MiR-194-5p inhibits cell migration and invasion in bladder cancer by targeting E2F3

J BUON. 2018 Sep-Oct;23(5):1492-1499.

Abstract

Purpose: MicroRNA (miR)-194-5p is downregulated in bladder cancer (BC), but its role in BC has not been determined mechanistically.

Methods: The expression levels of miR-194-5p and E2F transcription factor 3 (E2F3) were determined by means of quantitative reverse transcription and polymerase chain reaction in BC specimens. In addition, T24 BC cells were transfected with a miR-194-5p mimic, a miR-194-5p inhibitor, or E2F3 small interfering (si)RNA, and the level of E2F3 protein expressed by these cells was assessed by western blotting. A dual luciferase reporter assay was applied to verify the binding site between miR-194-5p and the 3' untranslated region of E2F3. Transwell assays were performed to examine cell migration and invasion.

Results: Dysregulation of miR-194-5p in BC was closely associated with node metastasis and differentiation. In BC specimens and cell lines, miR-194-5p mRNA was downregulated, while E2F3 mRNA was upregulated. Overexpression of miR-194-5p suppressed the expression of E2F3 mRNA and protein. By regulating E2F3, miR-194-5p inhibited cell migration and invasion in BC. Treatment of BC cells with E2F3 siRNA had the same effect as did overexpression of miR-194-5p.

Conclusions: MiR-194-5p directly targets E2F3 and inhibits cell migration and invasion in BC.

MeSH terms

  • Cell Movement / physiology
  • Down-Regulation
  • E2F3 Transcription Factor / antagonists & inhibitors
  • E2F3 Transcription Factor / biosynthesis
  • E2F3 Transcription Factor / genetics
  • E2F3 Transcription Factor / metabolism*
  • Humans
  • MicroRNAs / biosynthesis
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Neoplasm Invasiveness
  • Transfection
  • Urinary Bladder Neoplasms / genetics*
  • Urinary Bladder Neoplasms / metabolism*
  • Urinary Bladder Neoplasms / pathology

Substances

  • E2F3 Transcription Factor
  • E2F3 protein, human
  • MIRN194 microRNA, human
  • MicroRNAs