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A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling
Estrogen receptor signalling plays important regulatory roles in multiple mammalian physiological processes. Dysregulation of estrogen receptor (ER) expression and/or its associated signalling pathway is strongly associated with the development, progression, transition, and endocrine-resistance of b...
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/PMC4991000/ https://www.ncbi.nlm.nih.gov/pubmed/27539025 http://dx.doi.org/10.1038/srep31716 |
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author | Wu, Liangcai Xu, Qianqian Zhang, Haohai Li, Ming Zhu, Chengpei Jiang, Minjie Sang, Xinting Zhao, Yi Sun, Qiang Zhao, Haitao |
author_facet | Wu, Liangcai Xu, Qianqian Zhang, Haohai Li, Ming Zhu, Chengpei Jiang, Minjie Sang, Xinting Zhao, Yi Sun, Qiang Zhao, Haitao |
author_sort | Wu, Liangcai |
collection | PubMed |
description | Estrogen receptor signalling plays important regulatory roles in multiple mammalian physiological processes. Dysregulation of estrogen receptor (ER) expression and/or its associated signalling pathway is strongly associated with the development, progression, transition, and endocrine-resistance of breast cancer. Non-coding transcripts are essential regulators of almost every level of gene regulation. However, few long non-coding transcripts (lncRNAs) associated with the estrogen receptor signalling pathway have been well-described. We used array-based methods to identify 33 estrogen receptor agitation-related (ERAR) lncRNAs. A coding–non-coding gene co-expression network analysis suggested that 15 ERAR lncRNAs were associated with mitosis, DNA damage, and DNA repair. Kaplan–Meier analysis indicated that five ERAR lncRNAs selected using the Random Forest-Recursive Feature Elimination algorithm were significantly correlated with endocrine resistance-free survival and distant metastasis-free survival as well as disease free survival. Our results suggest that ERAR lncRNAs may serve as novel biomarkers for guiding breast cancer treatment and prognosis. Furthermore, our findings reveal a new avenue by which estrogen receptor signalling can be further explored. |
format | Online Article Text |
id | pubmed-4991000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49910002016-08-30 A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling Wu, Liangcai Xu, Qianqian Zhang, Haohai Li, Ming Zhu, Chengpei Jiang, Minjie Sang, Xinting Zhao, Yi Sun, Qiang Zhao, Haitao Sci Rep Article Estrogen receptor signalling plays important regulatory roles in multiple mammalian physiological processes. Dysregulation of estrogen receptor (ER) expression and/or its associated signalling pathway is strongly associated with the development, progression, transition, and endocrine-resistance of breast cancer. Non-coding transcripts are essential regulators of almost every level of gene regulation. However, few long non-coding transcripts (lncRNAs) associated with the estrogen receptor signalling pathway have been well-described. We used array-based methods to identify 33 estrogen receptor agitation-related (ERAR) lncRNAs. A coding–non-coding gene co-expression network analysis suggested that 15 ERAR lncRNAs were associated with mitosis, DNA damage, and DNA repair. Kaplan–Meier analysis indicated that five ERAR lncRNAs selected using the Random Forest-Recursive Feature Elimination algorithm were significantly correlated with endocrine resistance-free survival and distant metastasis-free survival as well as disease free survival. Our results suggest that ERAR lncRNAs may serve as novel biomarkers for guiding breast cancer treatment and prognosis. Furthermore, our findings reveal a new avenue by which estrogen receptor signalling can be further explored. Nature Publishing Group 2016-08-19 /pmc/articles/PMC4991000/ /pubmed/27539025 http://dx.doi.org/10.1038/srep31716 Text en Copyright © 2016, The Author(s) 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 Wu, Liangcai Xu, Qianqian Zhang, Haohai Li, Ming Zhu, Chengpei Jiang, Minjie Sang, Xinting Zhao, Yi Sun, Qiang Zhao, Haitao A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling |
title | A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling |
title_full | A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling |
title_fullStr | A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling |
title_full_unstemmed | A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling |
title_short | A new avenue for obtaining insight into the functional characteristics of long noncoding RNAs associated with estrogen receptor signaling |
title_sort | new avenue for obtaining insight into the functional characteristics of long noncoding rnas associated with estrogen receptor signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991000/ https://www.ncbi.nlm.nih.gov/pubmed/27539025 http://dx.doi.org/10.1038/srep31716 |
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