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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
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.
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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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