Identification of let-7-regulated oncofetal genes

MicroRNAs (miRNA) are small RNA molecules of approximately 20 to 22 nucleotides that reduce expression of proteins through mRNA degradation and/or translational silencing. Each known miRNA has a large number of predicted targets. Members of the let-7/miR-98 family of miRNAs are up-regulated at the e...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2008-04, Vol.68 (8), p.2587-2591
Hauptverfasser: Boyerinas, Benjamin, Park, Sun-Mi, Shomron, Noam, Hedegaard, Mads M, Vinther, Jeppe, Andersen, Jens S, Feig, Christine, Xu, Jinbo, Burge, Christopher B, Peter, Marcus E
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Sprache:eng
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Zusammenfassung:MicroRNAs (miRNA) are small RNA molecules of approximately 20 to 22 nucleotides that reduce expression of proteins through mRNA degradation and/or translational silencing. Each known miRNA has a large number of predicted targets. Members of the let-7/miR-98 family of miRNAs are up-regulated at the end of embryonic development. Let-7 is often down-regulated early during cancer development, suggesting that let-7-regulated oncofetal genes (LOG) may become reexpressed in cancer cells. Using comparative bioinformatics, we have identified 12 conserved LOGs that include HMGA2 and IMP-1/CRD-BP. IMP-1 has growth-promoting activities through stabilization of c-myc mRNA. We experimentally confirmed that IMP-1 is a direct let-7 target that promotes cell growth and motility of tumor cells, and we confirmed by proteomics analysis that IMP-1 and HMGA2 are major miRNA targets. Our data suggest that a substantial part of the growth inhibitory activities of let-7 comes from suppressing the expression of IMP-1. LOGs could be novel therapeutic targets and potential biomarkers for cancer treatment.
ISSN:0008-5472
1538-7445
DOI:10.1158/0008-5472.CAN-08-0264