Sustained expression of miR-26a promotes chromosomal instability and tumorigenesis through regulation of CHFR

Nucleic Acids Res. 2017 May 5;45(8):4401-4412. doi: 10.1093/nar/gkx022.

Abstract

MicroRNA 26a (miR-26a) reduces cell viability in several cancers, indicating that miR-26a could be used as a therapeutic option in patients. We demonstrate that miR-26a not only inhibits G1-S cell cycle transition and promotes apoptosis, as previously described, but also regulates multiple cell cycle checkpoints. We show that sustained miR-26a over-expression in both breast cancer (BC) cell lines and mouse embryonic fibroblasts (MEFs) induces oversized cells containing either a single-large nucleus or two nuclei, indicating defects in mitosis and cytokinesis. Additionally, we demonstrate that miR-26a induces aneuploidy and centrosome defects and enhances tumorigenesis. Mechanistically, it acts by targeting G1-S transition genes as well as genes involved in mitosis and cytokinesis such as CHFR, LARP1 and YWHAE. Importantly, we show that only the re-expression of CHFR in miR-26a over-expressing cells partially rescues normal mitosis and impairs the tumorigenesis exerted by miR-26a, indicating that CHFR represents an important miR-26a target in the regulation of such phenotypes. We propose that miR-26a delivery might not be a viable therapeutic strategy due to the potential deleterious oncogenic activity of this miRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins / genetics
  • 14-3-3 Proteins / metabolism
  • Animals
  • Autoantigens / genetics
  • Autoantigens / metabolism
  • Carcinogenesis / genetics*
  • Carcinogenesis / metabolism
  • Carcinogenesis / pathology
  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Cell Size
  • Chromosomal Instability*
  • Female
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • G1 Phase Cell Cycle Checkpoints
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • MCF-7 Cells
  • Mice
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Mitosis
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Poly-ADP-Ribose Binding Proteins
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / metabolism
  • SS-B Antigen
  • Sequence Analysis, RNA
  • Signal Transduction
  • Ubiquitin-Protein Ligases

Substances

  • 14-3-3 Proteins
  • Autoantigens
  • Cell Cycle Proteins
  • MIRN26A microRNA, human
  • MicroRNAs
  • Neoplasm Proteins
  • Poly-ADP-Ribose Binding Proteins
  • Ribonucleoproteins
  • YWHAE protein, human
  • CHFR protein, human
  • Ubiquitin-Protein Ligases