A rat model for human ulcerative colitis (UC) has been developed by using 1-hydroxyanthraquinone (1-HA) to cause severe inflammation of colonic mucosa. 1-HA also has synergistic effects on the carcinogenicity of methylazoxymethanol (MAM) acetate in the rat colon. In this study, four adenomas and 16
No involvement of Ki-ras or p53 gene mutations in colitis-associated rat colon tumors induced by 1-hydroxyanthraquinone and methylazoxymethanol acetate
β Scribed by Masumi Suzui; Naoki Yoshimi; Toshikazu Ushijima; Yoshinobu Hirose; Hiroki Makita; Aijin Wang; Tshihiko Kawamori; Takuji Tanaka; Hideki Mori; Minako Nagao
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 427 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0899-1987
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β¦ Synopsis
I-Hydroxyanthraquinone (1-HA), which is present in some herbs, and methylazoxymethanol (MAM) acetate, a metabolite o f azoxymethane, show synergistic carcinogenicity in rat colon, and 1 -HA induces ulcerative changes with simultaneous severe inflammation o f the entire colon. In this study, mutations in Ki-ras (exons 1 and 2) and p53 (exons 4-7) were studied by polymerase chain reaction (PCR)-single-strand conformation polymorphism (SSCP) analysis. Of 18 adenomas and 38 adenocarcinomas induced in male F344 rats (52 tumors induced by 1-HA plus M A M acetate, three by 1-HA alone, and one by MAM acetate alone), no mutations in Kiras or p53 were detected under t w o conditions of PCR-SSCP analysis. Because human colon carcinomas from patients with ulcerative colitis have a very low incidence of Ki-ras mutation, this experimental system would be a good animal model o f human colon carcinomas with ulcerative colitis and of human colon carcinomas without Ki-ras or p53 mutations.
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