Abstract

Abstract microRNAs are noncoding RNAs inhibiting expression of numerous target genes, and a few have been shown to act as oncogenes or tumor suppressors. We show that microRNA-7 (miR-7) is a potential tumor suppressor in glioblastoma targeting critical cancer pathways. miR-7 potently suppressed epidermal growth factor receptor expression, and furthermore it independently inhibited the Akt pathway via targeting upstream regulators. miR-7 expression was down-regulated in glioblastoma versus surrounding brain, with a mechanism involving impaired processing. Importantly, transfection with miR-7 decreased viability and invasiveness of primary glioblastoma lines. This study establishes miR-7 as a regulator of major cancer pathways and suggests that it has therapeutic potential for glioblastoma. [Cancer Res 2008;68(10):3566–71]

Keywords

microRNACancer researchEpidermal growth factor receptorProtein kinase BBiologyGliomaTransfectionSuppressorCancerSignal transductionRegulatorDownregulation and upregulationGlioblastomaGeneCell biologyGenetics

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Publication Info

Year
2008
Type
article
Volume
68
Issue
10
Pages
3566-3572
Citations
734
Access
Closed

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Benjamin Kefas, Jakub Godlewski, Laurey Comeau et al. (2008). microRNA-7 Inhibits the Epidermal Growth Factor Receptor and the Akt Pathway and Is Down-regulated in Glioblastoma. Cancer Research , 68 (10) , 3566-3572. https://doi.org/10.1158/0008-5472.can-07-6639

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DOI
10.1158/0008-5472.can-07-6639