Genome-wide analysis reveals downregulation of miR-379/miR-656 cluster in human cancers

MicroRNAs (miRNAs) are non-uniformly distributed in genomes and ~30% of the miRNAs in the human genome are clustered. In this study we have focused on the imprinted miRNA cluster miR-379/miR-656 on 14q32.31 (hereafter C14) to test their coordinated function. We have analyzed expression profile of &g...

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Veröffentlicht in:Biology direct 2013-04, Vol.8 (1), p.10-10, Article 10
Hauptverfasser: Laddha, Saurabh V, Nayak, Subhashree, Paul, Deepanjan, Reddy, Rajasekhara, Sharma, Charu, Jha, Prerana, Hariharan, Manoj, Agrawal, Anurag, Chowdhury, Shantanu, Sarkar, Chitra, Mukhopadhyay, Arijit
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Sprache:eng
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Zusammenfassung:MicroRNAs (miRNAs) are non-uniformly distributed in genomes and ~30% of the miRNAs in the human genome are clustered. In this study we have focused on the imprinted miRNA cluster miR-379/miR-656 on 14q32.31 (hereafter C14) to test their coordinated function. We have analyzed expression profile of >1000 human miRNAs in >1400 samples representing seven different human tissue types obtained from cancer patients along with matched and unmatched controls. We found 68% of the miRNAs in this cluster to be significantly downregulated in glioblastoma multiforme (GBM), 61% downregulated in kidney renal clear cell carcinoma (KIRC), 46% in breast invasive carcinoma (BRCA) and 14% in ovarian serous cystadenocarcinoma (OV). On a genome-wide scale C14 miRNAs accounted for 12-30% of the total downregulated miRNAs in different cancers. Pathway enrichment for the predicted targets of C14 miRNA was significant for cancer pathways, especially Glioma (p< 3.77x10⁻⁶, FDR
ISSN:1745-6150
1745-6150
DOI:10.1186/1745-6150-8-10