Thioguanine substitution alters DNA cleavage mediated by topoisomerase II

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Abstract
Thiopurines and topoisomerase II-tar- geted drugs (e.g., etoposide) are widely used antican- cer drugs. However, topoisomerase II-targeted drugs can cause acute myeloid leukemia, with the risk of this secondary leukemia linked to a genetic defect in thio- purine catabolism. Chronic thiopurines result in thio- guanine substitution in DNA. The effect of these substitutions on DNA topoisomerase II activity is not known. Our goal was to determine whether deoxythio- guanosine substitution alters DNA cleavage stabilized by human topoisomerase II. We studied four variations of a 40 mer oligonucleotide with a topoisomerase II cleavage site, each with a single deoxythioguanosine in a different position relative to the cleavage site (2 1o r 12 in the top and 1 2o r14 in the bottom strand). Deoxythioguanosine substitution caused position-de- pendent quantitative effects on cleavage. With the 21 or 12 top and 1 2o r14 bottom substitutions, mean topoisomerase II-induced cleavage was 0.6-, 2.0-, 1.1-, and 3.3-fold that with the wild-type substrate (P50.011, < 0.008, 0.51, and < 0.001, respectively). In the presence of 100 mM etoposide, cleavage was enhanced for wild-type and all thioguanosine-modified substrates relative to no etoposide, with the 14 bottom substitu- tion showing greater etoposide-induced cleavage than the wild-type substrate (P50.015). We conclude that thioguanine incorporation alters the DNA cleavage induced by topoisomerase II in the presence and absence of etoposide, providing new insights to the mechanism of thiopurine effect and on the leukemo- genesis of thiopurines, with or without topoisomerase inhibitors.—Krynetskaia, N. F., Cai, X., Nitiss, J. L., Krynetski, E. Y., Relling, M. V. Thioguanine substitu- tion alters DNA cleavage mediated by topoisomerase II. FASEB J. 14, 2339-2344 (2000)
Funding Information
  • National Institutes of Health (CA51001, CA36401, CA52814, CA82313)
  • American Lebanese Syrian Associated Charities