Inhibition of rat liver regeneration after partial hepatectomy and induction of ERK phosphorylation by Cpd 5, a K vitamin-based anticancer compound.

Abstract

Thioalkyl K vitamin derivatives, like 2-(2-mercaptoethanol)-3-methyl-1,4-naphthoquinone (Cpd 5), have been shown to inhibit both hepatoma cell growth and DNA synthesis in rat hepatocytes in vitro. We have here examined the tissue distribution, in vivo tolerance and growth inhibitory effects of a single injected dose of Cpd 5 in rats. Cpd 5 administered i.p. was sufficient to cause a 90% inhibition of the peak in DNA synthesis in rat liver 24 h after two-thirds partial hepatectomy (PH). However, DNA synthesis in post-PH, Cpd 5-treated rat livers did occur, but with a delay of 36 h. Dual phosphorylation of ERK2 was induced in rat liver dose-dependently as early as 0.5 h, but gradually returned to almost basal levels by 6 h after Cpd 5 treatment. The MEK1/2 inhibitor PD098059, administered in vivo 1 h prior to Cpd 5 treatment, antagonized both induction of ERK2 phosphorylation and inhibition of DNA synthesis in rat liver. Liver protein lysates post-PH exhibited protein phosphatase activity for phospho-ERK2, which was inhibited by Cpd 5. These results show that induction of ERK2 phosphorylation is likely involved in the mechanism by which Cpd 5 inhibits PH-induced DNA synthesis, probably as a result of its ability to inhibit the activity of ERK phosphatase(s).

• Authors: Siddhartha Kar, Meifang Wang, Kathryn S Rosi, Craig S Wilcox, Brian I Carr
• Journal: Carcinogenesis (Carcinogenesis) Vol. 25 Issue 12 Pg. 2345-51 (Dec 2004) ISSN: 0143-3334 [Print] England
• PMID: 15319298 (Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• 2-(2-hydroxyethylsulfanyl)-3-methyl-1,4-naphthoquinone
• Antineoplastic Agents
• Enzyme Inhibitors
• Vitamin K
• DNA
• Mitogen-Activated Protein Kinase 1
• Mitogen-Activated Protein Kinase 3

Topics

• Animals
• Antineoplastic Agents (pharmacology)
• DNA (antagonists & inhibitors, genetics, metabolism)
• Enzyme Inhibitors (pharmacology)
• Hepatectomy
• Liver Regeneration (drug effects)
• Male
• Mitogen-Activated Protein Kinase 1 (antagonists & inhibitors, metabolism)
• Mitogen-Activated Protein Kinase 3 (metabolism)
• Phosphorylation (drug effects)
• Rats
• Rats, Inbred F344
• Tissue Distribution
• Vitamin K (analogs & derivatives, pharmacology)