microRNA expression in autonomous thyroid adenomas: Correlation with mRNA regulation

•Deregulated miRNA were identified in thyroid autonomous adenoma.•Correlations were performed between miRNA and mRNA regulation in the same tumors.•Deregulated miRNA are mostly involved in extracellular matrix organization.•Several miRNA are involved in the negative feedback of the cAMP pathway. The...

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Veröffentlicht in:Molecular and cellular endocrinology 2015-08, Vol.411, p.1-10
Hauptverfasser: Floor, Sébastien L., Trésallet, Christophe, Hébrant, Aline, Desbuleux, Alice, Libert, Frédérick, Hoang, Catherine, Capello, Matteo, Andry, Guy, van Staveren, Wilma C.G., Maenhaut, Carine
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Sprache:eng
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Zusammenfassung:•Deregulated miRNA were identified in thyroid autonomous adenoma.•Correlations were performed between miRNA and mRNA regulation in the same tumors.•Deregulated miRNA are mostly involved in extracellular matrix organization.•Several miRNA are involved in the negative feedback of the cAMP pathway. The objective of the study was to identify the deregulated miRNA in autonomous adenoma and to correlate the data with mRNA regulation. Seven autonomous adenoma with adjacent healthy thyroid tissues were investigated. Twelve miRNAs were downregulated and one was upregulated in the tumors. Combining bioinformatic mRNA target prediction and microarray data on mRNA regulations allowed to identify mRNA targets of our deregulated miRNAs. A large enrichment in mRNA encoding proteins involved in extracellular matrix organization and different phosphodiesterases were identified among these putative targets. The direct interaction between miR-101-3p and miR-144-3p and PDE4D mRNA was experimentally validated. The global miRNA profiles were not greatly modified, confirming the definition of these tumors as minimal deviation tumors. These results support a role for miRNA in the regulation of extracellular matrix proteins and tissue remodeling occurring during tumor development, and in the important negative feedback of the cAMP pathway, which limits the consequences of its constitutive activation in these tumors.
ISSN:0303-7207
1872-8057
DOI:10.1016/j.mce.2015.04.001