Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography

被引:45
|
作者
Kurzawski, G
Safranow, K
Suchy, J
Chlubek, D
Scott, RJ
Lubinski, J
机构
[1] Pomeranian Acad Med, Dept Genet & Pathol, Hereditary Canc Ctr, PL-70115 Szczecin, Poland
[2] Pomeranian Acad Med, Dept Chem & Biochem, PL-70115 Szczecin, Poland
[3] Univ Newcastle, Discipline Med Genet, Newcastle, NSW 2308, Australia
来源
关键词
DHPLC; MLH1; MSH2; mutation analysis; colorectal cancer; Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC);
D O I
10.1016/S0165-022X(02)00003-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mutation analysis of large genes, such as MSH2 and MLH1, is time-consuming and expensive. We investigated the sensitivity and specificity of DHPLC analysis for the detection of mutations within both MSH2 and MLH1. Studies included a series of 46 patients affected by colorectal cancer from UNPCC families. We confirmed 19 changes previously identified by DNA sequencing and, in a blind study, an additional 16 rare alterations including four mutations not previously described. Generally, false negative results were not observed. Elution profiles were highly characteristic for a given change and in 98.5% cases allowed the distinction between novel alterations and previously identified mutations and polymorphisms. For the detection of changes in almost all amplicons, it was sufficient to use just one denaturing temperature. DHPLC was confirmed to be highly sensitive, specific and a cost-effective technique with particularly high potential for the detection of MSH2 and MLH1 gene mutations in the diagnostic setting. Crown Copyright (C) 2002 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:89 / 100
页数:12
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