Loss of the nucleosome-binding protein HMGN1 affects the rate of N-nitrosodiethylamine-induced hepatocarcinogenesis in mice

Mol Cancer Res. 2014 Jan;12(1):82-90. doi: 10.1158/1541-7786.MCR-13-0392. Epub 2013 Dec 2.

Abstract

We report that HMGN1, a nucleosome-binding protein that affects chromatin structure and function, affects the growth of N-nitrosodiethylamine (DEN)-induced liver tumors. Following a single DEN injection at 2 weeks of age, Hmgn1(tm1/tm1) mice, lacking the nucleosome-binding domain of HMGN1, had earlier signs of liver tumorigenesis than their Hmgn1(+/+) littermates. Detailed gene expression profiling revealed significant differences between DEN-injected and control saline-injected mice, but only minor differences between the injected Hmgn1(tm1/tm1) mice and their Hmgn1(+/+) littermates. Pathway analysis revealed that the most significant process affected by loss of HMGN1 involves the lipid/sterol metabolic pathway. Our study indicates that in mice, loss of HMGN1 leads to transcription changes that accelerate the progression of DEN-induced hepatocarcinogenesis, without affecting the type of tumors or the final total tumor burden of these mice.

Implications: Loss of HMGN1 leads to accelerated progression of DEN-induced hepatocarcinogenesis in mice.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Cell Transformation, Neoplastic / genetics*
  • Chromatin / genetics
  • Diethylnitrosamine / pharmacology*
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic
  • HMGN1 Protein / genetics*
  • Lipid Metabolism / genetics*
  • Liver / pathology
  • Liver Neoplasms / chemically induced
  • Liver Neoplasms / genetics*
  • Mice
  • Mice, Knockout
  • Tumor Burden

Substances

  • Chromatin
  • HMGN1 Protein
  • Diethylnitrosamine