Somatic β-catenin mutation in gastric carcinoma -: an infrequent event that is not specific for microsatellite instability

被引:25
作者
Tong, JHM
To, KF [1 ]
Ng, EKW
Lau, JYW
Lee, TL
Lo, KW
Leung, WK
Tang, NLS
Chan, FKL
Sung, JJY
Chung, SCS
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Anat & Cellular Pathol, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Surg, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Chem Pathol, Hong Kong, Hong Kong, Peoples R China
关键词
gastric carcinoma; beta-Catenin; microsatellite instability;
D O I
10.1016/S0304-3835(00)00681-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We screened 90 cases of gastric carcinoma (GCA) samples for beta -catenin exon 3 mutation and assessed its possible relationship with microsatellite instability (MSI). Three mutations were detected in two samples, including a single mutation in an intestinal type and double mutations in a diffuse type GCA. One of the mutations found in the diffuse type GCA sample was a non-sense mutation at codon 68 (CAG --> TAG). This novel mutation was predicted to disrupt the binding of beta -catenin to alpha -catenin and may be related to the diffuse type morphology. The other two mutations were missense mutations involved or related to the GSK-3 beta phosphorylation site, which have been reported previously. No MSI can be demonstrated in the two cases with beta -catenin mutation. Our results suggested that beta -catenin mutation was infrequent in GCA and appeared not specific for MSI. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:125 / 130
页数:6
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