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Issue 1, 2015
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Identification of miR-145 targets through an integrated omics analysis

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Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression and protein synthesis. To characterize functions of miRNAs and to assess their potential applications, we carried out an integrated multi-omics analysis to study miR-145, a miRNA that has been shown to suppress tumor growth. We employed gene expression profiling, miRNA profiling and quantitative proteomic analysis of a pancreatic cancer cell line. In our transcriptomic analysis, overexpression of miR-145 was found to suppress the expression of genes that are implicated in development of cancer such as ITGA11 and MAGEA4 in addition to previously described targets such as FSCN1, YES1 and PODXL. Based on miRNA profiling, overexpression of miR-145 also upregulated other miRNAs including miR-124, miR-133b and miR-125a-3p, all of which are implicated in suppression of tumors and are generally co-regulated with miR-145 in other cancers. Using the SILAC system, we identified miR-145-induced downregulation of several oncoproteins/cancer biomarkers including SET, RPA1, MCM2, ABCC1, SPTBN1 and SPTLC1. Luciferase assay validation carried out on a subset of downregulated candidate targets confirmed them to be novel direct targets of miR-145. Overall, this multi-omics approach provided insights into miR-145-mediated tumor suppression and could be used as a general strategy to study the targets of individual miRNAs.

Graphical abstract: Identification of miR-145 targets through an integrated omics analysis

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Publication details

The article was received on 02 Oct 2014, accepted on 18 Oct 2014 and first published on 23 Oct 2014


Article type: Paper
DOI: 10.1039/C4MB00585F
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Citation: Mol. BioSyst., 2015,11, 197-207
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    Identification of miR-145 targets through an integrated omics analysis

    T. Huang, S. Renuse, S. Pinto, P. Kumar, Y. Yang, R. Chaerkady, B. Godsey, J. T. Mendell, M. K. Halushka, C. I. Civin, L. Marchionni and A. Pandey, Mol. BioSyst., 2015, 11, 197
    DOI: 10.1039/C4MB00585F

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