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Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma
Long non-coding RNAs (lncRNAs) expression profile signature for survival assessment in lung squamous cell carcinoma (LUSC) are largely inconsistent due to distinct detecting approaches and small sample size. Systematic and integrative investigation of RNA-Seq based data from The Cancer Genome Atlas...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584202/ https://www.ncbi.nlm.nih.gov/pubmed/28881601 http://dx.doi.org/10.18632/oncotarget.17098 |
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author | Tang, Rui-Xue Chen, Wen-Jie He, Rong-Quan Zeng, Jiang-Hui Liang, Liang Li, Shi-Kang Ma, Jie Luo, Dian-Zhong Chen, Gang |
author_facet | Tang, Rui-Xue Chen, Wen-Jie He, Rong-Quan Zeng, Jiang-Hui Liang, Liang Li, Shi-Kang Ma, Jie Luo, Dian-Zhong Chen, Gang |
author_sort | Tang, Rui-Xue |
collection | PubMed |
description | Long non-coding RNAs (lncRNAs) expression profile signature for survival assessment in lung squamous cell carcinoma (LUSC) are largely inconsistent due to distinct detecting approaches and small sample size. Systematic and integrative investigation of RNA-Seq based data from The Cancer Genome Atlas (TCGA) herein was performed to determine candidate lncRNAs for prognosis evaluation of LUSC. A total of 60483 genes, including 7589 lncRNAs were assessed in a cohort including 478 LUSC cases with follow-up data. Firstly, 4225 differentially expressed lncRNAs were obtained via R packages. Next, univariate and multivariate Cox proportional hazards regression revealed that 41 lncRNAs were closely related to the survival of LUSC. Finally, lncRNA based prognosis index (PI) could predict overall survival of LUSC with high accuracy (AUC = 0.652, CI: 0.598, 0.705), PI = exp(CYP4F26P)*β(CYP4F26P)+exp(RP11-108M12.3)*β(RP11-108M12.3)+exp(RP11-38M8.1)*β(RP11-38M8.1)+exp(RP11-54H7.4)*β(RP11-54H7.4)+exp(ZNF503-AS1)*β(ZNF503-AS1). Furthermore, it was confirmed that the five-lncRNA signature could act as an independent prognostic indicator for LUSC (HR = 2.068, p < 0.001 with univariate analysis, HR = 1.928, p = 0.038 with multivariate). Besides, we constructed a weighted gene co-expression network analysis (WGCNA) of key lncRNA RP11-54H7.4 according to the p-value of related genes’ weight. This study provides a RNA-Seq based prognostic signature with five lncRNAs for further clinical application to LUSC patients. |
format | Online Article Text |
id | pubmed-5584202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55842022017-09-06 Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma Tang, Rui-Xue Chen, Wen-Jie He, Rong-Quan Zeng, Jiang-Hui Liang, Liang Li, Shi-Kang Ma, Jie Luo, Dian-Zhong Chen, Gang Oncotarget Research Paper Long non-coding RNAs (lncRNAs) expression profile signature for survival assessment in lung squamous cell carcinoma (LUSC) are largely inconsistent due to distinct detecting approaches and small sample size. Systematic and integrative investigation of RNA-Seq based data from The Cancer Genome Atlas (TCGA) herein was performed to determine candidate lncRNAs for prognosis evaluation of LUSC. A total of 60483 genes, including 7589 lncRNAs were assessed in a cohort including 478 LUSC cases with follow-up data. Firstly, 4225 differentially expressed lncRNAs were obtained via R packages. Next, univariate and multivariate Cox proportional hazards regression revealed that 41 lncRNAs were closely related to the survival of LUSC. Finally, lncRNA based prognosis index (PI) could predict overall survival of LUSC with high accuracy (AUC = 0.652, CI: 0.598, 0.705), PI = exp(CYP4F26P)*β(CYP4F26P)+exp(RP11-108M12.3)*β(RP11-108M12.3)+exp(RP11-38M8.1)*β(RP11-38M8.1)+exp(RP11-54H7.4)*β(RP11-54H7.4)+exp(ZNF503-AS1)*β(ZNF503-AS1). Furthermore, it was confirmed that the five-lncRNA signature could act as an independent prognostic indicator for LUSC (HR = 2.068, p < 0.001 with univariate analysis, HR = 1.928, p = 0.038 with multivariate). Besides, we constructed a weighted gene co-expression network analysis (WGCNA) of key lncRNA RP11-54H7.4 according to the p-value of related genes’ weight. This study provides a RNA-Seq based prognostic signature with five lncRNAs for further clinical application to LUSC patients. Impact Journals LLC 2017-04-13 /pmc/articles/PMC5584202/ /pubmed/28881601 http://dx.doi.org/10.18632/oncotarget.17098 Text en Copyright: © 2017 Tang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Tang, Rui-Xue Chen, Wen-Jie He, Rong-Quan Zeng, Jiang-Hui Liang, Liang Li, Shi-Kang Ma, Jie Luo, Dian-Zhong Chen, Gang Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma |
title | Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma |
title_full | Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma |
title_fullStr | Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma |
title_full_unstemmed | Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma |
title_short | Identification of a RNA-Seq based prognostic signature with five lncRNAs for lung squamous cell carcinoma |
title_sort | identification of a rna-seq based prognostic signature with five lncrnas for lung squamous cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584202/ https://www.ncbi.nlm.nih.gov/pubmed/28881601 http://dx.doi.org/10.18632/oncotarget.17098 |
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