Journal
MOLECULAR ONCOLOGY
Volume 4, Issue 1, Pages 38-51Publisher
WILEY
DOI: 10.1016/j.molonc.2009.09.003
Keywords
Topoisomerase II; Etoposide; Double-stranded DNA breaks; Non-homologous end joining
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Funding
- Canadian Institutes of Health Research [MOP-13412]
- National Cancer Institute of Canada
- University of Ottawa
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Cytotoxicity of the topoisomerase II (topoII) poison etoposide has been ascribed to the persistent covalent trapping of topoII in DNA cleavage complexes that become lethal as cells replicate their DNA. However, short term etoposide treatment also leads to subsequent cell death, suggesting that the lesions that lead to cytotoxicity arise rapidly and prior to the onset DNA replication. In the present study 1 h treatment with 25 mu M etoposide was highly toxic and initiated a double-stranded DNA damage response as reflected by the recruitment of ATM, MDC1 and DNA-PKcs to gamma H2AX foci. While most DNA breaks were rapidly repaired upon withdrawal of the etoposide treatment, the repair machinery remained engaged in foci for at least 24 h following withdrawal. TopoII siRNA ablation showed the etoposide toxicity and gamma H2AX response to correlate with the inability of the cell to correct topoII alpha-initiated DNA damage. gamma H2AX induction was resistant to the inhibition of DNA replication and transcription, but was increased by pre-treatment with the histone deacetylase inhibitor trichostatin A. These results link the lethality of etoposide to the generation of persistent topoII alpha-dependent DNA defects within topologically open chromatin domains. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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