AuthorsLusthof, K J
De Mol, N J
Janssen, L H
Hoey, Brigid M
Reinhoudt, David N
AffiliationDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Utrecht University, Sorbonnelaan, The Netherlands.
MetadataShow full item record
AbstractThe formation of reactive oxygen intermediates (ROI) during redox cycling of newly synthesized potential antitumor 2,5-bis (1-aziridinyl)-1,4-benzoquinone (BABQ) derivatives has been studied by assaying the production of ROI (superoxide, hydroxyl radical, and hydrogen peroxide) by xanthine oxidase in the presence of BABQ derivatives. At low concentrations (< 10 microM) some BABQ derivatives turned out to inhibit the production of superoxide and hydroxyl radicals by xanthine oxidase, while the effect on the xanthine-oxidase-induced production of hydrogen peroxide was much less pronounced. Induction of DNA strand breaks by reactive oxygen species generated by xanthine oxidase was also inhibited by BABQ derivatives. The DNA damage was comparable to the amount of hydroxyl radicals produced. The inhibiting effect on hydroxyl radical production can be explained as a consequence of the lowered level of superoxide, which disrupts the Haber-Weiss reaction sequence. The inhibitory effect of BABQ derivatives on superoxide formation correlated with their one-electron reduction potentials: BABQ derivatives with a high reduction potential scavenge superoxide anion radicals produced by xanthine oxidase, leading to reduced BABQ species and production of hydrogen peroxide from reoxidation of reduced BABQ. This study, using a unique series of BABQ derivatives with an extended range of reduction potentials, demonstrates that the formation of superoxide and hydroxyl radicals by bioreductively activated antitumor quinones can in principle be uncoupled from alkylating activity.
CitationRedox cycling of potential antitumor aziridinyl quinones. 1992, 13 (6):599-608 Free Radic. Biol. Med.
JournalFree Radical Biology & Medicine
- Reductive activation of potential antitumor bis(aziridinyl)benzoquinones by xanthine oxidase: competition between oxygen reduction and quinone reduction.
- Authors: Lusthof KJ, Richter W, de Mol NJ, Janssen LH, Verboom W, Reinhoudt DN
- Issue date: 1990 Feb 15
- Interactions between potential anti-tumour 2,5-bis(1-aziridinyl)-1,4-benzoquinone derivatives and glutathione: reductive activation, conjugation and DNA damage.
- Authors: Lusthof KJ, de Mol NJ, Janssen LH, Prins B, Verboom W, Reinhoudt DN
- Issue date: 1990 Aug
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- Issue date: 1992 Dec
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