An NF90/NF110-mediated feedback amplification loop regulates dicer expression and controls ovarian carcinoma progression

Cell Res. 2018 May;28(5):556-571. doi: 10.1038/s41422-018-0016-8. Epub 2018 Mar 21.

Abstract

Reduced expression of DICER, a key enzyme in the miRNA pathway, is frequently associated with aggressive, invasive disease, and poor survival in various malignancies. Regulation of DICER expression is, however, poorly understood. Here, we show that NF90/NF110 facilitates DICER expression by controlling the processing of a miRNA, miR-3173, which is embedded in DICER pre-mRNA. As miR-3173 in turn targets NF90, a feedback amplification loop controlling DICER expression is established. In a nude mouse model, NF90 overexpression reduced proliferation of ovarian cancer cells and significantly reduced tumor size and metastasis, whereas overexpression of miR-3173 dramatically increased metastasis in an NF90- and DICER-dependent manner. Clinically, low NF90 expression and high miR-3173-3p expression were found to be independent prognostic markers of poor survival in a cohort of ovarian carcinoma patients. These findings suggest that, by facilitating DICER expression, NF90 can act as a suppressor of ovarian carcinoma.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line, Tumor
  • Cell Movement
  • Disease Progression*
  • Feedback, Physiological*
  • Female
  • HEK293 Cells
  • Humans
  • Mice, Inbred BALB C
  • Mice, Nude
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Models, Biological
  • Neoplasm Metastasis
  • Nuclear Factor 90 Proteins / metabolism*
  • Ovarian Neoplasms / genetics
  • Ovarian Neoplasms / pathology*
  • RNA Precursors / genetics
  • RNA Precursors / metabolism
  • RNA Splicing / genetics
  • Ribonuclease III / genetics
  • Ribonuclease III / metabolism*
  • Treatment Outcome

Substances

  • MIRN3173 microRNA, human
  • MicroRNAs
  • Nuclear Factor 90 Proteins
  • RNA Precursors
  • Ribonuclease III