MUTATIONAL ANALYSIS OF A DOMINANT ONCOGENE (C-KI-RAS-2) AND A TUMOR SUPPRESSOR GENE (P53) IN HAMSTER LUNG TUMORIGENESIS

被引:24
作者
OREFFO, VIC
LIN, HW
GUMERLOCK, PH
KRAEGEL, SA
WITSCHI, H
机构
[1] UNIV CALIF DAVIS,TOX SUBSTANCES RES & TEACHING PROGRAM,DAVIS,CA 95616
[2] UNIV CALIF DAVIS,DEPT INTERNAL MED,DIV PULM CRIT CARE MED,DAVIS,CA 95616
[3] UNIV CALIF DAVIS,SCH VET MED,DEPT SURG,DAVIS,CA 95616
关键词
LUNG CANCER; ONCOGENE ACTIVATION; POLYMERASE CHAIN REACTION; KI-RAS; P53; SYRIAN GOLDEN HAMSTER;
D O I
10.1002/mc.2940060305
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
In human lung cancers, alterations of both a dominant oncogene (ras) and a tumor suppressor gene (p53) have been identified. Polymerase chain reaction (PCR) analysis of mRNA was used to amplify the c-Ki-ras-2 and p53 genes from Syrian golden hamsters. The PCR products were confirmed by predicted-size analysis, probing with nonradioactive (biotin-labeled) oligonucleotides, and direct sequencing. Lung tumors were produced in hamsters by repeated injections of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK). Of six tumors examined, three (50%) had mutations in codon 12 of Ki-ras. Examination of the conserved regions of p53 revealed no mutations. We conclude that NNK-induced carcinogenesis in the hamster results in characteristic alterations of Ki-ras but may not necessarily involve the p53 gene.
引用
收藏
页码:199 / 202
页数:4
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