RARE FREQUENCY OF ACTIVATION OF THE KI-RAS GENE IN RAT COLON TUMORS INDUCED BY HETEROCYCLIC AMINES - POSSIBLE ALTERNATIVE MECHANISMS OF HUMAN COLON CARCINOGENESIS

被引:36
作者
KAKIUCHI, H
USHIJIMA, T
OCHIAI, M
IMAI, K
ITO, N
YACHI, A
SUGIMURA, T
NAGAO, M
机构
[1] NATL CANC CTR,DIV CARCINOGENESIS,1-1 TSUKIJI 5 CHOME,CHUO KU,TOKYO 104,JAPAN
[2] SAPPORO MED COLL,DIV INTERNAL MED 1,SAPPORO,HOKKAIDO 060,JAPAN
[3] NAGOYA CITY UNIV,SCH MED,DEPT PATHOL 1,NAGOYA,AICHI 467,JAPAN
关键词
RAT COLON CARCINOMA; RAS GENE; HETEROCYCLIC AMINE;
D O I
10.1002/mc.2940080110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heterocyclic amines present in cooked foods are known to produce colon tumors in F344 rats at a high incidence, indicating the possibility of involvement of ras gene activation in colon carcinogenesis in rats as in humans. We examined mutations at codons 12, 13, and 61 of the Ki-ras, Ha-ras, and N-ras genes by polymerase chain reaction-direct sequencing in seven colon tumors in F344 rats induced by 2-amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1), 11 induced by 2-amino-3-methylimidazo[4,5-f]quinoline, and nine induced by 2-amino-1 -methyl-6-phenylimidazo[4,5-b]pyridine. A Ki-ras gene mutation (G --> T at the second position in codon 12) was found in one Glu-P-1-induced colon adenocarcinoma. None of the other 26 tumors had mutations in any of these three ras family genes. These results indicate that in rats, colon carcinogenesis induced by heterocyclic amines may be induced by alterations of other oncogenes or tumor suppressor genes. We think this experimental system using carcinogens to which humans are exposed is a good model for studying alterations of other genes in human colon tumors in which no Ki-ras alterations are observed. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:44 / 48
页数:5
相关论文
共 43 条
[31]  
SHIKE M, 1990, B WORLD HEALTH ORGAN, V68, P377
[32]  
SHIRAI T, IN PRESS HETEROCYCLI
[33]   REACTION OF N-HYDROXYLAMINE AND N-ACETOXY DERIVATIVES OF 2-AMINO-3-METHYLIMIDAZOLO[4,5-F]QUINOLINE WITH DNA - SYNTHESIS AND IDENTIFICATION OF N-(DEOXYGUANOSIN-8-YL)-IQ [J].
SNYDERWINE, EG ;
ROLLER, PP ;
ADAMSON, RH ;
SATO, S ;
THORGEIRSSON, SS .
CARCINOGENESIS, 1988, 9 (06) :1061-1065
[34]   EVIDENCE FOR A RAS GENE MUTATION IN AZOXYMETHANE-INDUCED COLONIC ABERRANT CRYPTS IN SPRAGUE-DAWLEY RATS - EARLIEST RECOGNIZABLE PRECURSOR LESIONS OF EXPERIMENTAL COLON CANCER [J].
STOPERA, SA ;
MURPHY, LC ;
BIRD, RP .
CARCINOGENESIS, 1992, 13 (11) :2081-2085
[35]  
TAHIRA T, 1986, MOL CELL BIOL, V6, P1349, DOI 10.1128/MCB.6.4.1349
[36]  
TAKAYAMA S, 1984, GANN, V75, P467
[37]  
TAKAYAMA S, 1984, JPN J CANCER RES, V75, P207
[38]   KI-RAS ACTIVATION IN PANCREATIC CARCINOMAS OF SYRIAN-HAMSTERS INDUCED BY N-NITROSOBIS(2-HYDROXYPROPYL)AMINE [J].
USHIJIMA, T ;
TSUTSUMI, M ;
SAKAI, R ;
ISHIZAKA, Y ;
TAKAKU, F ;
KONISHI, Y ;
TAKAHASHI, M ;
SUGIMURA, T ;
NAGAO, M .
JAPANESE JOURNAL OF CANCER RESEARCH, 1991, 82 (09) :965-968
[39]  
USHIJIMA T, IN PRESS HETEROCYCLI
[40]   GENETIC ALTERATIONS DURING COLORECTAL-TUMOR DEVELOPMENT [J].
VOGELSTEIN, B ;
FEARON, ER ;
HAMILTON, SR ;
KERN, SE ;
PREISINGER, AC ;
LEPPERT, M ;
NAKAMURA, Y ;
WHITE, R ;
SMITS, AMM ;
BOS, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 319 (09) :525-532