K-ras and p53 mutations in hereditary non-polyposis colorectal cancers

被引:0
|
作者
Losi, L
DeLeon, MP
Jiricny, J
DiGregorio, C
Benatti, P
Percesepe, A
Fante, R
Roncucci, L
Pedroni, M
Benhattar, J
机构
[1] UNIV LAUSANNE,INST PATHOL,CH-1011 LAUSANNE,SWITZERLAND
[2] UNIV MODENA,INST ANAT,I-41100 MODENA,ITALY
[3] UNIV MODENA,INST PATHOL HISTOL,COLORECTAL CANC STUDY GRP,I-41100 MODENA,ITALY
[4] IRBM,I-00040 POMEZIA,ITALY
[5] RAMAZZINI HOSP,SERV ANAT PATHOL,CARPI,ITALY
[6] HLTH CARE DIST 16,MODENA,ITALY
关键词
D O I
10.1002/(SICI)1097-0215(19970220)74:1<94::AID-IJC16>3.0.CO;2-I
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetic instability related to defective DNA mismatch repair genes may be involved in the pathogenesis of carcinoma in Hereditary Non-Polyposis Colorectal Cancer (HNPCC). To test that the targets of genetic instability could include critical transforming genes involved in colon tumor progression, we examined 23 colorectal carcinomas in patients with HNPCC in order to detect somatic mutations in K-ros and p53 genes. Using single strand conformation polymorphism followed by direct DNA sequencing, we detected 4 mutations in K-ros gene (17%) and 3 in p53 gene (13%) which change the aminoacid sequence of the protein p53. This is significantly lower than in sporadic cancer. Our data suggest that colon cancer in HNPCC might partly involve a distinct pathogenetic mechanism that involves other genes than those altered in sporadic tumors. (C) 1997 Wiley-Liss, Inc,.
引用
收藏
页码:94 / 96
页数:3
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