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No involvement of Ki-ras or p53 gene mutations in colitis-associated rat colon tumors induced by 1-hydroxyanthraquinone and methylazoxymethanol acetate

✍ 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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✦ 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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