Related Experiment Video
Updated: May 25, 2026

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
Potentiation of 1-2-dimethylhydrazine-induced bowel carcinogenesis by the urinary bladder carcinogen
G Steele1, M Chrissey, R Gittes
1Department of Surgery, Division of Urology, Peter Bent Brigham Hospital, Harvard Medical School, Boston, MA 02115, USA.
Abstract:
Male inbred 10-12 week old Wistar/Furth rats received either no carcinogen, or 1-2-dimethylhydrazine (DMH) 20 mg/kg body weight s.c. once weekly for 16 weeks, or N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide (FANFT) 0.2% of the feed for 16 weeks, or DMH and FANFT concurrently. Thirty-three weeks after carcinogen exposure, all surviving treated and control animals were killed and examined for bowel and urinary bladder tumors. Adenocarcinomas of the large and small bowel occurred in approximately 33% of DMH-treated animals, and transitional cell carcinomas of the urinary bladder in approximately 33% of the FANFT-treated animals. After concurrent exposure to both carcinogens, no increased incidence of bladder tumors was noted compared to FANFT treatment alone. However, the number of animals with one or more adenocarcinomas of the bowel (22/30 versus 17/50, p < 0.001), the mean number of tumors per animal (2.1 +/- 0.2 versus 1.1 +/- 0.1, p < 0.01), and the invasiveness of the tumors through the bowel wall were all significantly increased after DMH + FANFT compared to DMH exposure alone.
More Related Videos
Related Concept Videos
Mutagenicity and Carcinogenicity
Physical Properties of Amines
2° Amines to N-Nitrosamines: Reaction with NaNO2
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Spontaneous and Induced Mutations
Basicity of Heterocyclic Aromatic Amines

