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人白血病成髓细胞中三磷酸阿糖胞苷的产生:与脱氧胞苷的相互作用

Cytosine arabinoside triphosphate production in human leukaemic myeloblasts: interactions with deoxycytidine.

作者信息

Harris A L, Grahame-Smith D G

出版信息

Cancer Chemother Pharmacol. 1981;5(3):185-92. doi: 10.1007/BF00258478.

Abstract

The effect of 1 mu M deoxycytidine (dC) on Ara-C conversion to Ara-CTP and on inhibition of DNA synthesis by Ara-C was measured in intact leukaemic myeloblasts. dC decreased Ara-CTP production in blasts with high Ara-C phosphorylation, but not those with low activity. The Ki for dC was similar to values found with partially purified deoxycytidine kinase. The change in Ara-CTP concentration was associated with a proportional reduction in inhibition of DNA synthesis. dC decreased the effects of Ara-C by inhibition of Ara-CTP production, rather than by production of dCTP and competition with Ara-CTP. Since low Ara-CTP production in patients' blasts is a predictor of poor therapeutic response to Ara-C, the use of dC with Ara-C may improve the therapeutic index in this group of patients.

摘要

在完整的白血病原粒细胞中,测定了1μM脱氧胞苷(dC)对阿糖胞苷(Ara-C)转化为阿糖胞苷三磷酸(Ara-CTP)以及对Ara-C抑制DNA合成的影响。dC降低了Ara-C磷酸化水平高的原粒细胞中Ara-CTP的产生,但对活性低的原粒细胞没有影响。dC的半数抑制浓度(Ki)与用部分纯化的脱氧胞苷激酶测得的值相似。Ara-CTP浓度的变化与DNA合成抑制的成比例降低相关。dC通过抑制Ara-CTP的产生而降低了Ara-C的作用,而不是通过产生脱氧胞苷三磷酸(dCTP)并与Ara-CTP竞争。由于患者原粒细胞中Ara-CTP产生量低是对Ara-C治疗反应不佳的预测指标,因此将dC与Ara-C联合使用可能会提高这组患者的治疗指数。

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