Topoisomerase II inhibition by the bioactivated benzene metabolite hydroquinone involves multiple mechanisms.

While benzene is widely recognized as a human and animal carcinogen, the key mechanisms underlying its carcinogenic effects remain unknown. Inhibition of topoisomerase II (topoII) by benzene and its metabolites represents a potential mechanism by which benzene could induce its chromosome-altering and leukemogenic effects. Previous work from our laboratory and others has demonstrated that bioactive benzene metabolites are capable of inhibiting topoII in isolated enzyme and cell culture systems. Similarly, a decrease in topoII activity has been seen in the bone marrow of mice administered benzene in vivo. The objective of these studies was to further investigate the mechanisms by which the bioactivated benzene metabolite, hydroquinone (BAHQ), inhibits topoII in vitro, and to identify the point(s) in the enzyme's catalytic cycle where inhibition occurs. Our experiments indicate that BAHQ inhibits topoII at the DNA binding stage as well as in the closed clamp stage in the catalytic cycle, thereby interfering with either the binding to, or the release of, DNA from the enzyme. While increases in the cleavable complex were also seen with BAHQ treatment, our results suggest that this is related to a shift in equilibrium due to an accumulation of the topoII enzyme at the closed clamp stage rather than a major inhibitory effect on the religation step. An increase in cleavable complex formation as well as the inhibition of enzymatic activity at the closed clamp and other stages of the catalytic cycle in bone marrow cells would likely result in DNA breakage, the formation of chromosomal aberrations, and could potentially result in leukemia-associated chromosomal translocations, similar to those seen in leukemias induced by the bisdioxopiperazine type of catalytic topoII inhibitors. Copyright (c) 2009 Elsevier Ireland Ltd. All rights reserved.