commonly used to study colitis-associated colorectal cancer (CAC). This study conducted a pilot study using 14-month-old Balb/C and C57/Bl6 mice to induce CAC with different concentrations of DSS. The results showed that the DSS dose was correlated with the development of CAC, but different mouse strains had varied responses to the induction. The optimal conditions for CAC induction were found to be 3% DSS, except for Balb/C mice which reacted severely to this concentration. Therefore, 2.5% DSS may be more suitable for future experiments comparing CAC in aged Balb/C and C57/Bl6 mice.
Colitis is a major risk factor for the development of colorectal cancer, leading to colitis-associated colorectal cancer (CAC). The most commonly used animal model to study CAC is the azoxymethane-dextran sulphate-sodium (AOM/DSS) model. The ideal experimental conditions of this model depend on several factors, including the used mouse strain. No data on feasibility and conditions for older mice, e.g., for aging studies, have yet been reported. Thus, we conducted a descriptive, observational pilot study where CAC was induced in 14-month-old female Balb/C and C57/Bl6 mice using 12.5 mg/kg AOM i.p. and three different concentrations of DSS (1, 2, and 3%) in drinking water (ad. lib.). The mice were monitored regularly during the three-month experimental phase. After euthanasia, the colons of the mice were evaluated macroscopically and microscopically. Both the mouse strains showed a DSS-concentration-dependent induction of CAC. Carcinomas were only observed at 3% DSS. The DSS dose was found to be significantly correlated with the histology score and % Ki67 positive cells only in C57/Bl6 mice but not in Balb/C mice, which showed a variable response to the CAC induction. No differences in colon length, weight, or mucin content were observed. Optimal conditions for CAC induction in these aged animals are thus considered to be 3% DSS, as carcinomas did not develop when 2% DSS was used. On the other hand, Balb/C mice reacted severely to 3% DSS, indicating that 2.5% DSS may be the sweet spot for future experiments comparing CAC in aged Balb/C and C57/Bl6 mice. This model will allow investigation of the effect of aging on CAC development and therapy.

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