Cargando…
A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator
MiRNAs are key regulators of gene expression. By binding to many genes, they create a complex network of gene co-regulation. Here, using a network-based approach, we identified miRNA hub groups by their close connections and common targets. In one cluster containing three miRNAs, miR-612, miR-661 an...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389139/ https://www.ncbi.nlm.nih.gov/pubmed/25673565 http://dx.doi.org/10.1038/srep08336 |
_version_ | 1782521236890320896 |
---|---|
author | Bhajun, Ricky Guyon, Laurent Pitaval, Amandine Sulpice, Eric Combe, Stéphanie Obeid, Patricia Haguet, Vincent Ghorbel, Itebeddine Lajaunie, Christian Gidrol, Xavier |
author_facet | Bhajun, Ricky Guyon, Laurent Pitaval, Amandine Sulpice, Eric Combe, Stéphanie Obeid, Patricia Haguet, Vincent Ghorbel, Itebeddine Lajaunie, Christian Gidrol, Xavier |
author_sort | Bhajun, Ricky |
collection | PubMed |
description | MiRNAs are key regulators of gene expression. By binding to many genes, they create a complex network of gene co-regulation. Here, using a network-based approach, we identified miRNA hub groups by their close connections and common targets. In one cluster containing three miRNAs, miR-612, miR-661 and miR-940, the annotated functions of the co-regulated genes suggested a role in small GTPase signalling. Although the three members of this cluster targeted the same subset of predicted genes, we showed that their overexpression impacted cell fates differently. miR-661 demonstrated enhanced phosphorylation of myosin II and an increase in cell invasion, indicating a possible oncogenic miRNA. On the contrary, miR-612 and miR-940 inhibit phosphorylation of myosin II and cell invasion. Finally, expression profiling in human breast tissues showed that miR-940 was consistently downregulated in breast cancer tissues |
format | Online Article Text |
id | pubmed-5389139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53891392017-04-14 A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator Bhajun, Ricky Guyon, Laurent Pitaval, Amandine Sulpice, Eric Combe, Stéphanie Obeid, Patricia Haguet, Vincent Ghorbel, Itebeddine Lajaunie, Christian Gidrol, Xavier Sci Rep Article MiRNAs are key regulators of gene expression. By binding to many genes, they create a complex network of gene co-regulation. Here, using a network-based approach, we identified miRNA hub groups by their close connections and common targets. In one cluster containing three miRNAs, miR-612, miR-661 and miR-940, the annotated functions of the co-regulated genes suggested a role in small GTPase signalling. Although the three members of this cluster targeted the same subset of predicted genes, we showed that their overexpression impacted cell fates differently. miR-661 demonstrated enhanced phosphorylation of myosin II and an increase in cell invasion, indicating a possible oncogenic miRNA. On the contrary, miR-612 and miR-940 inhibit phosphorylation of myosin II and cell invasion. Finally, expression profiling in human breast tissues showed that miR-940 was consistently downregulated in breast cancer tissues Nature Publishing Group 2015-02-12 /pmc/articles/PMC5389139/ /pubmed/25673565 http://dx.doi.org/10.1038/srep08336 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bhajun, Ricky Guyon, Laurent Pitaval, Amandine Sulpice, Eric Combe, Stéphanie Obeid, Patricia Haguet, Vincent Ghorbel, Itebeddine Lajaunie, Christian Gidrol, Xavier A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator |
title | A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator |
title_full | A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator |
title_fullStr | A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator |
title_full_unstemmed | A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator |
title_short | A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator |
title_sort | statistically inferred microrna network identifies breast cancer target mir-940 as an actin cytoskeleton regulator |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389139/ https://www.ncbi.nlm.nih.gov/pubmed/25673565 http://dx.doi.org/10.1038/srep08336 |
work_keys_str_mv | AT bhajunricky astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT guyonlaurent astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT pitavalamandine astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT sulpiceeric astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT combestephanie astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT obeidpatricia astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT haguetvincent astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT ghorbelitebeddine astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT lajauniechristian astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT gidrolxavier astatisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT bhajunricky statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT guyonlaurent statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT pitavalamandine statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT sulpiceeric statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT combestephanie statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT obeidpatricia statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT haguetvincent statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT ghorbelitebeddine statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT lajauniechristian statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator AT gidrolxavier statisticallyinferredmicrornanetworkidentifiesbreastcancertargetmir940asanactincytoskeletonregulator |