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Br J Cancer ; 49(6): 739-44, 1984 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-6234011

RESUMO

The mode of action of 5-fluorouracil (FUra) and 5-fluoro-2'-deoxyuridine (FdUrd) on L1210 leukaemia has been studied. It is shown that FUra and FdUrd follow different routes of metabolism and have different targets with respect to their cytotoxic activity. FUra is converted to 5-fluorouridine-5'triphosphate ( FUTP ), which is incorporated into nascent RNA. FdUrd is converted to 5-fluoro-2'-deoxyuridine-5'-monophosphate (FdUMP), which inhibits the de novo synthesis of 2'-deoxythymidine-5'-monophosphate (dTMP). Conversion of FUra to FdUMP does occur, but this phenomenon does not contribute to the final cytotoxic effect. No conversion of FdUrd to FUra has been detected.


Assuntos
Floxuridina/metabolismo , Fluoruracila/metabolismo , Leucemia L1210/metabolismo , Animais , Sobrevivência Celular/efeitos dos fármacos , Células Cultivadas , DNA de Neoplasias/metabolismo , Floxuridina/farmacologia , Fluoruracila/farmacologia , Isomerismo , Leucemia L1210/patologia , Timidina Monofosfato/metabolismo , Uridina Trifosfato/análogos & derivados , Uridina Trifosfato/metabolismo
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