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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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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. |
format | Online Article Text |
id | pubmed-6161724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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