miR-20a promotes proliferation and invasion by targeting APP in human ovarian cancer cells

Acta Biochim Biophys Sin (Shanghai). 2010 May 15;42(5):318-24. doi: 10.1093/abbs/gmq026.

Abstract

MicroRNAs (miRNAs) are emerging as a class of small regulated RNAs, and the alterations of miRNAs are implicated in the initiation and progression of human cancers. Our study shows that inhibition of miR-20a in OVCAR3 ovarian cancer cell line could suppress, whereas overexpression of miR-20a could enhance cell long-term proliferation and invasion. We also confirmed amyloid precursor protein (APP) as a direct target gene of miR- 20a. Furthermore, suppression of APP expression could also promote ovarian cancer cell proliferation and invasion, which is consistent with the results of miR-20a overexpression. Therefore, we concluded that the regulation of APP is an important mechanism for miR-20a to promote proliferation and invasion in ovarian cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Protein Precursor / drug effects*
  • Amyloid beta-Protein Precursor / genetics
  • Amyloid beta-Protein Precursor / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Female
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • MicroRNAs / pharmacology*
  • Neoplasm Invasiveness / physiopathology*
  • Oligonucleotide Array Sequence Analysis
  • Ovarian Neoplasms / pathology*

Substances

  • Amyloid beta-Protein Precursor
  • MIRN20a microRNA, human
  • MicroRNAs