British Journal of Cancer (2000) 83, 1740–1746. doi:10.1054/bjoc.2000.1514 www.bjcancer.com
Published online 5 December 2000
Characterization of DNA-strand breakage induced in V79 cells by F 11782, a catalytic inhibitor of topoisomerases
J-M Barret1, B T Hill1 and P L Olive2
- 1Division de Cancérologie, Centre de RecherchePierre Fabre, 17 avenue Jean Moulin, Castres, 81100, France
- 2Medical Biophysics Department, British Columbia Cancer Research Centre, Vancouver, V5Z IL3, Canada
Received 31 March 2000; Revised 7 August 2000; Accepted 13 August 2000.
Top of pageAbstract
DNA damage induced in V79 cells by F 11782, or 2",3"-bis pentafluorophenoxyacetyl-4',
6'-ethylidene-
-D glucoside of 4'-phosphate-
4'-demethylepipodophyllotoxin 2N-methyl glucamine salt, a novel dual catalytic inhibitor of topoisomerases I and II, was investigated using both alkaline and neutral versions of the comet assay methodology. A comparison was then made of the DNA damage induced by F 11782 with that induced by either etoposide or camptothecin under comparable experimental conditions. The results revealed that F 11782 initially induced less DNA strand breaks that either etoposide or camptothecin and rejoined such breaks more slowly. However, unlike these other drugs, the extent of DNA damage induced by F 11782 increased linearly with time of incubation. F 11782 produced both DNA single- and double-strand breaks without any clear specificity relative to phase of the cell cycle, although proliferating cells were preferentially damaged. The marked time-dependency of induction of DNA strand breaks by F 11782 may serve to explain, at least in part, its major in vivo antitumour activities. © 2000 Cancer Research Campaign http://www.bjcancer.com
Keywords:
F 11782, catalytic topoisomerase inhibitor, DNA-strand breaks, comet assay
Top of pageReferences
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