The cytotoxicity of N3-methyl-5%-deoxy-5-fluorouridine (N3-Me-5%-dFUR), a novel metabolite of the anticancer pro-drug 5%-deoxy-5-fluorouridine (5%-dFUR), has been evaluated by in vitro experiments with cultures of different cancer cell lines. The new metabolic product was found to be non-toxic in all the cell growth experiments performed. The absence of cytotoxicity could be explained by the observation that the metabolite was not recognized as a substrate by thymidine phosphorilase, the enzyme responsible for 5-fluorouracil (5-FU) release from doxifluridine, as ascertained by high-performance liquid chromatography:ultraviolet (HPLC–UV) analysis of the incubation mixture. The biomethylation process leading to N3-Me-5%-dFUR could be considered as a possible detoxification pathway, altering the drug bioavailability, in competition with 5%-dFUR cleavage to the active 5-FU.

In vitro toxicity of N3-Methyl-5’-deoxy-5-fluorouridine, a novel metabolite of doxifluridine: a bioanalytical investigation

ZAMBONIN, Carlo;ARESTA, Antonella Maria;GRANO, Maria
1998-01-01

Abstract

The cytotoxicity of N3-methyl-5%-deoxy-5-fluorouridine (N3-Me-5%-dFUR), a novel metabolite of the anticancer pro-drug 5%-deoxy-5-fluorouridine (5%-dFUR), has been evaluated by in vitro experiments with cultures of different cancer cell lines. The new metabolic product was found to be non-toxic in all the cell growth experiments performed. The absence of cytotoxicity could be explained by the observation that the metabolite was not recognized as a substrate by thymidine phosphorilase, the enzyme responsible for 5-fluorouracil (5-FU) release from doxifluridine, as ascertained by high-performance liquid chromatography:ultraviolet (HPLC–UV) analysis of the incubation mixture. The biomethylation process leading to N3-Me-5%-dFUR could be considered as a possible detoxification pathway, altering the drug bioavailability, in competition with 5%-dFUR cleavage to the active 5-FU.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/129228
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