The Downregulation of MiR-182 Is Associated with the Growth and Invasion of Osteosarcoma Cells through the Regulation of TIAM1 Expression

PLoS One. 2015 May 14;10(5):e0121175. doi: 10.1371/journal.pone.0121175. eCollection 2015.

Abstract

Background: Osteosarcoma is the most common primary bone malignancy in children and young adults. Increasing results suggest that discovery of microRNAs (miRNAs) might provide a novel therapeutical target for osteosarcoma.

Methods: MiR-182 expression level in osteosarcoma cell lines and tissues were assayed by qRT-PCR. MiRNA mimics or inhibitor were transfected for up-regulation or down-regulation of miR-182 expression. Cell function was assayed by CCK8, migration assay and invasion assay. The target genes of miR-182 were predicated by bioinformatics algorithm (TargetScan Human).

Results: MiR-182 was down-regulated in osteosarcoma tissues and cell lines. Overexpression of miR-182 inhibited tumor growth, migration and invasion. Subsequent investigation revealed that TIAM1 was a direct and functional target of miR-182 in osteosarcoma cells. Overexpression of miR-182 impaired TIAM1-induced inhibition of proliferation and invasion in osteosarcoma cells.

Conclusions: Down-expression of miR-182 in osteosarcoma promoted tumor growth, migration and invasion by targeting TIAM1. MiR-182 might act as a tumor suppressor gene whose down-regulation contributes to the progression and metastasis of osteosarcoma, providing a potential therapy target for osteosarcoma patients.

Publication types

  • Retracted Publication

MeSH terms

  • Adolescent
  • Bone Neoplasms / genetics*
  • Bone Neoplasms / metabolism
  • Bone Neoplasms / pathology
  • Cell Movement
  • Cell Proliferation
  • Child
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Guanine Nucleotide Exchange Factors / genetics*
  • Guanine Nucleotide Exchange Factors / metabolism
  • Humans
  • Male
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Molecular Mimicry
  • Neoplasm Invasiveness
  • Oligoribonucleotides / genetics
  • Oligoribonucleotides / metabolism
  • Osteosarcoma / genetics*
  • Osteosarcoma / metabolism
  • Primary Cell Culture
  • Signal Transduction
  • T-Lymphoma Invasion and Metastasis-inducing Protein 1
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Guanine Nucleotide Exchange Factors
  • MicroRNAs
  • Mirn182 microRNA, human
  • Oligoribonucleotides
  • T-Lymphoma Invasion and Metastasis-inducing Protein 1
  • TIAM1 protein, human

Grants and funding

The authors received no specific funding for this work.