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Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma
Although several prognostic signatures have been developed in lung cancer, their application in clinical practice has been limited because they have not been validated in multiple independent data sets. Moreover, the lack of common genes between the signatures makes it difficult to know what biologi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436895/ https://www.ncbi.nlm.nih.gov/pubmed/22970185 http://dx.doi.org/10.1371/journal.pone.0044225 |
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author | Park, Yun-Yong Park, Eun Sung Kim, Sang Bae Kim, Sang Cheol Sohn, Bo Hwa Chu, In-Sun Jeong, Woojin Mills, Gordon B. Byers, Lauren Averett Lee, Ju-Seog |
author_facet | Park, Yun-Yong Park, Eun Sung Kim, Sang Bae Kim, Sang Cheol Sohn, Bo Hwa Chu, In-Sun Jeong, Woojin Mills, Gordon B. Byers, Lauren Averett Lee, Ju-Seog |
author_sort | Park, Yun-Yong |
collection | PubMed |
description | Although several prognostic signatures have been developed in lung cancer, their application in clinical practice has been limited because they have not been validated in multiple independent data sets. Moreover, the lack of common genes between the signatures makes it difficult to know what biological process may be reflected or measured by the signature. By using classical data exploration approach with gene expression data from patients with lung adenocarcinoma (n = 186), we uncovered two distinct subgroups of lung adenocarcinoma and identified prognostic 193-gene gene expression signature associated with two subgroups. The signature was validated in 4 independent lung adenocarcinoma cohorts, including 556 patients. In multivariate analysis, the signature was an independent predictor of overall survival (hazard ratio, 2.4; 95% confidence interval, 1.2 to 4.8; p = 0.01). An integrated analysis of the signature revealed that E2F1 plays key roles in regulating genes in the signature. Subset analysis demonstrated that the gene signature could identify high-risk patients in early stage (stage I disease), and patients who would have benefit of adjuvant chemotherapy. Thus, our study provided evidence for molecular basis of clinically relevant two distinct two subtypes of lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-3436895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34368952012-09-11 Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma Park, Yun-Yong Park, Eun Sung Kim, Sang Bae Kim, Sang Cheol Sohn, Bo Hwa Chu, In-Sun Jeong, Woojin Mills, Gordon B. Byers, Lauren Averett Lee, Ju-Seog PLoS One Research Article Although several prognostic signatures have been developed in lung cancer, their application in clinical practice has been limited because they have not been validated in multiple independent data sets. Moreover, the lack of common genes between the signatures makes it difficult to know what biological process may be reflected or measured by the signature. By using classical data exploration approach with gene expression data from patients with lung adenocarcinoma (n = 186), we uncovered two distinct subgroups of lung adenocarcinoma and identified prognostic 193-gene gene expression signature associated with two subgroups. The signature was validated in 4 independent lung adenocarcinoma cohorts, including 556 patients. In multivariate analysis, the signature was an independent predictor of overall survival (hazard ratio, 2.4; 95% confidence interval, 1.2 to 4.8; p = 0.01). An integrated analysis of the signature revealed that E2F1 plays key roles in regulating genes in the signature. Subset analysis demonstrated that the gene signature could identify high-risk patients in early stage (stage I disease), and patients who would have benefit of adjuvant chemotherapy. Thus, our study provided evidence for molecular basis of clinically relevant two distinct two subtypes of lung adenocarcinoma. Public Library of Science 2012-09-07 /pmc/articles/PMC3436895/ /pubmed/22970185 http://dx.doi.org/10.1371/journal.pone.0044225 Text en © 2012 Park et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Park, Yun-Yong Park, Eun Sung Kim, Sang Bae Kim, Sang Cheol Sohn, Bo Hwa Chu, In-Sun Jeong, Woojin Mills, Gordon B. Byers, Lauren Averett Lee, Ju-Seog Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma |
title | Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma |
title_full | Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma |
title_fullStr | Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma |
title_full_unstemmed | Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma |
title_short | Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma |
title_sort | development and validation of a prognostic gene-expression signature for lung adenocarcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436895/ https://www.ncbi.nlm.nih.gov/pubmed/22970185 http://dx.doi.org/10.1371/journal.pone.0044225 |
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