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
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2002年 / 51卷 / 01期
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
相关论文
共 50 条
  • [21] Expression of MLH1 and MSH2 in urothelial carcinoma of the renal pelvis
    Ehsani, Laleh
    Osunkoya, Adeboye O.
    TUMOR BIOLOGY, 2014, 35 (09) : 8743 - 8747
  • [22] Spectrum of MLH1 and MSH2 Mutations in Chilean Families With Suspected Lynch Syndrome
    Alvarez, Karin
    Hurtado, Claudia
    Hevia, Montserrat A.
    Wielandt, Ana Maria
    de la Fuente, Marjorie
    Church, James
    Carvallo, Pilar
    Lopez-Koestner, Francisco
    DISEASES OF THE COLON & RECTUM, 2010, 53 (04) : 450 - 459
  • [23] A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1
    Wang, YP
    Friedl, W
    Sengteller, M
    Jungck, M
    Filges, I
    Propping, P
    Mangold, E
    HUMAN MUTATION, 2002, 19 (03) : 279 - 286
  • [24] RACIAL DIFFERENCES IN MLH1 AND MSH2 MUTATION: AN ANALYSIS OF YELLOW RACE AND WHITE RACE BASED ON THE INSIGHT DATABASE
    Wei, Wenqian
    Liu, Lei
    Chen, Jian
    Jin, Ke
    Jiang, Fan
    Liu, Fangqi
    Fan, Rong
    Cheng, Zhe
    Shen, Meng
    Xue, Chenyi
    Cai, Sanjun
    Xu, Ye
    Nan, Peng
    JOURNAL OF BIOINFORMATICS AND COMPUTATIONAL BIOLOGY, 2010, 8 : 111 - 125
  • [25] First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome
    Ziada-Bouchaar, H.
    Sifi, K.
    Filali, T.
    Hammada, T.
    Satta, D.
    Abadi, N.
    FAMILIAL CANCER, 2017, 16 (01) : 57 - 66
  • [26] The role of MLH1, MSH2 and MSH6 in the development of colorectal cancer in Uganda
    Richard Wismayer
    Rosie Matthews
    Celina Whalley
    Julius Kiwanuka
    Fredrick Elishama Kakembo
    Steve Thorn
    Henry Wabinga
    Michael Odida
    Ian Tomlinson
    BMC Cancer, 25 (1)
  • [27] Missense Mutations in MLH1, MSH2, KRAS, and APC Genes in Colorectal Cancer Patients in Malaysia
    Nor Azian Abdul Murad
    Zulhabri Othman
    Melati Khalid
    Zuraini Abdul Razak
    Rosniza Hussain
    Sukumar Nadesan
    Ismail Sagap
    Isa Mohamed Rose
    Wan Zurinah Wan Ngah
    Rahman Jamal
    Digestive Diseases and Sciences, 2012, 57 : 2863 - 2872
  • [28] Genetic changes of MLH1 and MSH2 genes could explain constant findings on microsatellite instability in intracranial meningioma
    Pecina-Slaus, Nives
    Kafka, Anja
    Bukovac, Anja
    Vladusic, Tomislav
    Tomas, Davor
    Hrascan, Reno
    TUMOR BIOLOGY, 2017, 39 (07)
  • [29] Single nucleotide polymorphisms of DNA mismatch repair genes MSH2 and MLH1 confer susceptibility to esophageal cancer
    Sun, Ming-Zhong
    Ju, Hui-Xiang
    Zhou, Zhong-Wei
    Jin, Hao
    Zhu, Rong
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2014, 7 (08): : 2329 - 2333
  • [30] Assessing How Reduced Expression Levels of the Mismatch Repair Genes MLH1, MSH2, and MSH6 Affect Repair Efficiency
    Kansikas, Minttu
    Kasela, Mariann
    Kantelinen, Jukka
    Nystrom, Minna
    HUMAN MUTATION, 2014, 35 (09) : 1123 - 1127