author_facet Asano, Hiroaki
Toyooka, Shinichi
Tokumo, Masaki
Ichimura, Kouichi
Aoe, Keisuke
Ito, Sachio
Tsukuda, Kazunori
Ouchida, Mamoru
Aoe, Motoi
Katayama, Hideki
Hiraki, Akio
Sugi, Kazuro
Kiura, Katsuyuki
Date, Hiroshi
Shimizu, Nobuyoshi
Asano, Hiroaki
Toyooka, Shinichi
Tokumo, Masaki
Ichimura, Kouichi
Aoe, Keisuke
Ito, Sachio
Tsukuda, Kazunori
Ouchida, Mamoru
Aoe, Motoi
Katayama, Hideki
Hiraki, Akio
Sugi, Kazuro
Kiura, Katsuyuki
Date, Hiroshi
Shimizu, Nobuyoshi
author Asano, Hiroaki
Toyooka, Shinichi
Tokumo, Masaki
Ichimura, Kouichi
Aoe, Keisuke
Ito, Sachio
Tsukuda, Kazunori
Ouchida, Mamoru
Aoe, Motoi
Katayama, Hideki
Hiraki, Akio
Sugi, Kazuro
Kiura, Katsuyuki
Date, Hiroshi
Shimizu, Nobuyoshi
spellingShingle Asano, Hiroaki
Toyooka, Shinichi
Tokumo, Masaki
Ichimura, Kouichi
Aoe, Keisuke
Ito, Sachio
Tsukuda, Kazunori
Ouchida, Mamoru
Aoe, Motoi
Katayama, Hideki
Hiraki, Akio
Sugi, Kazuro
Kiura, Katsuyuki
Date, Hiroshi
Shimizu, Nobuyoshi
Clinical Cancer Research
Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
Cancer Research
Oncology
author_sort asano, hiroaki
spelling Asano, Hiroaki Toyooka, Shinichi Tokumo, Masaki Ichimura, Kouichi Aoe, Keisuke Ito, Sachio Tsukuda, Kazunori Ouchida, Mamoru Aoe, Motoi Katayama, Hideki Hiraki, Akio Sugi, Kazuro Kiura, Katsuyuki Date, Hiroshi Shimizu, Nobuyoshi 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-05-0934 <jats:title>Abstract</jats:title><jats:p>Purpose: Mutations in the epidermal growth factor receptor (EGFR) gene have been reported to be present in non–small cell lung cancer (NSCLC) and related to the responsiveness of tumors to EGFR tyrosine kinase inhibitors, suggesting its usefulness as a biomarker. Because clinical samples contain tumor and normal cells or genes, a highly sensitive assay for detecting mutation is critical for clinical applications.</jats:p><jats:p>Experimental Design: The mutant-enriched PCR is a rapid and sensitive assay with selective restriction enzyme digestion. We developed the mutant-enriched PCR assay targeting exons 19 and 21 of EGFR and applied the developed assay to detect mutations in 108 cases of surgically resected specimens of NSCLCs, 18 samples of computed tomography (CT)–guided needle lung biopsies, and 20 samples of pleural fluid. In addition, results were then compared with those from direct sequencing and a nonenriched PCR assay.</jats:p><jats:p>Results: The mutant-enriched PCR that was proved to enrich one mutant of 2 × 103 normal genes detected mutations in 37 cases of 108 resected tumors, seven samples of CT-guided lung biopsies, and seven samples of pleural fluid. Among mutant cases, four resected tumors, two CT-guided lung biopsies, and two pleural fluid were identified as additional mutant cases by the mutant-enriched PCR, which were considered normal based on nonenriched assays.</jats:p><jats:p>Conclusions: Our results indicate that EGFR mutations are readily detectable by mutant-enriched PCR in various clinical samples. Thus, mutant-enriched PCR may provide a valuable method of potentially detecting a small fraction of mutant genes in heterogeneous specimens, indicating its possible use in clinical application for NSCLC.</jats:p> Detection of<i>EGFR</i>Gene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay Clinical Cancer Research
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title Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_unstemmed Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_full Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_fullStr Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_full_unstemmed Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_short Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_sort detection of<i>egfr</i>gene mutation in lung cancer by mutant-enriched polymerase chain reaction assay
topic Cancer Research
Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-05-0934
publishDate 2006
physical 43-48
description <jats:title>Abstract</jats:title><jats:p>Purpose: Mutations in the epidermal growth factor receptor (EGFR) gene have been reported to be present in non–small cell lung cancer (NSCLC) and related to the responsiveness of tumors to EGFR tyrosine kinase inhibitors, suggesting its usefulness as a biomarker. Because clinical samples contain tumor and normal cells or genes, a highly sensitive assay for detecting mutation is critical for clinical applications.</jats:p><jats:p>Experimental Design: The mutant-enriched PCR is a rapid and sensitive assay with selective restriction enzyme digestion. We developed the mutant-enriched PCR assay targeting exons 19 and 21 of EGFR and applied the developed assay to detect mutations in 108 cases of surgically resected specimens of NSCLCs, 18 samples of computed tomography (CT)–guided needle lung biopsies, and 20 samples of pleural fluid. In addition, results were then compared with those from direct sequencing and a nonenriched PCR assay.</jats:p><jats:p>Results: The mutant-enriched PCR that was proved to enrich one mutant of 2 × 103 normal genes detected mutations in 37 cases of 108 resected tumors, seven samples of CT-guided lung biopsies, and seven samples of pleural fluid. Among mutant cases, four resected tumors, two CT-guided lung biopsies, and two pleural fluid were identified as additional mutant cases by the mutant-enriched PCR, which were considered normal based on nonenriched assays.</jats:p><jats:p>Conclusions: Our results indicate that EGFR mutations are readily detectable by mutant-enriched PCR in various clinical samples. Thus, mutant-enriched PCR may provide a valuable method of potentially detecting a small fraction of mutant genes in heterogeneous specimens, indicating its possible use in clinical application for NSCLC.</jats:p>
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author Asano, Hiroaki, Toyooka, Shinichi, Tokumo, Masaki, Ichimura, Kouichi, Aoe, Keisuke, Ito, Sachio, Tsukuda, Kazunori, Ouchida, Mamoru, Aoe, Motoi, Katayama, Hideki, Hiraki, Akio, Sugi, Kazuro, Kiura, Katsuyuki, Date, Hiroshi, Shimizu, Nobuyoshi
author_facet Asano, Hiroaki, Toyooka, Shinichi, Tokumo, Masaki, Ichimura, Kouichi, Aoe, Keisuke, Ito, Sachio, Tsukuda, Kazunori, Ouchida, Mamoru, Aoe, Motoi, Katayama, Hideki, Hiraki, Akio, Sugi, Kazuro, Kiura, Katsuyuki, Date, Hiroshi, Shimizu, Nobuyoshi, Asano, Hiroaki, Toyooka, Shinichi, Tokumo, Masaki, Ichimura, Kouichi, Aoe, Keisuke, Ito, Sachio, Tsukuda, Kazunori, Ouchida, Mamoru, Aoe, Motoi, Katayama, Hideki, Hiraki, Akio, Sugi, Kazuro, Kiura, Katsuyuki, Date, Hiroshi, Shimizu, Nobuyoshi
author_sort asano, hiroaki
container_issue 1
container_start_page 43
container_title Clinical Cancer Research
container_volume 12
description <jats:title>Abstract</jats:title><jats:p>Purpose: Mutations in the epidermal growth factor receptor (EGFR) gene have been reported to be present in non–small cell lung cancer (NSCLC) and related to the responsiveness of tumors to EGFR tyrosine kinase inhibitors, suggesting its usefulness as a biomarker. Because clinical samples contain tumor and normal cells or genes, a highly sensitive assay for detecting mutation is critical for clinical applications.</jats:p><jats:p>Experimental Design: The mutant-enriched PCR is a rapid and sensitive assay with selective restriction enzyme digestion. We developed the mutant-enriched PCR assay targeting exons 19 and 21 of EGFR and applied the developed assay to detect mutations in 108 cases of surgically resected specimens of NSCLCs, 18 samples of computed tomography (CT)–guided needle lung biopsies, and 20 samples of pleural fluid. In addition, results were then compared with those from direct sequencing and a nonenriched PCR assay.</jats:p><jats:p>Results: The mutant-enriched PCR that was proved to enrich one mutant of 2 × 103 normal genes detected mutations in 37 cases of 108 resected tumors, seven samples of CT-guided lung biopsies, and seven samples of pleural fluid. Among mutant cases, four resected tumors, two CT-guided lung biopsies, and two pleural fluid were identified as additional mutant cases by the mutant-enriched PCR, which were considered normal based on nonenriched assays.</jats:p><jats:p>Conclusions: Our results indicate that EGFR mutations are readily detectable by mutant-enriched PCR in various clinical samples. Thus, mutant-enriched PCR may provide a valuable method of potentially detecting a small fraction of mutant genes in heterogeneous specimens, indicating its possible use in clinical application for NSCLC.</jats:p>
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imprint_str_mv American Association for Cancer Research (AACR), 2006
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spelling Asano, Hiroaki Toyooka, Shinichi Tokumo, Masaki Ichimura, Kouichi Aoe, Keisuke Ito, Sachio Tsukuda, Kazunori Ouchida, Mamoru Aoe, Motoi Katayama, Hideki Hiraki, Akio Sugi, Kazuro Kiura, Katsuyuki Date, Hiroshi Shimizu, Nobuyoshi 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-05-0934 <jats:title>Abstract</jats:title><jats:p>Purpose: Mutations in the epidermal growth factor receptor (EGFR) gene have been reported to be present in non–small cell lung cancer (NSCLC) and related to the responsiveness of tumors to EGFR tyrosine kinase inhibitors, suggesting its usefulness as a biomarker. Because clinical samples contain tumor and normal cells or genes, a highly sensitive assay for detecting mutation is critical for clinical applications.</jats:p><jats:p>Experimental Design: The mutant-enriched PCR is a rapid and sensitive assay with selective restriction enzyme digestion. We developed the mutant-enriched PCR assay targeting exons 19 and 21 of EGFR and applied the developed assay to detect mutations in 108 cases of surgically resected specimens of NSCLCs, 18 samples of computed tomography (CT)–guided needle lung biopsies, and 20 samples of pleural fluid. In addition, results were then compared with those from direct sequencing and a nonenriched PCR assay.</jats:p><jats:p>Results: The mutant-enriched PCR that was proved to enrich one mutant of 2 × 103 normal genes detected mutations in 37 cases of 108 resected tumors, seven samples of CT-guided lung biopsies, and seven samples of pleural fluid. Among mutant cases, four resected tumors, two CT-guided lung biopsies, and two pleural fluid were identified as additional mutant cases by the mutant-enriched PCR, which were considered normal based on nonenriched assays.</jats:p><jats:p>Conclusions: Our results indicate that EGFR mutations are readily detectable by mutant-enriched PCR in various clinical samples. Thus, mutant-enriched PCR may provide a valuable method of potentially detecting a small fraction of mutant genes in heterogeneous specimens, indicating its possible use in clinical application for NSCLC.</jats:p> Detection of<i>EGFR</i>Gene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay Clinical Cancer Research
spellingShingle Asano, Hiroaki, Toyooka, Shinichi, Tokumo, Masaki, Ichimura, Kouichi, Aoe, Keisuke, Ito, Sachio, Tsukuda, Kazunori, Ouchida, Mamoru, Aoe, Motoi, Katayama, Hideki, Hiraki, Akio, Sugi, Kazuro, Kiura, Katsuyuki, Date, Hiroshi, Shimizu, Nobuyoshi, Clinical Cancer Research, Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay, Cancer Research, Oncology
title Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_full Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_fullStr Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_full_unstemmed Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_short Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
title_sort detection of<i>egfr</i>gene mutation in lung cancer by mutant-enriched polymerase chain reaction assay
title_unstemmed Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
topic Cancer Research, Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-05-0934