FOXO6 promotes gastric cancer cell tumorigenicity via upregulation of C-myc

FEBS Lett. 2013 Jul 11;587(14):2105-11. doi: 10.1016/j.febslet.2013.05.027. Epub 2013 May 25.

Abstract

The aberrant regulation of many related genes is involved in the development and progression of gastric carcinoma. In the present study, we show that mRNA and protein levels of FOXO6 are upregulated in gastric cancer tissues. Forced overexpression of FOXO6 promotes gastric cancer cell proliferation, while knockdown of FOXO6 expression inhibits proliferation. We show that ectopic FOXO6 expression induces the expression of C-myc. Furthermore, we found that FOXO6 physically interacts with the transcription factor hepatic nuclear factor 4 (HNF4) in gastric cancer cells. FOXO6 induces C-myc expression by associating to HNF4 and mediating histone acetylation, and the dissociation of HDAC3 from the promoter of the C-myc gene. Therefore, our results suggest a previously unknown FOXO6/HNF4/C-myc molecular network controlling gastric cancer development.

MeSH terms

  • Acetylation
  • Binding Sites
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Transformation, Neoplastic
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism*
  • Hepatocyte Nuclear Factor 4 / metabolism
  • Histone Deacetylases / metabolism
  • Histones / metabolism
  • Humans
  • Promoter Regions, Genetic
  • Protein Processing, Post-Translational
  • Proto-Oncogene Proteins c-myc / genetics
  • Proto-Oncogene Proteins c-myc / metabolism*
  • Stomach Neoplasms
  • Transcription, Genetic
  • Transcriptional Activation
  • Up-Regulation*

Substances

  • FOXO6 protein, human
  • Forkhead Transcription Factors
  • Hepatocyte Nuclear Factor 4
  • Histones
  • MYC protein, human
  • Proto-Oncogene Proteins c-myc
  • Histone Deacetylases
  • histone deacetylase 3