The tumor suppressor role of miR-124 in osteosarcoma

PLoS One. 2014 Jun 27;9(6):e91566. doi: 10.1371/journal.pone.0091566. eCollection 2014.

Abstract

MicroRNAs have crucial roles in development and progression of human cancers, including osteosarcoma. Recent studies have shown that miR-124 was down-regulated in many cancers; however, the role of miR-124 in osteosarcoma development is unknown. In this study, we demonstrate that expression of miR-124 is significantly downregulated in osteosarcoma tissues and cell lines, compared to the adjacent tissues. The expression of miR-124 in the metastases osteosarcoma tissues was lower than that in non- metastases tissues. We identified and confirmed Rac1 as a novel, direct target of miR-124 using prediction algorithms and luciferase reporter gene assays. Overexpression of miR-124 suppressed Rac1 protein expression and attenuated cell proliferation, migration, and invasion and induced apoptosis in MG-63 and U2OS in vitro. Moreover, overexpression of Rac1 in miR-124-transfected osteosarcoma cells effectively rescued the inhibition of cell invasion caused by miR-124. Therefore, our results demonstrate that miR-124 is a tumor suppressor miRNA and suggest that this miRNA could be a potential target for the treatment of osteosarcoma in future.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Adolescent
  • Apoptosis
  • Cell Line, Tumor
  • Child
  • Female
  • Genes, Tumor Suppressor*
  • Humans
  • Male
  • MicroRNAs / genetics*
  • Neoplasm Metastasis
  • Osteosarcoma / genetics*
  • Osteosarcoma / metabolism
  • Osteosarcoma / pathology
  • rac1 GTP-Binding Protein / genetics
  • rac1 GTP-Binding Protein / metabolism

Substances

  • MIRN124 microRNA, human
  • MicroRNAs
  • RAC1 protein, human
  • rac1 GTP-Binding Protein

Grants and funding

This study is supported by National Natural Science Foundation of China (81271984) and Research Fund for the Doctoral Program of Higher Education of China (20122307120036) and Natural Science Foundation for Returness of Heilongjiang Province of China (LC2012C11), Research Fund of the First Affiliated Hospital of Harbin Medical University (2013LX01), Heilongjiang Postdoctoral Financial Assistance (Grant Number: LBH-Z13143), and China Postdoctoral Science Foundation (Grant Number: 2014M551275). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.