miR-17 inhibitor suppressed osteosarcoma tumor growth and metastasis via increasing PTEN expression

Biochem Biophys Res Commun. 2014 Feb 7;444(2):230-4. doi: 10.1016/j.bbrc.2014.01.061. Epub 2014 Jan 22.

Abstract

MicroRNAs (miRNAs) play essential roles in cancer development and progression. Here, we investigated the role of miR-17 in the progression and metastasis of osteosarcoma (OS). miR-17 was frequently increased in OS tissues and cell lines. Inhibition of miR-17 in OS cell lines substantially suppressed cell proliferation, migration, and invasion. Phosphatase and tensin homolog (PTEN) was identified as a target of miR-17, and ectopic expression of miR-17 inhibited PTEN by direct binding to its 3'-untranslated region (3'-UTR). Expression of miR-17 was negatively correlated with PTEN in OS tissues. Together, these findings indicate that miR-17 acts as an oncogenic miRNA and may contribute to the progression and metastasis of OS, suggesting miR-17 as a potential novel diagnostic and therapeutic target of OS.

Keywords: Invasion; Migration; Osteosarcoma; PTEN; Proliferation; miR-17.

MeSH terms

  • 3' Untranslated Regions / genetics
  • Base Sequence
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation*
  • Gene Expression Regulation, Neoplastic*
  • HEK293 Cells
  • Humans
  • Immunoblotting
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Neoplasm Metastasis
  • Osteosarcoma / genetics*
  • Osteosarcoma / metabolism
  • Osteosarcoma / pathology
  • PTEN Phosphohydrolase / genetics*
  • PTEN Phosphohydrolase / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Nucleic Acid
  • Tumor Burden / genetics

Substances

  • 3' Untranslated Regions
  • MIRN17 microRNA, human
  • MicroRNAs
  • PTEN Phosphohydrolase