microRNA-7 Inhibits the Epidermal Growth Factor Receptor and the Akt Pathway and Is Down-regulated in Glioblastoma

Benjamin Kefas(University of Virginia Health System), Jakub Godlewski(The Ohio State University Wexner Medical Center), Laurey Comeau(University of Virginia Health System), Yunqing Li(University of Virginia Health System), Roger Abounader(University of Virginia Health System), Michael P. Hawkinson(University of Virginia Health System), Jeongwu Lee(National Cancer Institute), Howard A. Fine(National Cancer Institute), E. Antonio Chiocca(The Ohio State University Wexner Medical Center), Sean Lawler(The Ohio State University Wexner Medical Center), Benjamin Purow(University of Virginia Health System)
Cancer Research
May 15, 2008
Cited by 739Open Access
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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.


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