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A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients
Long non-coding RNAs (lncRNAs) have been implicated in a variety of biological processes, and dysregulated lncRNAs have demonstrated potential roles as biomarkers and therapeutic targets for cancer prognosis and treatment. In this study, by repurposing microarray probes, we analyzed lncRNA expressio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637883/ https://www.ncbi.nlm.nih.gov/pubmed/26549855 http://dx.doi.org/10.1038/srep16553 |
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author | Sun, Jie Chen, Xihai Wang, Zhenzhen Guo, Maoni Shi, Hongbo Wang, Xiaojun Cheng, Liang Zhou, Meng |
author_facet | Sun, Jie Chen, Xihai Wang, Zhenzhen Guo, Maoni Shi, Hongbo Wang, Xiaojun Cheng, Liang Zhou, Meng |
author_sort | Sun, Jie |
collection | PubMed |
description | Long non-coding RNAs (lncRNAs) have been implicated in a variety of biological processes, and dysregulated lncRNAs have demonstrated potential roles as biomarkers and therapeutic targets for cancer prognosis and treatment. In this study, by repurposing microarray probes, we analyzed lncRNA expression profiles of 916 breast cancer patients from the Gene Expression Omnibus (GEO). Nine lncRNAs were identified to be significantly associated with metastasis-free survival (MFS) in the training dataset of 254 patients using the Cox proportional hazards regression model. These nine lncRNAs were then combined to form a single prognostic signature for predicting metastatic risk in breast cancer patients that was able to classify patients in the training dataset into high- and low-risk subgroups with significantly different MFSs (median 2.4 years versus 3.0 years, log-rank test p < 0.001). This nine-lncRNA signature was similarly effective for prognosis in a testing dataset and two independent datasets. Further analysis showed that the predictive ability of the signature was independent of clinical variables, including age, ER status, ESR1 status and ERBB2 status. Our results indicated that lncRNA signature could be a useful prognostic marker to predict metastatic risk in breast cancer patients and may improve upon our understanding of the molecular mechanisms underlying breast cancer metastasis. |
format | Online Article Text |
id | pubmed-4637883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46378832015-11-30 A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients Sun, Jie Chen, Xihai Wang, Zhenzhen Guo, Maoni Shi, Hongbo Wang, Xiaojun Cheng, Liang Zhou, Meng Sci Rep Article Long non-coding RNAs (lncRNAs) have been implicated in a variety of biological processes, and dysregulated lncRNAs have demonstrated potential roles as biomarkers and therapeutic targets for cancer prognosis and treatment. In this study, by repurposing microarray probes, we analyzed lncRNA expression profiles of 916 breast cancer patients from the Gene Expression Omnibus (GEO). Nine lncRNAs were identified to be significantly associated with metastasis-free survival (MFS) in the training dataset of 254 patients using the Cox proportional hazards regression model. These nine lncRNAs were then combined to form a single prognostic signature for predicting metastatic risk in breast cancer patients that was able to classify patients in the training dataset into high- and low-risk subgroups with significantly different MFSs (median 2.4 years versus 3.0 years, log-rank test p < 0.001). This nine-lncRNA signature was similarly effective for prognosis in a testing dataset and two independent datasets. Further analysis showed that the predictive ability of the signature was independent of clinical variables, including age, ER status, ESR1 status and ERBB2 status. Our results indicated that lncRNA signature could be a useful prognostic marker to predict metastatic risk in breast cancer patients and may improve upon our understanding of the molecular mechanisms underlying breast cancer metastasis. Nature Publishing Group 2015-11-09 /pmc/articles/PMC4637883/ /pubmed/26549855 http://dx.doi.org/10.1038/srep16553 Text en Copyright © 2015, 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 Sun, Jie Chen, Xihai Wang, Zhenzhen Guo, Maoni Shi, Hongbo Wang, Xiaojun Cheng, Liang Zhou, Meng A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients |
title | A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients |
title_full | A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients |
title_fullStr | A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients |
title_full_unstemmed | A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients |
title_short | A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patients |
title_sort | potential prognostic long non-coding rna signature to predict metastasis-free survival of breast cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637883/ https://www.ncbi.nlm.nih.gov/pubmed/26549855 http://dx.doi.org/10.1038/srep16553 |
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