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Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis
Emerging evidence suggests that alternative splicing (AS) is modified in cancer and is associated with cancer progression. Systematic analysis of AS signature in glioblastoma (GBM) is lacking and is greatly needed. We profiled genome-wide AS events in 498 GBM patients in TCGA using RNA-seq data, and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769083/ https://www.ncbi.nlm.nih.gov/pubmed/31608231 http://dx.doi.org/10.3389/fonc.2019.00928 |
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author | Chen, Xueran Zhao, Chenggang Guo, Bing Zhao, Zhiyang Wang, Hongzhi Fang, Zhiyou |
author_facet | Chen, Xueran Zhao, Chenggang Guo, Bing Zhao, Zhiyang Wang, Hongzhi Fang, Zhiyou |
author_sort | Chen, Xueran |
collection | PubMed |
description | Emerging evidence suggests that alternative splicing (AS) is modified in cancer and is associated with cancer progression. Systematic analysis of AS signature in glioblastoma (GBM) is lacking and is greatly needed. We profiled genome-wide AS events in 498 GBM patients in TCGA using RNA-seq data, and splicing network and prognostic predictor were built by integrated bioinformatics analysis. Among 45,610 AS events in 10,434 genes, we detected 1,829 AS events in 1,311 genes, and 1,667 AS events in 1,146 genes that were significantly associated with overall survival and disease-free survival of GBM patients, respectively. Five potential feature genes, S100A4, ECE2, CAST, ASPH, and LY6K, were discovered after network mining as well as correlation analysis between AS and gene expression, most of which were related to carcinogenesis and development. Multivariate survival model analysis indicated that these five feature genes could classify the prognosis at AS event and gene expression level. This report opens up a new avenue for exploration of the pathogenesis of GBM through AS, thus more precisely guiding clinical treatment and prognosis judgment. |
format | Online Article Text |
id | pubmed-6769083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67690832019-10-11 Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis Chen, Xueran Zhao, Chenggang Guo, Bing Zhao, Zhiyang Wang, Hongzhi Fang, Zhiyou Front Oncol Oncology Emerging evidence suggests that alternative splicing (AS) is modified in cancer and is associated with cancer progression. Systematic analysis of AS signature in glioblastoma (GBM) is lacking and is greatly needed. We profiled genome-wide AS events in 498 GBM patients in TCGA using RNA-seq data, and splicing network and prognostic predictor were built by integrated bioinformatics analysis. Among 45,610 AS events in 10,434 genes, we detected 1,829 AS events in 1,311 genes, and 1,667 AS events in 1,146 genes that were significantly associated with overall survival and disease-free survival of GBM patients, respectively. Five potential feature genes, S100A4, ECE2, CAST, ASPH, and LY6K, were discovered after network mining as well as correlation analysis between AS and gene expression, most of which were related to carcinogenesis and development. Multivariate survival model analysis indicated that these five feature genes could classify the prognosis at AS event and gene expression level. This report opens up a new avenue for exploration of the pathogenesis of GBM through AS, thus more precisely guiding clinical treatment and prognosis judgment. Frontiers Media S.A. 2019-09-24 /pmc/articles/PMC6769083/ /pubmed/31608231 http://dx.doi.org/10.3389/fonc.2019.00928 Text en Copyright © 2019 Chen, Zhao, Guo, Zhao, Wang and Fang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Chen, Xueran Zhao, Chenggang Guo, Bing Zhao, Zhiyang Wang, Hongzhi Fang, Zhiyou Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis |
title | Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis |
title_full | Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis |
title_fullStr | Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis |
title_full_unstemmed | Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis |
title_short | Systematic Profiling of Alternative mRNA Splicing Signature for Predicting Glioblastoma Prognosis |
title_sort | systematic profiling of alternative mrna splicing signature for predicting glioblastoma prognosis |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769083/ https://www.ncbi.nlm.nih.gov/pubmed/31608231 http://dx.doi.org/10.3389/fonc.2019.00928 |
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