MiR-522 contributes to cell proliferation of human glioblastoma cells by suppressing PHLPP1 expression

Biomed Pharmacother. 2015 Mar:70:164-9. doi: 10.1016/j.biopha.2015.01.017. Epub 2015 Jan 13.

Abstract

Previous studies have shown that microRNAs play essential roles in cancer growth and progression. Although a number of microRNAs were differentially expressed in glioblastoma (GBM). In this study, we evaluated the miR-522s role in cell proliferation in GBM. Expression of miR-522 is markedly upregulated in GBM tissues and GBM cells compared with the matched non-tumor adjacent brain tissues (TAT) and normal human astrocytes (NHAs). In functional assays, miR-522 promoted GBM cell proliferation, which could be reversed by inhibitor of miR-522. We further identified PH domain leucine-rich repeats protein phosphatase-1 (PHLPP1) as a putative target of miR-522, which is likely a main contributor to the promotion of tumor cell growth observed in our assays. Our results demonstrated that miR-522 promoted tumor cell proliferation and hence may represent a novel therapeutically relevant cellular target to treatment of GBM patients.

Keywords: Cell proliferation; Glioblastoma; PHLPP1; miR-522.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Proliferation / physiology*
  • Gene Expression Regulation, Neoplastic*
  • Glioblastoma / metabolism*
  • Glioblastoma / pathology
  • Humans
  • MicroRNAs / physiology*
  • Nuclear Proteins / biosynthesis*
  • Phosphoprotein Phosphatases / biosynthesis*

Substances

  • MIRN522 microRNA, human
  • MicroRNAs
  • Nuclear Proteins
  • PHLPP1 protein, human
  • Phosphoprotein Phosphatases