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首页> 外文期刊>British Journal of Cancer >5-fluorouracil and 5-fluoro-2'-deoxyuridine follow different metabolic pathways in the induction of cell lethality in L1210 leukaemia
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5-fluorouracil and 5-fluoro-2'-deoxyuridine follow different metabolic pathways in the induction of cell lethality in L1210 leukaemia

机译:5-氟尿嘧啶和5-氟-2'-脱氧尿苷在诱导L1210白血病细胞致死性中遵循不同的代谢途径

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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.
机译:研究了5-氟尿嘧啶(FUra)和5-氟-2'-脱氧尿苷(FdUrd)对L1210白血病的作用方式。结果表明,FUra和FdUrd遵循不同的代谢途径,并具有不同的细胞毒活性靶标。 FUra被转化为5-氟尿苷-5'三磷酸(FUTP),并被整合到新生的RNA中。 FdUrd转化为5-氟-2'-脱氧尿苷-5'-单磷酸酯(FdUMP),从而抑制了2'-脱氧胸苷-5'-单磷酸酯(dTMP)的从头合成。确实发生了FUra向FdUMP的转化,但是这种现象并没有促进最终的细胞毒性作用。未检测到FdUrd到FUra的转换。

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