Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing

Due to the call for fast KRAS mutation status analysis for treatment of patients with monoclonal antibodies for metastatic colorectal cancer, sensitive, economic, and easily feasible methods are required. Under this aspect, the sensitivity and specificity of the SNaPshot analysis in comparison to th...

Full description

Saved in:
Bibliographic Details
Main Authors: Rica Zinsky, Servet Bölükbas, Holger Bartsch, Joachim Schirren, Annette Fisseler-Eckhoff
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Gastroenterology Research and Practice
Online Access:http://dx.doi.org/10.1155/2010/789363
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832548136388657152
author Rica Zinsky
Servet Bölükbas
Holger Bartsch
Joachim Schirren
Annette Fisseler-Eckhoff
author_facet Rica Zinsky
Servet Bölükbas
Holger Bartsch
Joachim Schirren
Annette Fisseler-Eckhoff
author_sort Rica Zinsky
collection DOAJ
description Due to the call for fast KRAS mutation status analysis for treatment of patients with monoclonal antibodies for metastatic colorectal cancer, sensitive, economic, and easily feasible methods are required. Under this aspect, the sensitivity and specificity of the SNaPshot analysis in comparison to the commonly used DNA sequencing was checked. We examined KRAS mutations in exon 2 codons 12 and 13 with DNA sequencing and SNaPshot analysis in 100 formalin-fixed paraffin-embedded tumor tissue samples of pancreatic carcinoma, colorectal carcinoma, and nonsmall cell lung cancer specimens of the primary tumor or metastases. 40% of these samples demonstrated mutated KRAS genes using sequencing and SNaPshot-analysis; additional five samples (45/100) were identified only with the SNaPshot. KRAS mutation detection is feasible with the reliable SNaPshot analysis method. The more frequent mutation detection by the SNaPshot analysis shows that this method has a high probability of accuracy in the detection of KRAS mutations compared to sequencing.
format Article
id doaj-art-9fcd561ce8db4e489bd1b706bb8f69c5
institution Kabale University
issn 1687-6121
1687-630X
language English
publishDate 2010-01-01
publisher Wiley
record_format Article
series Gastroenterology Research and Practice
spelling doaj-art-9fcd561ce8db4e489bd1b706bb8f69c52025-02-03T06:42:08ZengWileyGastroenterology Research and Practice1687-61211687-630X2010-01-01201010.1155/2010/789363789363Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA SequencingRica Zinsky0Servet Bölükbas1Holger Bartsch2Joachim Schirren3Annette Fisseler-Eckhoff4Institute of Pathology and Cytology, HSK Wiesbaden, Academic Hospital of University of Mainz, Ludwig-Erhard-Strasse 100, 65199 Wiesbaden, GermanyDepartment of Thoracic Surgery, HSK Wiesbaden, Academic Hospital of University of Mainz, Ludwig-Erhard-Strasse 100, 65199 Wiesbaden, GermanyInstitute of Pathology and Cytology, HSK Wiesbaden, Academic Hospital of University of Mainz, Ludwig-Erhard-Strasse 100, 65199 Wiesbaden, GermanyDepartment of Thoracic Surgery, HSK Wiesbaden, Academic Hospital of University of Mainz, Ludwig-Erhard-Strasse 100, 65199 Wiesbaden, GermanyInstitute of Pathology and Cytology, HSK Wiesbaden, Academic Hospital of University of Mainz, Ludwig-Erhard-Strasse 100, 65199 Wiesbaden, GermanyDue to the call for fast KRAS mutation status analysis for treatment of patients with monoclonal antibodies for metastatic colorectal cancer, sensitive, economic, and easily feasible methods are required. Under this aspect, the sensitivity and specificity of the SNaPshot analysis in comparison to the commonly used DNA sequencing was checked. We examined KRAS mutations in exon 2 codons 12 and 13 with DNA sequencing and SNaPshot analysis in 100 formalin-fixed paraffin-embedded tumor tissue samples of pancreatic carcinoma, colorectal carcinoma, and nonsmall cell lung cancer specimens of the primary tumor or metastases. 40% of these samples demonstrated mutated KRAS genes using sequencing and SNaPshot-analysis; additional five samples (45/100) were identified only with the SNaPshot. KRAS mutation detection is feasible with the reliable SNaPshot analysis method. The more frequent mutation detection by the SNaPshot analysis shows that this method has a high probability of accuracy in the detection of KRAS mutations compared to sequencing.http://dx.doi.org/10.1155/2010/789363
spellingShingle Rica Zinsky
Servet Bölükbas
Holger Bartsch
Joachim Schirren
Annette Fisseler-Eckhoff
Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing
Gastroenterology Research and Practice
title Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing
title_full Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing
title_fullStr Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing
title_full_unstemmed Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing
title_short Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing
title_sort analysis of kras mutations of exon 2 codons 12 and 13 by snapshot analysis in comparison to common dna sequencing
url http://dx.doi.org/10.1155/2010/789363
work_keys_str_mv AT ricazinsky analysisofkrasmutationsofexon2codons12and13bysnapshotanalysisincomparisontocommondnasequencing
AT servetbolukbas analysisofkrasmutationsofexon2codons12and13bysnapshotanalysisincomparisontocommondnasequencing
AT holgerbartsch analysisofkrasmutationsofexon2codons12and13bysnapshotanalysisincomparisontocommondnasequencing
AT joachimschirren analysisofkrasmutationsofexon2codons12and13bysnapshotanalysisincomparisontocommondnasequencing
AT annettefisselereckhoff analysisofkrasmutationsofexon2codons12and13bysnapshotanalysisincomparisontocommondnasequencing