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Molecular gene signature and prognosis of non-small cell lung cancer
The current staging system for non–small cell lung cancer (NSCLC) is inadequate for predicting outcome. Risk score, a linear combination of the values for the expression of each gene multiplied by a weighting value which was estimated from univariate Cox proportional hazard regression, can be useful...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239522/ https://www.ncbi.nlm.nih.gov/pubmed/27437769 http://dx.doi.org/10.18632/oncotarget.10622 |
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author | Huang, Poyin Cheng, Chiou-Ling Chang, Ya-Hsuan Liu, Chia-Hsin Hsu, Yi-Chiung Chen, Jin-Shing Chang, Gee-Chen Ho, Bing-Ching Su, Kang-Yi Chen, Hsuan-Yu Yu, Sung-Liang |
author_facet | Huang, Poyin Cheng, Chiou-Ling Chang, Ya-Hsuan Liu, Chia-Hsin Hsu, Yi-Chiung Chen, Jin-Shing Chang, Gee-Chen Ho, Bing-Ching Su, Kang-Yi Chen, Hsuan-Yu Yu, Sung-Liang |
author_sort | Huang, Poyin |
collection | PubMed |
description | The current staging system for non–small cell lung cancer (NSCLC) is inadequate for predicting outcome. Risk score, a linear combination of the values for the expression of each gene multiplied by a weighting value which was estimated from univariate Cox proportional hazard regression, can be useful. The aim of this study is to analyze survival-related genes with TaqMan Low-Density Array (TLDA) and risk score to explore gene-signature in lung cancer. A total of 96 NSCLC specimens were collected and randomly assigned to a training (n = 48) or a testing cohort (n = 48). A panel of 219 survival-associated genes from published studies were used to develop a 6-gene risk score. The risk score was used to classify patients into high or low-risk signature and survival analysis was performed. Cox models were used to evaluate independent prognostic factors. A 6-gene signature including ABCC4, ADRBK2, KLHL23, PDS5A, UHRF1 and ZNF551 was identified. The risk score in both training (HR = 3.14, 95% CI: 1.14–8.67, p = 0.03) and testing cohorts (HR = 5.42, 95% CI: 1.56–18.84, p = 0.01) was the independent prognostic factor. In merged public datasets including GSE50081, GSE30219, GSE31210, GSE19188, GSE37745, GSE3141 and GSE31908, the risk score (HR = 1.50, 95% CI: 1.25–1.80, p < 0.0001) was also the independent prognostic factor. The risk score generated from expression of a small number of genes did perform well in predicting overall survival and may be useful in routine clinical practice. |
format | Online Article Text |
id | pubmed-5239522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52395222017-01-24 Molecular gene signature and prognosis of non-small cell lung cancer Huang, Poyin Cheng, Chiou-Ling Chang, Ya-Hsuan Liu, Chia-Hsin Hsu, Yi-Chiung Chen, Jin-Shing Chang, Gee-Chen Ho, Bing-Ching Su, Kang-Yi Chen, Hsuan-Yu Yu, Sung-Liang Oncotarget Research Paper The current staging system for non–small cell lung cancer (NSCLC) is inadequate for predicting outcome. Risk score, a linear combination of the values for the expression of each gene multiplied by a weighting value which was estimated from univariate Cox proportional hazard regression, can be useful. The aim of this study is to analyze survival-related genes with TaqMan Low-Density Array (TLDA) and risk score to explore gene-signature in lung cancer. A total of 96 NSCLC specimens were collected and randomly assigned to a training (n = 48) or a testing cohort (n = 48). A panel of 219 survival-associated genes from published studies were used to develop a 6-gene risk score. The risk score was used to classify patients into high or low-risk signature and survival analysis was performed. Cox models were used to evaluate independent prognostic factors. A 6-gene signature including ABCC4, ADRBK2, KLHL23, PDS5A, UHRF1 and ZNF551 was identified. The risk score in both training (HR = 3.14, 95% CI: 1.14–8.67, p = 0.03) and testing cohorts (HR = 5.42, 95% CI: 1.56–18.84, p = 0.01) was the independent prognostic factor. In merged public datasets including GSE50081, GSE30219, GSE31210, GSE19188, GSE37745, GSE3141 and GSE31908, the risk score (HR = 1.50, 95% CI: 1.25–1.80, p < 0.0001) was also the independent prognostic factor. The risk score generated from expression of a small number of genes did perform well in predicting overall survival and may be useful in routine clinical practice. Impact Journals LLC 2016-07-16 /pmc/articles/PMC5239522/ /pubmed/27437769 http://dx.doi.org/10.18632/oncotarget.10622 Text en Copyright: © 2016 Huang et al. http://creativecommons.org/licenses/by/2.5/ 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 credited. |
spellingShingle | Research Paper Huang, Poyin Cheng, Chiou-Ling Chang, Ya-Hsuan Liu, Chia-Hsin Hsu, Yi-Chiung Chen, Jin-Shing Chang, Gee-Chen Ho, Bing-Ching Su, Kang-Yi Chen, Hsuan-Yu Yu, Sung-Liang Molecular gene signature and prognosis of non-small cell lung cancer |
title | Molecular gene signature and prognosis of non-small cell lung cancer |
title_full | Molecular gene signature and prognosis of non-small cell lung cancer |
title_fullStr | Molecular gene signature and prognosis of non-small cell lung cancer |
title_full_unstemmed | Molecular gene signature and prognosis of non-small cell lung cancer |
title_short | Molecular gene signature and prognosis of non-small cell lung cancer |
title_sort | molecular gene signature and prognosis of non-small cell lung cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239522/ https://www.ncbi.nlm.nih.gov/pubmed/27437769 http://dx.doi.org/10.18632/oncotarget.10622 |
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