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Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival
Long noncoding RNAs (lncRNAs) play a crucial role in tumorigenesis. The aim of this study is to identify lncRNA signature that can predict breast cancer patient survival. RNA expression data from 1064 patients were downloaded from The Cancer Genome Atlas project. Cox regression, Kaplan–Meier, and re...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919625/ https://www.ncbi.nlm.nih.gov/pubmed/27338266 http://dx.doi.org/10.1038/srep27931 |
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author | Guo, Wenna Wang, Qiang Zhan, Yueping Chen, Xijia Yu, Qi Zhang, Jiawei Wang, Yi Xu, Xin-jian Zhu, Liucun |
author_facet | Guo, Wenna Wang, Qiang Zhan, Yueping Chen, Xijia Yu, Qi Zhang, Jiawei Wang, Yi Xu, Xin-jian Zhu, Liucun |
author_sort | Guo, Wenna |
collection | PubMed |
description | Long noncoding RNAs (lncRNAs) play a crucial role in tumorigenesis. The aim of this study is to identify lncRNA signature that can predict breast cancer patient survival. RNA expression data from 1064 patients were downloaded from The Cancer Genome Atlas project. Cox regression, Kaplan–Meier, and receiver operating characteristic (ROC) analyses were performed to construct a model for predicting the overall survival (OS) of patients and evaluate it. A model consisting of three lncRNA genes (CAT104, LINC01234, and STXBP5-AS1) was identified. The Kaplan–Meier analysis and ROC curves proved that the model could predict the prognostic survival with good sensitivity and specificity in both the validation set (AUC = 0.752, 95% confidence intervals (CI): 0.651–0.854) and the microarray dataset (AUC = 0.714, 95%CI: 0.615–0.814). Further study showed the three-lncRNA signature was not only pervasive in different breast cancer stages, subtypes and age groups, but also provides more accurate prognostic information than some widely known biomarkers. The results suggested that RNA-seq transcriptome profiling provides that the three-lncRNA signature is an independent prognostic biomarker, and have clinical significance. In addition, lncRNA, miRNA, and mRNA interaction network indicated lncRNAs may intervene in breast cancer pathogenesis by binding to miR-190b, acting as competing endogenous RNAs. |
format | Online Article Text |
id | pubmed-4919625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49196252016-06-28 Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival Guo, Wenna Wang, Qiang Zhan, Yueping Chen, Xijia Yu, Qi Zhang, Jiawei Wang, Yi Xu, Xin-jian Zhu, Liucun Sci Rep Article Long noncoding RNAs (lncRNAs) play a crucial role in tumorigenesis. The aim of this study is to identify lncRNA signature that can predict breast cancer patient survival. RNA expression data from 1064 patients were downloaded from The Cancer Genome Atlas project. Cox regression, Kaplan–Meier, and receiver operating characteristic (ROC) analyses were performed to construct a model for predicting the overall survival (OS) of patients and evaluate it. A model consisting of three lncRNA genes (CAT104, LINC01234, and STXBP5-AS1) was identified. The Kaplan–Meier analysis and ROC curves proved that the model could predict the prognostic survival with good sensitivity and specificity in both the validation set (AUC = 0.752, 95% confidence intervals (CI): 0.651–0.854) and the microarray dataset (AUC = 0.714, 95%CI: 0.615–0.814). Further study showed the three-lncRNA signature was not only pervasive in different breast cancer stages, subtypes and age groups, but also provides more accurate prognostic information than some widely known biomarkers. The results suggested that RNA-seq transcriptome profiling provides that the three-lncRNA signature is an independent prognostic biomarker, and have clinical significance. In addition, lncRNA, miRNA, and mRNA interaction network indicated lncRNAs may intervene in breast cancer pathogenesis by binding to miR-190b, acting as competing endogenous RNAs. Nature Publishing Group 2016-06-24 /pmc/articles/PMC4919625/ /pubmed/27338266 http://dx.doi.org/10.1038/srep27931 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Guo, Wenna Wang, Qiang Zhan, Yueping Chen, Xijia Yu, Qi Zhang, Jiawei Wang, Yi Xu, Xin-jian Zhu, Liucun Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival |
title | Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival |
title_full | Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival |
title_fullStr | Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival |
title_full_unstemmed | Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival |
title_short | Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival |
title_sort | transcriptome sequencing uncovers a three–long noncoding rna signature in predicting breast cancer survival |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919625/ https://www.ncbi.nlm.nih.gov/pubmed/27338266 http://dx.doi.org/10.1038/srep27931 |
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