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[Cancer Research 55, 3352-3356, August 1, 1995]
© 1995 American Association for Cancer Research

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2-Amino-6-methoxypurine Arabinoside: An Agent for T-Cell Malignancies

Catherine U. Lambe1, Devron R. Averett, Melanie T. Paff, John E. Reardon, Joan G. Wilson and Thomas A. Krenitsky

Wellcome Research Laboratories, Research Triangle Park, North Carolina 27709

Earlier studies have shown guanine arabinoside (ara-G) is an effective agent against growth of T-cell lines and freshly isolated human T-leukemic cells. However, poor water solubility of ara-G limits clinical use. 2-Amino-6-methoxypurine arabinoside (506U) is a water-soluble prodrug converted to ara-G by adenosine deaminase. 506U is not a substrate for deoxycytidine kinase, adenosine kinase, or purine nucleoside phosphorylase and is phosphorylated by mitochondrial deoxyguanosine kinase at a rate 4% that of ara-G phosphorylation. Mitochondrial DNA polymerase was the least sensitive to ara-GTP inhibition of the five human DNA polymerases tested. [3H]506U was anabolized to ara-G 5'-phosphates in CEM cells but not to phosphorylated metabolites of 506U. 506U was selective for transformed T over B cells and also inhibited growth in two of three monocytic lines tested. 506U given i.v. to cynomolgus monkeys was rapidly converted to ara-G; the ara-G had a half-life of approximately 2 h. 506U had in vivo dose-dependent efficacy against human T-cell tumors in immunodeficient mice. A Phase 1 trial of 506U against refractory hematological malignancies is now in progress at two study sites.

1 To whom requests for reprints should be addressed, at Wellcome Research Laboratories, 3030 Cornwallis Road, Research Triangle Park, NC 27709.

Received 3/ 9/95. Accepted 5/26/95.




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Copyright © 1995 by the American Association for Cancer Research.