DNA Cleavage by the Antitumor Agent 3-Amino-1,2,4-benzotriazine 1,4-Dioxide (SR4233):  Evidence for Involvement of Hydroxyl Radical

Abstract

3-Amino-1,2,4-benzotriazine 1,4-dioxide (SR4233, WIN59075, tirapazamine, 1 ) is a clinically promising antitumor agent that requires bioreductive activation, selectively kills oxygen-deficient cells, and is believed to derive its biological activity from DNA cleavage. Using a xanthine−xanthine oxidase enzyme system as a one-electron reductant to activate 1 for DNA cleavage, it has been found that radical scavengers such as mannitol, dimethyl sulfoxide, ethanol, methanol, and tert -butyl alcohol significantly inhibit drug-dependent DNA cleavage. Compound 1, in concert with the xanthine−xanthine oxidase system, converts DMSO to methanesulfinic acid, a reaction characteristic of hydroxyl radical. In addition, treatment of a 32 P-labeled restriction fragment with reductively-activated 1 results in cleavage at every base pair, with little sequence specificity, consistent with involvement of a highly reactive, nonselective agent such as hydroxyl radical. These results strongly support the involvement of radicals in the cleavage of DNA by 1 and are consistent with hydroxyl radical as the major DNA-cleaving species generated by reduction of 1 .