The DNA topoisomerase II catalytic inhibitor merbarone is genotoxic and induces endoreduplication

• Published in: Mutation research Vol. 738-739; p. 45
• Main Authors: Pastor, Nuria, Domínguez, Inmaculada, Orta, Manuel Luís, Campanella, Claudia, Mateos, Santiago, Cortés, Felipe
• Format: Journal Article
• Language: English
• Published: Netherlands 01-10-2012
• Subjects: Animals; Cell Line; Cell Proliferation - drug effects; Cricetinae; Cricetulus; DNA Damage - drug effects; Endoreduplication - drug effects; Thiobarbiturates - toxicity; Topoisomerase II Inhibitors - toxicity
• ISSN: 0027-5107
• DOI: 10.1016/j.mrfmmm.2012.07.005

In the last years a number of reports have shown that the so-called topoisomerase II (topo II) catalytic inhibitors are able to induce DNA and chromosome damage, an unexpected result taking into account that they do not stabilize topo II-DNA cleavable complexes, a feature of topo II poisons such as etoposide and amsacrine. Merbarone inhibits the catalytic activity of topo II by blocking DNA cleavage by the enzyme. While it was first reported that merbarone does not induce genotoxic effects in mammalian cells, this has been challenged by reports showing that the topo II inhibitor induces efficiently chromosome and DNA damage, and the question as to a possible behavior as a topo II poison has been put forward. Given these contradictory results, and the as yet incomplete knowledge of the molecular mechanism of action of merbarone, in the present study we have tried to further characterize the mechanism of action of merbarone on cell proliferation, cell cycle, as well as chromosome and DNA damage in cultured CHO cells. Merbarone was cytotoxic as well as genotoxic, inhibited topo II catalytic activity, and induced endoreduplication. We have also shown that merbarone-induced DNA damage depends upon ongoing DNA synthesis. Supporting this, inhibition of DNA synthesis causes reduction of DNA damage and increased cell survival.