Changes in the antioxidant system by TNP-470 in an in vivo model of hepatocarcinoma

Transl Res. 2007 Sep;150(3):189-96. doi: 10.1016/j.trsl.2007.04.006. Epub 2007 May 21.

Abstract

The objective of this study was to determine in a rat model of hepatocarcinoma (HCC) the effects of the antiangiogenic agent TNP-470 on antioxidant enzymes, including catalase (CAT), superoxide dismutases (Mn-SOD and Cu,Zn-SOD), and glutathione peroxidase (GPx). Tumor was induced in male Wistar rats by diethylnitrosamine and promoted by two-thirds hepatectomy plus acetaminofluorene administration. Experiments were carried out 28 weeks after initiating the treatment. TNP-470 was administered at 30 mg/kg, 2 times per week from weeks 20 to 28. Carcinomatous tissue was growing outside dysplastic nodules in rats with HCC. HCC caused oxidative stress demonstrated by increased lipid peroxidation and oxidized/reduced glutathione ratio that was accompanied by a reduced activity of antioxidant enzymes Cu,Zn-SOD, GPx, and CAT. In contrast, Mn-SOD activity and expression were higher in hepatocarcinoma than in control groups. These effects were absent in animals receiving TNP-470. No significant differences between untreated and TNP-470-treated rats were observed in the expression of the Cu,Zn-SOD, glutathione peroxidise, and CAT. We conclude that TNP-470 inhibits expression and activity of Mn-SOD induced by experimental hepatocarcinogenesis. Oxidative stress reduction by TNP-470 accounts for yet another anti-cancer effect of this molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / pharmacology
  • Animals
  • Antioxidants / metabolism*
  • Carcinogens
  • Carcinoma, Hepatocellular / chemically induced
  • Carcinoma, Hepatocellular / drug therapy
  • Carcinoma, Hepatocellular / metabolism*
  • Cyclohexanes / pharmacology*
  • Diethylnitrosamine
  • Disease Models, Animal
  • Free Radical Scavengers / metabolism
  • Liver / metabolism*
  • Liver / pathology
  • Liver Neoplasms / chemically induced
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / metabolism*
  • Male
  • O-(Chloroacetylcarbamoyl)fumagillol
  • Oxidative Stress / drug effects*
  • Rats
  • Rats, Wistar
  • Sesquiterpenes / pharmacology*

Substances

  • Angiogenesis Inhibitors
  • Antioxidants
  • Carcinogens
  • Cyclohexanes
  • Free Radical Scavengers
  • Sesquiterpenes
  • Diethylnitrosamine
  • O-(Chloroacetylcarbamoyl)fumagillol