Evaluation of High-Resolution Melting Analysis as a Diagnostic Tool to Detect the BRAF V600E Mutation in Colorectal Tumors

被引:95
作者
Pichler, Martin [1 ]
Balic, Marija [1 ]
Stadelmeyer, Elke [1 ]
Ausch, Christoph [2 ]
Wild, Martina [3 ]
Guelly, Christian [4 ]
Bauemhofer, Thomas [1 ]
Samonigg, Hellmut [1 ]
Hoefler, Gerald [3 ]
Dandachi, Nadia [1 ]
机构
[1] Med Univ Graz, Dept Internal Med, Div Oncol, A-8036 Graz, Austria
[2] Danube Hosp, Ludwig Boltzmann Res Inst Surg Oncol, Dept Surg, Vienna, Austria
[3] Med Univ Graz, Inst Pathol, A-8036 Graz, Austria
[4] Med Univ Graz, Med Res Ctr, A-8036 Graz, Austria
关键词
ISLAND METHYLATOR PHENOTYPE; GROWTH-FACTOR RECEPTOR; ACTIVATING MUTATIONS; SENSITIVE DETECTION; AMPLICON ANALYSIS; COPY NUMBER; C-KIT; KRAS; GENE; CANCER;
D O I
10.2353/jmoldx.2009.080100
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
BRAF V600E is the predominantly occurring mutation of the cytoplasmic kinase BRAF, and, in colorectal cancer, its determination provides a diagnostic exclusion criterion for hereditary nonpolyposis colorectal cancer. The aim of our study was to develop a sensitive BRAF V600E high resolution melting (HRM) assay. We first established and optimized the BRAF HRM assay using a cell tine dilution model, enabling us to detect 1% mutant DNA in a background of wild-type DNA. In a comparison, DNA sequencing and real-time allele-specific PCR in the cell line dilution model HRM assay proved to be more sensitive than DNA sequencing and denaturing high performance liquid chromatography, retaining the same sensitivity as real-time allele-specific PCR. In a learning set of 13 patients with known BRAF V600 status, the mutation was detected with high concordance by all four methods. Finally, we validated the HRM assay on 60 formalin-fixed, paraffm-embedded colorectal cancer samples. Although all mutated samples were correctly identified by HRM, the detection limit of the HRM assay decreased when using low-quality DNA derived from formalin-fixed, paraffin-embedded samples. In conclusion, HRM analysis is a powerful diagnostic tool for detection of BRAF V600E mutation with a high sensitivity and high-throughput capability. Despite the expected decrease in sensitivity, HRM can reliably be applied in archival formalin-fixed, paraffin-embedded samples tissues. (J Mol Diagn 2009, 11:140-147; DOI: 10.2353/jmoldx.2009.080100)
引用
收藏
页码:140 / 147
页数:8
相关论文
共 35 条
[1]
Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer [J].
Amado, Rafael G. ;
Wolf, Michael ;
Peeters, Marc ;
Van Cutsem, Eric ;
Siena, Salvatore ;
Freeman, Daniel J. ;
Juan, Todd ;
Sikorski, Robert ;
Suggs, Sid ;
Radinsky, Robert ;
Patterson, Scott D. ;
Chang, David D. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (10) :1626-1634
[2]
Detection of BRAF V600E mutation in colorectal cancer:: Comparison of automatic sequencing and real-time chemistry methodology [J].
Benlloch, Susana ;
Paya, Artemio ;
Alenda, Cristina ;
Bessa, Xavier ;
Andreu, Montserrat ;
Jover, Rodrigo ;
Castells, Antoni ;
Llor, Xavier ;
Aranda, F. Ignacio ;
Massuti, Bartomeu .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2006, 8 (05) :540-543
[3]
A comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning - Cystic fibrosis transmembrane conductance regulator gene as a model [J].
Chou, LS ;
Lyon, E ;
Wittwer, CT .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2005, 124 (03) :330-338
[4]
Mutations of the BRAF gene in human cancer [J].
Davies, H ;
Bignell, GR ;
Cox, C ;
Stephens, P ;
Edkins, S ;
Clegg, S ;
Teague, J ;
Woffendin, H ;
Garnett, MJ ;
Bottomley, W ;
Davis, N ;
Dicks, N ;
Ewing, R ;
Floyd, Y ;
Gray, K ;
Hall, S ;
Hawes, R ;
Hughes, J ;
Kosmidou, V ;
Menzies, A ;
Mould, C ;
Parker, A ;
Stevens, C ;
Watt, S ;
Hooper, S ;
Wilson, R ;
Jayatilake, H ;
Gusterson, BA ;
Cooper, C ;
Shipley, J ;
Hargrave, D ;
Pritchard-Jones, K ;
Maitland, N ;
Chenevix-Trench, G ;
Riggins, GJ ;
Bigner, DD ;
Palmieri, G ;
Cossu, A ;
Flanagan, A ;
Nicholson, A ;
Ho, JWC ;
Leung, SY ;
Yuen, ST ;
Weber, BL ;
Siegler, HF ;
Darrow, TL ;
Paterson, H ;
Marais, R ;
Marshall, CJ ;
Wooster, R .
NATURE, 2002, 417 (6892) :949-954
[5]
High resolution melting analysis for rapid and sensitive EGFR and KRAS mutation detection in formalin fixed paraffin embedded biopsies [J].
Do, Hongdo ;
Krypuy, Michael ;
Mitchell, Paul L. ;
Fox, Stephen B. ;
Dobrovic, Alexander .
BMC CANCER, 2008, 8 (1)
[6]
RRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes [J].
Domingo, E ;
Niessen, RC ;
Oliveira, C ;
Alhopuro, P ;
Moutinho, C ;
Espín, E ;
Armengol, M ;
Sijmons, RH ;
Kleibeuker, JH ;
Seruca, R ;
Aaltonen, LA ;
Imai, K ;
Yamamoto, H ;
Schwartz, S ;
Hofstra, RMW .
ONCOGENE, 2005, 24 (24) :3995-3998
[7]
BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing [J].
Domingo, E ;
Laiho, P ;
Ollikainen, M ;
Pinto, M ;
Wang, L ;
French, AJ ;
Westra, J ;
Frebourg, T ;
Espín, E ;
Armengol, M ;
Hamelin, R ;
Yamamoto, H ;
Hofstra, RMW ;
Seruca, R ;
Lindblom, A ;
Peltomäki, P ;
Thibodeau, SN ;
Aaltonen, LA ;
Schwartz, S .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (09) :664-668
[8]
High-resolution melting amplicon analysis as a method to detect c-kit and platelet-derived growth factor receptor α activating mutations in gastrointestinal stromal tumors [J].
Holden, Joseph A. ;
Willmore-Payne, Carlynn ;
Coppola, Domenico ;
Garrett, Christopher R. ;
Layfield, Lester J. .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2007, 128 (02) :230-238
[9]
BRAF mutation associated with dysregulation of apoptosis in human colorectal neoplasms [J].
Ikehara, N ;
Semba, S ;
Sakashita, M ;
Aoyama, N ;
Kasuga, M ;
Yokozaki, H .
INTERNATIONAL JOURNAL OF CANCER, 2005, 115 (06) :943-950
[10]
Real-time allele-specific amplification for sensitive detection of the BRAF mutation V600E [J].
Jarry, A ;
Masson, D ;
Cassagnau, E ;
Parois, S ;
Laboisse, C ;
Denis, MG .
MOLECULAR AND CELLULAR PROBES, 2004, 18 (05) :349-352