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A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma
Glioblastoma (GBM) is an aggressive tumor of the central nervous system that has poor prognosis despite extensive therapy. Therefore, it is essential to identify a gene expression-based signature for predicting GBM prognosis. The RNA sequencing data of GBM patients from the Chinese Glioma Genome Atl...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385312/ https://www.ncbi.nlm.nih.gov/pubmed/30796273 http://dx.doi.org/10.1038/s41598-019-39273-4 |
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author | Zuo, Shuguang Zhang, Xinhong Wang, Liping |
author_facet | Zuo, Shuguang Zhang, Xinhong Wang, Liping |
author_sort | Zuo, Shuguang |
collection | PubMed |
description | Glioblastoma (GBM) is an aggressive tumor of the central nervous system that has poor prognosis despite extensive therapy. Therefore, it is essential to identify a gene expression-based signature for predicting GBM prognosis. The RNA sequencing data of GBM patients from the Chinese Glioma Genome Atlas (CGGA) and The Cancer Genome Atlas (TCGA) databases were employed in our study. The univariate and multivariate regression models were utilized to assess the relative contribution of each gene to survival prediction in both cohorts, and the common genes in two cohorts were identified as a final prognostic model. A prognostic risk score was calculated based on the prognostic gene signature. This prognostic signature stratified the patients into the low- and high-risk groups. Multivariate regression and stratification analyses were implemented to determine whether the gene signature was an independent prognostic factor. We identified a 6-gene signature through univariate and multivariate regression models. This prognostic signature stratified the patients into the low- and high-risk groups, implying improved and poor outcomes respectively. Multivariate regression and stratification analyses demonstrated that the predictive value of the 6-gene signature was independent of other clinical factors. This study highlights the significant implications of having a gene signature as a prognostic predictor in GBM, and its potential application in personalized therapy. |
format | Online Article Text |
id | pubmed-6385312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63853122019-02-27 A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma Zuo, Shuguang Zhang, Xinhong Wang, Liping Sci Rep Article Glioblastoma (GBM) is an aggressive tumor of the central nervous system that has poor prognosis despite extensive therapy. Therefore, it is essential to identify a gene expression-based signature for predicting GBM prognosis. The RNA sequencing data of GBM patients from the Chinese Glioma Genome Atlas (CGGA) and The Cancer Genome Atlas (TCGA) databases were employed in our study. The univariate and multivariate regression models were utilized to assess the relative contribution of each gene to survival prediction in both cohorts, and the common genes in two cohorts were identified as a final prognostic model. A prognostic risk score was calculated based on the prognostic gene signature. This prognostic signature stratified the patients into the low- and high-risk groups. Multivariate regression and stratification analyses were implemented to determine whether the gene signature was an independent prognostic factor. We identified a 6-gene signature through univariate and multivariate regression models. This prognostic signature stratified the patients into the low- and high-risk groups, implying improved and poor outcomes respectively. Multivariate regression and stratification analyses demonstrated that the predictive value of the 6-gene signature was independent of other clinical factors. This study highlights the significant implications of having a gene signature as a prognostic predictor in GBM, and its potential application in personalized therapy. Nature Publishing Group UK 2019-02-22 /pmc/articles/PMC6385312/ /pubmed/30796273 http://dx.doi.org/10.1038/s41598-019-39273-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zuo, Shuguang Zhang, Xinhong Wang, Liping A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma |
title | A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma |
title_full | A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma |
title_fullStr | A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma |
title_full_unstemmed | A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma |
title_short | A RNA sequencing-based six-gene signature for survival prediction in patients with glioblastoma |
title_sort | rna sequencing-based six-gene signature for survival prediction in patients with glioblastoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385312/ https://www.ncbi.nlm.nih.gov/pubmed/30796273 http://dx.doi.org/10.1038/s41598-019-39273-4 |
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