CCAAT/enhancer-binding protein delta mediates tumor necrosis factor alpha-induced Aurora kinase C transcription and promotes genomic instability

J Biol Chem. 2011 Aug 19;286(33):28662-28670. doi: 10.1074/jbc.M111.270710. Epub 2011 Jun 28.

Abstract

Epidemiologic and clinical research indicates that chronic inflammation increases the risk of certain cancers, possibly through chromosomal instability. However, the mechanism of inflammation-dependent chromosomal instability associated with tumorigenesis is not well characterized. The transcription factor CCAAT/enhancer-binding protein δ (C/EBPδ, CEBPD) is induced by tumor necrosis factor α (TNFα) and expressed in chronically inflamed tissue. In this study, we show that TNFα promotes aneuploidy. Loss of CEBPD attenuated TNFα-induced aneuploidy, and CEBPD caused centromere abnormality. Additionally, TNFα-induced CEBPD expression augmented anchorage-independent growth. We found that TNFα induced expression of aurora kinase C (AURKC) through CEBPD, and that AURKC also causes aneuploidy. Furthermore, high CEBPD expression correlated with AURKC expression in inflamed cervical tissue specimens. These data provide insight into a novel function for CEBPD in inducing genomic instability through the activation of AURKC expression in response to inflammatory signals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aneuploidy
  • Animals
  • Aurora Kinase C
  • Aurora Kinases
  • CCAAT-Enhancer-Binding Protein-delta / genetics
  • CCAAT-Enhancer-Binding Protein-delta / metabolism*
  • Centromere / genetics
  • Centromere / metabolism
  • Centromere / pathology
  • Cervix Uteri / metabolism*
  • Cervix Uteri / pathology
  • Female
  • Gene Expression Regulation, Enzymologic / drug effects
  • Gene Expression Regulation, Enzymologic / genetics
  • Genomic Instability*
  • HeLa Cells
  • Humans
  • Mice
  • Mice, Knockout
  • Protein Serine-Threonine Kinases / biosynthesis*
  • Protein Serine-Threonine Kinases / genetics
  • Transcription, Genetic*
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology
  • Uterine Cervicitis / genetics
  • Uterine Cervicitis / metabolism*
  • Uterine Cervicitis / pathology

Substances

  • CEBPD protein, human
  • Cebpd protein, mouse
  • Tumor Necrosis Factor-alpha
  • CCAAT-Enhancer-Binding Protein-delta
  • AURKC protein, human
  • Aurkc protein, mouse
  • Aurora Kinase C
  • Aurora Kinases
  • Protein Serine-Threonine Kinases