MicroRNA-21 expression is regulated by β-catenin/STAT3 pathway and promotes glioma cell invasion by direct targeting RECK

CNS Neurosci Ther. 2012 Jul;18(7):573-83. doi: 10.1111/j.1755-5949.2012.00344.x. Epub 2012 May 28.

Abstract

Aims: MicroRNA-21 (miR-21) expression is increased in many types of human malignancy, including glioma. Recent studies report that miR-21 regulates cell invasion by targeting RECK, however, the underlying transcriptional regulation of miR-21 in glioma cells remains elusive.

Results: Here, we identify a positive correlation between miR-21 expression and pathological grade in glioma tissues. We demonstrate that β-catenin pathway regulates miR-21 expression in human umbilical vein endothelial cell and glioma cells, and that this regulation is signal transducer and activator of transcription 3 (STAT3)-dependent. Further, chromatin immunoprecipitation and luciferase reporter analysis demonstrate that miR-21 is controlled by an upstream promoter containing a conserved STAT3 binding site. Notably, knockdown of miR-21-inhibited cell invasion by increasing RECK expression and decreased tumor growth in a xenograft model.

Conclusion: These data provide compelling evidence that β-catenin regulation of miR-21 via STAT3 plays a role in glioma cell invasion and proliferation and indicate that STAT3 is a potential therapeutic target for glioma intervention.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Down-Regulation / genetics
  • GPI-Linked Proteins / genetics
  • GPI-Linked Proteins / metabolism*
  • Gene Expression Regulation, Neoplastic*
  • Gene Knockdown Techniques / methods
  • Gene Targeting / methods
  • Glioma / genetics
  • Glioma / metabolism*
  • Glioma / pathology
  • Humans
  • Mice
  • Mice, Nude
  • MicroRNAs / biosynthesis
  • MicroRNAs / metabolism*
  • Neoplasm Invasiveness / genetics
  • Neoplasm Invasiveness / pathology
  • STAT3 Transcription Factor / physiology*
  • Umbilical Veins / cytology
  • Umbilical Veins / metabolism
  • Up-Regulation / genetics
  • Xenograft Model Antitumor Assays / methods
  • beta Catenin / physiology*

Substances

  • CTNNB1 protein, human
  • GPI-Linked Proteins
  • MIRN21 microRNA, human
  • MicroRNAs
  • RECK protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • beta Catenin