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A statistically inferred microRNA network identifies breast cancer target miR-940 as an actin cytoskeleton regulator

1 juil. 2015Scientific Reports

DOI : 10.1038/srep08336

Auteurs

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

Résumé

Abstract

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