MiR-483-5p suppresses the proliferation of glioma cells via directly targeting ERK1

FEBS Lett. 2012 May 7;586(9):1312-7. doi: 10.1016/j.febslet.2012.03.035. Epub 2012 Mar 27.

Abstract

MicroRNAs (miRNAs) exhibit tumor-specific expression signatures and play crucial roles in tumorigenesis by targeting oncogenes. Here, through analyzing the miRNA-array profiles of human glioblastoma tissues and the adjacent normal brain tissues, we found miR-483-5p was significantly down-regulated in gliomas, which was confirmed in both human glioma specimens and cell lines. The overexpression of miR-483-5p suppressed glioma cell proliferation and induced a G0/G1 arrest. In contrast, miR-483-5p inhibition promoted cell proliferation. Furthermore, by a dual-luciferase reporter assay and expression analysis, we identified extracellular signal-regulated kinase 1 (ERK1) as a direct target of miR-483-5p. ERK1 knockdown can block cell proliferation induced by miR-483-5p inhibition. Thus, our findings provide the first evidence that miR-483-5p can serve as a tumor suppressor in gliomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Brain / cytology
  • Brain / metabolism
  • Brain / pathology
  • Cell Line, Tumor
  • Cell Proliferation
  • Down-Regulation / genetics
  • G1 Phase Cell Cycle Checkpoints / genetics
  • Glioma / genetics
  • Glioma / pathology*
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism*
  • Mitogen-Activated Protein Kinase 3 / genetics*

Substances

  • MIRN483 microRNA, human
  • MicroRNAs
  • Mitogen-Activated Protein Kinase 3