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An expression signature model to predict lung adenocarcinoma-specific survival

BACKGROUND: The current TNM staging system plays a central role in lung adenocarcinoma (LUAD) prognosis. However, it may not adequately stratify the risk of tumor recurrence. With the aid of gene expression profiling, we identified 31 lncRNAs whose expressions in tumor tissues could be used as a ris...

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Autores principales: Shi, Xiaoshun, Tan, Haoming, Le, Xiaobing, Xian, Haibing, Li, Xiaoxiang, Huang, Kailing, Luo, Viola Yingjun, Liu, Yanhui, Wu, Zhuolin, Mo, Haiyun, Chen, Allen M, Liang, Ying, Zhang, Jiexia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161724/
https://www.ncbi.nlm.nih.gov/pubmed/30288103
http://dx.doi.org/10.2147/CMAR.S159563
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author Shi, Xiaoshun
Tan, Haoming
Le, Xiaobing
Xian, Haibing
Li, Xiaoxiang
Huang, Kailing
Luo, Viola Yingjun
Liu, Yanhui
Wu, Zhuolin
Mo, Haiyun
Chen, Allen M
Liang, Ying
Zhang, Jiexia
author_facet Shi, Xiaoshun
Tan, Haoming
Le, Xiaobing
Xian, Haibing
Li, Xiaoxiang
Huang, Kailing
Luo, Viola Yingjun
Liu, Yanhui
Wu, Zhuolin
Mo, Haiyun
Chen, Allen M
Liang, Ying
Zhang, Jiexia
author_sort Shi, Xiaoshun
collection PubMed
description BACKGROUND: The current TNM staging system plays a central role in lung adenocarcinoma (LUAD) prognosis. However, it may not adequately stratify the risk of tumor recurrence. With the aid of gene expression profiling, we identified 31 lncRNAs whose expressions in tumor tissues could be used as a risk indicator for the guidance of lung cancer therapy. This exploratory analysis may shed new light on identification of potential prognostic factors. MATERIALS AND METHODS: A survival prediction scoring model was developed from the data that are publicly available in The Cancer Genome Atlas (TCGA) LUAD RNA Sequencing dataset. Multivariate Cox regression analysis and Kaplan–Meier analysis were performed on a cohort of 254 stage I lung carcinoma patients with survival records. RESULTS: Our model indicates that the panels comprising 31 lncRNAs are highly associated with overall survival (OS): 18.9% (95% CI: 10.4%–34.5%) and 89.5% (95% CI: 80.7%–99.2%) for the high- and low-risk group, respectively. The specificity and sensitivity of the model are verified, which show that the area under receiver operating characteristic curve yields 0.881, meaning our model has good accuracy and it is feasible for further applications. CONCLUSION: The 31-lncRNA model might be able to predict OS in patients with LUAD with high accuracy. Its further applications in biomolecular experiments using clinical samples with independent cohorts of patients are needed to verify the results.
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spelling pubmed-61617242018-10-04 An expression signature model to predict lung adenocarcinoma-specific survival Shi, Xiaoshun Tan, Haoming Le, Xiaobing Xian, Haibing Li, Xiaoxiang Huang, Kailing Luo, Viola Yingjun Liu, Yanhui Wu, Zhuolin Mo, Haiyun Chen, Allen M Liang, Ying Zhang, Jiexia Cancer Manag Res Original Research BACKGROUND: The current TNM staging system plays a central role in lung adenocarcinoma (LUAD) prognosis. However, it may not adequately stratify the risk of tumor recurrence. With the aid of gene expression profiling, we identified 31 lncRNAs whose expressions in tumor tissues could be used as a risk indicator for the guidance of lung cancer therapy. This exploratory analysis may shed new light on identification of potential prognostic factors. MATERIALS AND METHODS: A survival prediction scoring model was developed from the data that are publicly available in The Cancer Genome Atlas (TCGA) LUAD RNA Sequencing dataset. Multivariate Cox regression analysis and Kaplan–Meier analysis were performed on a cohort of 254 stage I lung carcinoma patients with survival records. RESULTS: Our model indicates that the panels comprising 31 lncRNAs are highly associated with overall survival (OS): 18.9% (95% CI: 10.4%–34.5%) and 89.5% (95% CI: 80.7%–99.2%) for the high- and low-risk group, respectively. The specificity and sensitivity of the model are verified, which show that the area under receiver operating characteristic curve yields 0.881, meaning our model has good accuracy and it is feasible for further applications. CONCLUSION: The 31-lncRNA model might be able to predict OS in patients with LUAD with high accuracy. Its further applications in biomolecular experiments using clinical samples with independent cohorts of patients are needed to verify the results. Dove Medical Press 2018-09-24 /pmc/articles/PMC6161724/ /pubmed/30288103 http://dx.doi.org/10.2147/CMAR.S159563 Text en © 2018 Shi et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Shi, Xiaoshun
Tan, Haoming
Le, Xiaobing
Xian, Haibing
Li, Xiaoxiang
Huang, Kailing
Luo, Viola Yingjun
Liu, Yanhui
Wu, Zhuolin
Mo, Haiyun
Chen, Allen M
Liang, Ying
Zhang, Jiexia
An expression signature model to predict lung adenocarcinoma-specific survival
title An expression signature model to predict lung adenocarcinoma-specific survival
title_full An expression signature model to predict lung adenocarcinoma-specific survival
title_fullStr An expression signature model to predict lung adenocarcinoma-specific survival
title_full_unstemmed An expression signature model to predict lung adenocarcinoma-specific survival
title_short An expression signature model to predict lung adenocarcinoma-specific survival
title_sort expression signature model to predict lung adenocarcinoma-specific survival
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161724/
https://www.ncbi.nlm.nih.gov/pubmed/30288103
http://dx.doi.org/10.2147/CMAR.S159563
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