Early detection of 2-amino-1-methyl-6-phenylimidazo (4,5-b)pyridine(PhIP)-induced mutations within the Apc gene of rat colon

被引:14
|
作者
Burnouf, DY
Miturski, R
Nagao, M
Nakagama, H
Nothisen, M
Wagner, J
Fuchs, RPP
机构
[1] Inst Rech Canc Appareil Digestif, CNRS, UPR 9003, Grp Epidemiol Mol Canc, F-67097 Strasbourg, France
[2] Natl Canc Ctr, Res Inst, Chuo Ku, Tokyo 1040045, Japan
关键词
D O I
10.1093/carcin/22.2.329
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A large proportion of human cancers result from exposure of individuals to environmental or occupational carcinogens. The early detection of carcinogen-induced mutations is a prerequisite for the identification of individuals at risk for developing cancer. Short G-rich repetitive sequences have been previously identified as hot-spots for frameshift mutagenesis induced by a large variety of carcinogens belonging to several families of widespread environmental pollutants, In order to test if these sequences, when mutated, might serve as biomarkers for carcinogen exposure, we designed a sensitive PCR-based strategy that allows the detection of rare mutational events within a whole genome, 2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP), the most abundant carcinogenic heterocyclic amine generated in cooked meat, induces mammary and colon carcinoma in F344 rats. About 25% of male rats exposed to 400 p.p.m. PhIP in the diet for >43 weeks present colon tumors with specific -1G mutations within 5'-GGGA-3' sequences of the Ape gene. Using our PCR assay we have assessed the occurrence of such specific events in rats exposed to PhIP for only 1, 2, 4 and 6 weeks. A specific amplification signal was already observed in the 1 week-treated population and increases in a treatment time-dependent manner. These data validate this approach for the early detection of mutations and demonstrate its usefulness for molecular epidemiology and early diagnosis.
引用
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页码:329 / 335
页数:7
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