Inhibition of cell growth of human hepatoma cell line (Hep G2) by a farnesyl protein transferase inhibitor: a preferential suppression of ras farnesylation

Int J Cancer. 1996 Mar 1;65(5):620-6. doi: 10.1002/(SICI)1097-0215(19960301)65:5<620::AID-IJC11>3.0.CO;2-B.

Abstract

So far, treatment with anti-cancer agents has failed to achieve satisfactory results in hepatocellular carcinoma. In the process of hepatocarcinogenesis, ras has been shown to play a role. ras requires a farnesyl moiety for activation. It has been found that UCFI-C (manumycin), an antibiotic, inhibits farnesyl protein transferase, an enzyme that catalyzes farnesylation. Therefore, we investigated the effects of UCFI-C on cell growth, prenylation of cellular proteins including ras and Rapl, MAP kinase activity, activities of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, and synthesis of cholesterol in a ras-activated human hepatoma cell line, Hep G2. Treatment with varying concentrations of UCF1-C(10-30 microM for 24 and 72 hr resulted in a time- and dose-dependent inhibition of cell numbers. 3H-Thymidine incorporation was also inhibited in a dose-dependent manner, with 50% inhibition after 44 hr being observed at a concentration of 17 microM. UCFI-C dose-dependently inhibited ras farnesylation and MAP kinase activity, but did not decrease Rap 1++ geranylgeranylation or prenylation of 21-to 26-kDa proteins. Neither the activities of 3-hydroxy-3-methylglutaryl-coenzyme A reductase nor cholesterol synthesis were inhibited. These results suggest that UCFI-C antagonizes the growth of Hep G2 via the suppression of ras farnesylation and could be a lead for the development of new anti-cancer agents blocking the function of oncogenic ras associated with human cancer, including hepatocellular carcinoma.

MeSH terms

  • Alkyl and Aryl Transferases*
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Carcinoma, Hepatocellular / pathology*
  • Cell Division / drug effects
  • Cholesterol / blood
  • GTP-Binding Proteins / metabolism
  • Humans
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Polyenes / pharmacology*
  • Polyunsaturated Alkamides
  • Transferases / antagonists & inhibitors*
  • Tumor Cells, Cultured
  • rap GTP-Binding Proteins

Substances

  • Polyenes
  • Polyunsaturated Alkamides
  • Cholesterol
  • Hydroxymethylglutaryl CoA Reductases
  • Transferases
  • Alkyl and Aryl Transferases
  • p21(ras) farnesyl-protein transferase
  • Calcium-Calmodulin-Dependent Protein Kinases
  • GTP-Binding Proteins
  • rap GTP-Binding Proteins
  • manumycin