Inhibition of intracellular bleomycin hydrolase activity by E-64 leads to the potentiation of the cytotoxicity of peplomycin against Chinese hamster lung cells

Jpn J Cancer Res. 1989 Jan;80(1):65-8. doi: 10.1111/j.1349-7006.1989.tb02246.x.

Abstract

N-(N-(L-3-trans-carboxyoxiran-2-carbonyl)-L-leucyl)-agmatine (E-64), a thiol protease inhibitor, potentiated the cytotoxicity of peplomycin against the Chinese hamster lung (V79) cell. After the treatment of the cells with E-64 (50 micrograms/ml) for 12 h, bleomycin hydrolase activity of the cells was almost completely inhibited. V79 cells treated with [3H]peplomycin for 24 h in the presence of E-64 (50 micrograms/ml) accumulated twice as much [3H]peplomycin and five times less [3H]desamidopeplomycin compared with V79 cells treated in the absence of E-64. These results suggest that E-64 increases the sensitivity of V79 cells to peplomycin probably by inhibiting the intracellular bleomycin hydrolase activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bleomycin / metabolism
  • Bleomycin / pharmacology*
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cricetinae
  • Cricetulus
  • Cysteine Endopeptidases*
  • Drug Synergism
  • Glycoside Hydrolases / antagonists & inhibitors*
  • Leucine / analogs & derivatives*
  • Leucine / pharmacology
  • Lung / drug effects
  • Peplomycin
  • Protease Inhibitors / pharmacology*

Substances

  • Protease Inhibitors
  • Bleomycin
  • Peplomycin
  • Glycoside Hydrolases
  • Cysteine Endopeptidases
  • bleomycin hydrolase
  • Leucine
  • E 64