Eintrag weiter verarbeiten
Detection ofEGFRGene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay
Gespeichert in:
Zeitschriftentitel: | Clinical Cancer Research |
---|---|
Personen und Körperschaften: | , , , , , , , , , , , , , , |
In: | Clinical Cancer Research, 12, 2006, 1, S. 43-48 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
American Association for Cancer Research (AACR)
|
Schlagwörter: |
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 |
doi_str_mv |
10.1158/1078-0432.ccr-05-0934 |
facet_avail |
Online Free |
finc_class_facet |
Medizin |
format |
ElectronicArticle |
fullrecord |
blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTE1OC8xMDc4LTA0MzIuY2NyLTA1LTA5MzQ |
id |
ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTE1OC8xMDc4LTA0MzIuY2NyLTA1LTA5MzQ |
institution |
DE-Gla1 DE-Zi4 DE-15 DE-Pl11 DE-Rs1 DE-105 DE-14 DE-Ch1 DE-L229 DE-D275 DE-Bn3 DE-Brt1 DE-D161 DE-Zwi2 |
imprint |
American Association for Cancer Research (AACR), 2006 |
imprint_str_mv |
American Association for Cancer Research (AACR), 2006 |
issn |
1078-0432 1557-3265 |
issn_str_mv |
1078-0432 1557-3265 |
language |
English |
mega_collection |
American Association for Cancer Research (AACR) (CrossRef) |
match_str |
asano2006detectionofegfrgenemutationinlungcancerbymutantenrichedpolymerasechainreactionassay |
publishDateSort |
2006 |
publisher |
American Association for Cancer Research (AACR) |
recordtype |
ai |
record_format |
ai |
series |
Clinical Cancer Research |
source_id |
49 |
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> |
container_issue |
1 |
container_start_page |
43 |
container_title |
Clinical Cancer Research |
container_volume |
12 |
format_de105 |
Article, E-Article |
format_de14 |
Article, E-Article |
format_de15 |
Article, E-Article |
format_de520 |
Article, E-Article |
format_de540 |
Article, E-Article |
format_dech1 |
Article, E-Article |
format_ded117 |
Article, E-Article |
format_degla1 |
E-Article |
format_del152 |
Buch |
format_del189 |
Article, E-Article |
format_dezi4 |
Article |
format_dezwi2 |
Article, E-Article |
format_finc |
Article, E-Article |
format_nrw |
Article, E-Article |
_version_ |
1792347719486930949 |
geogr_code |
not assigned |
last_indexed |
2024-03-01T17:58:14.628Z |
geogr_code_person |
not assigned |
openURL |
url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Detection+ofEGFRGene+Mutation+in+Lung+Cancer+by+Mutant-Enriched+Polymerase+Chain+Reaction+Assay&rft.date=2006-01-01&genre=article&issn=1557-3265&volume=12&issue=1&spage=43&epage=48&pages=43-48&jtitle=Clinical+Cancer+Research&atitle=Detection+of%3Ci%3EEGFR%3C%2Fi%3EGene+Mutation+in+Lung+Cancer+by+Mutant-Enriched+Polymerase+Chain+Reaction+Assay&aulast=Shimizu&aufirst=Nobuyoshi&rft_id=info%3Adoi%2F10.1158%2F1078-0432.ccr-05-0934&rft.language%5B0%5D=eng |
SOLR | |
_version_ | 1792347719486930949 |
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> |
doi_str_mv | 10.1158/1078-0432.ccr-05-0934 |
facet_avail | Online, Free |
finc_class_facet | Medizin |
format | ElectronicArticle |
format_de105 | Article, E-Article |
format_de14 | Article, E-Article |
format_de15 | Article, E-Article |
format_de520 | Article, E-Article |
format_de540 | Article, E-Article |
format_dech1 | Article, E-Article |
format_ded117 | Article, E-Article |
format_degla1 | E-Article |
format_del152 | Buch |
format_del189 | Article, E-Article |
format_dezi4 | Article |
format_dezwi2 | Article, E-Article |
format_finc | Article, E-Article |
format_nrw | Article, E-Article |
geogr_code | not assigned |
geogr_code_person | not assigned |
id | ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTE1OC8xMDc4LTA0MzIuY2NyLTA1LTA5MzQ |
imprint | American Association for Cancer Research (AACR), 2006 |
imprint_str_mv | American Association for Cancer Research (AACR), 2006 |
institution | DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Zwi2 |
issn | 1078-0432, 1557-3265 |
issn_str_mv | 1078-0432, 1557-3265 |
language | English |
last_indexed | 2024-03-01T17:58:14.628Z |
match_str | asano2006detectionofegfrgenemutationinlungcancerbymutantenrichedpolymerasechainreactionassay |
mega_collection | American Association for Cancer Research (AACR) (CrossRef) |
physical | 43-48 |
publishDate | 2006 |
publishDateSort | 2006 |
publisher | American Association for Cancer Research (AACR) |
record_format | ai |
recordtype | ai |
series | Clinical Cancer Research |
source_id | 49 |
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 |