CuZnSOD deficiency leads to persistent and widespread oxidative damage and hepatocarcinogenesis later in life

Sailaja Elchuri, Terry D. Oberley, Wenbo Qi, Richard S. Eisenstein, L. Jackson Roberts, Holly Van Remmen, Charles J. Epstein, Ting Ting Huang

Research output: Contribution to journalArticlepeer-review

477 Scopus citations


Mice deficient in CuZn superoxide dismutase (CuZnSOD) showed no overt abnormalities during development and early adulthood, but had a reduced lifespan and increased incidence of neoplastic changes in the liver. Greater than 70% of Sod1-/- mice developed liver nodules that were either nodular hyperplasia or hepatocellular carcinoma (HCC). Cross-sectional studies with livers collected from Sod1-/- and age-matched +/+ controls revealed extensive oxidative damage in the cytoplasm and, to a lesser extent, in the nucleus and mitochondria from as early as 3 months of age. A marked reduction in cytosolic aconitase, increased levels of 8-oxo dG and F2-isoprostanes, and a moderate reduction in glutathione peroxidase activities and porin levels were observed in all age groups of Sod1-/- mice examined. There were also age-related reductions in Mn superoxide dismutase activities and carbonic anhydrase III. Parallel to the biochemical changes, there were progressive increases in the DNA repair enzyme APEX1, the cell cycle control proteins cyclin D1 and D3, and the hepatocyte growth factor receptor Met. Increased cell proliferation in the presence of persistent oxidative damage to macromolecules likely contributes to hepatocarcinogenesis later in life.

Original languageEnglish (US)
Pages (from-to)367-380
Number of pages14
Issue number3
StatePublished - Jan 13 2005
Externally publishedYes


  • 8-oxo dG
  • APEX1
  • Aconitase
  • CuZnSOD
  • Cyclin D1
  • Hepatocellular carcinoma
  • Met

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research


Dive into the research topics of 'CuZnSOD deficiency leads to persistent and widespread oxidative damage and hepatocarcinogenesis later in life'. Together they form a unique fingerprint.

Cite this