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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...

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Autores principales: Bhajun, Ricky, Guyon, Laurent, Pitaval, Amandine, Sulpice, Eric, Combe, Stéphanie, Obeid, Patricia, Haguet, Vincent, Ghorbel, Itebeddine, Lajaunie, Christian, Gidrol, Xavier
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
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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
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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
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