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- Title
Sensitization of ara-C-resistant lymphoma cells by a pronucleotide analogue.
- Authors
Carlos María Galmarini; Marilyn L. Clarke; Cheryl L. Santos; Lars Jordheim; Christian Perigaud; Gilles Gosselin; Emeline Cros; John R. Mackey; Charles Dumontet
- Abstract
Adequate intracellular concentrations of ara-CMP, the monophosphorylated derivative of ara-C, are essential for its cytotoxicity. The critical step for ara-CMP formation is intracellular phosphorylation of ara-C by deoxycytidine kinase (dCK). A common nucleoside resistance mechanism is mutation affecting the expression or the specificity of dCK. We describe the ability of a tert-butyl S-acyl-thioethyl (SATE) derivative of ara-CMP (UA911) to circumvent ara-C resistance in a dCK-deficient human follicular lymphoma cell line (RL-G). The RL-G cell line was produced by continuous exposure to gemcitabine and displayed low dCK mRNA and protein expression that conferred resistance both to ara-C (2,250-fold) and to gemcitabine (2,092-fold). RL-G cells were able to take up the UA911 pronucleotide by diffusion and metabolize it to the corresponding ara-CMP and ara-CTP nucleotides, exhibiting a 199-fold reduction in resistance ratios, and a similar cell cycle arrest to the parental RL-7 cells. Exposures to 10, 50 or 100 μM concentrations of UA911 produced 160 ± 7, 269 ± 8 and 318 ± 62 pmol ara-CTP/mg protein in RL-7 cells, and 100 ± 12, 168 ± 10 and 217 ± 39 pmol ara-CTP/mg protein in RL-G cells, respectively. Exposure of RL-G cells to underivatized, radiolabeled ara-C produced no detectable amounts of the active triphosphate metabolites. We conclude that the UA911 pronucleotide is capable of overcoming dCK-mediated resistance. This result can be attributed to the unique cellular metabolism of the SATE pronucleotides giving rise to the intracellular delivery of ara-CMP to dCK-deficient cells. © 2003 Wiley-Liss, Inc.
- Subjects
CELL-mediated cytotoxicity; PHOSPHORYLATION; NUCLEOSIDES; LYMPHOMAS
- Publication
International Journal of Cancer, 2003, Vol 107, Issue 1, p149
- ISSN
0020-7136
- Publication type
Article
- DOI
10.1002/ijc.11339