Generation of free radicals from neocarzinostatin mediated by NADPH/cytochrome P-450 reductase via activation of enediyne chromophore

Biochem Biophys Res Commun. 1994 Dec 30;205(3):1716-23. doi: 10.1006/bbrc.1994.2866.

Abstract

Neocarzinostatin (NCS) is one of the most potent antitumor agents. It contains a chromophore of a unique enediyne structure as its prosthetic group. Here, we report the generation of free radicals from NCS by the NADPH/cytochrome (cyt) P-450 reductase system. Free radical species, which were generated in the reaction mixture of NCS/NADPH/cyt P-450 reductase, were identified by using electron spin resonance spin trapping with 5,5-dimethyl-1-pyrroline N-oxide (DMPO). The spin adducts of superoxide and hydroxyl radical (DMPO-OOH and DMPO-OH, respectively) were generated in the reaction of NCS with the NADPH/cyt P-450 reductase system. From kinetic analyses of DMPO-OOH generation as a function of the concentration of NCS, the Vmax/Km value of the reaction was 0.4 x 10(6) M-1min-1. In addition, we identified thiyl radical generation in this system in the presence of glutathione. These results indicate that NCS is a potent generator of free radicals in cells where cyt P-450 reductase is available. Moreover, it seems that free radicals, generated by enzymatic activation of NCS, are involved in cytotoxicity of NCS as well as in DNA damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cyclic N-Oxides
  • Electron Spin Resonance Spectroscopy
  • Free Radicals
  • In Vitro Techniques
  • Kinetics
  • Microsomes, Liver / enzymology
  • NADPH-Ferrihemoprotein Reductase / metabolism*
  • Rats
  • Reactive Oxygen Species / metabolism
  • Spin Labels
  • Zinostatin / chemistry
  • Zinostatin / metabolism*
  • Zinostatin / pharmacology

Substances

  • Cyclic N-Oxides
  • Free Radicals
  • Reactive Oxygen Species
  • Spin Labels
  • 5,5-dimethyl-1-pyrroline-1-oxide
  • Zinostatin
  • NADPH-Ferrihemoprotein Reductase