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Therapy of Mouse Leukemia L1210 with Combinations of Nebularine and Nitrobenzylthioinosine 5'-Monophosphate¹

Cancer Research Unit (McEachern Laboratory), University of Alberta, Edmonton, Alberta, Canada T6G 2H7

ABASTRACT: Earlier reports from this laboratory showed that: (a) in the presence of nitrobenzylthioinosine (NBMPR), a potent, tightly bound inhibitor of nucleoside transport, cells proliferating in culture were protected against a number of cytotoxic nucleosides; and (b) mice were protected against potentially lethal dosages of nebularine (and other toxic nucleosides) by coad-ministration of NBMPR. The present study, which used nitro-benzylthioinosine 5'-phosphate (NBMPR-P), a readily soluble "prodrug" form of NBMPR, extended the in vivo protection studies and showed that the half-life of the protection effect was about 4 hr. In chemotherapy experiments, mice bearing transplanted neoplasms were treated with high dosages of nebularine together with protecting doses of NBMPR-P. When mice bearing leukemia L1210 were treated with a potentially lethal regimen of nebularine administered together with NBMPR-P, a substantial kill of leukemic cells resulted (some mice were long-term survivors). The therapeutic effect was optimal at dosage levels of the protecting agent in excess of those required in nonleukemic mice for protection against the lethal nebularine dosages used, suggesting that the therapeutic effect was due to the joint presence in the leukemic cells of a metabolite of NBMPR-P and nebularine; NBMPR-P protection of the leukemic host against nebularine lethality was necessary for the therapeutic effect to be manifested.

¹ Supported by the National Cancer Institute of Canada. A portion of this work was described in a preliminary communication (19).

² To whom requests for reprints should be addressed.

Received 6/30/80. Accepted 10/22/80.

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