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脱氧尿苷一磷酸(dUMP)和游离氟脱氧尿苷一磷酸(FdUMP)池与5-氟尿嘧啶对胸苷酸合成酶抑制作用的关系

Relationship of dUMP and free FdUMP pools to inhibition of thymidylate synthase by 5-fluorouracil.

作者信息

Berger S H, Hakala M T

出版信息

Mol Pharmacol. 1984 Mar;25(2):303-9.

PMID:6608049
Abstract

The purpose of this study was to compare the pools of free FdUMP derived from 5-fluorouracil (FUra) and of dUMP synthesized de novo in Hep-2 and S-180 cells, their relationship to inhibition of thymidylate synthase (dTMP synthase; EC 2.1.1.45), and the effect of excess folinic acid (CF) on these parameters. These cells differ 50-fold in their sensitivity to FUra and, in the absence of thymidine, dTMP synthase is the growth-limiting site of action of FUra in S-180 cells, but in Hep-2 cells this site becomes growth-limiting only in the presence of excess folates. In both cells after a 3-hr incubation with varied concentrations of FUra, FdUMP comprised only 0.1-0.2% of the total acid-soluble pools derived from FUra. The changes in dUMP and FdUMP pools paralleled each other, dUMP being 1000-2000 times higher than FdUMP. The pools of dUMP increased only when dTMP synthase was significantly inhibited. This occurred in S-180 cells above 3 microM FUra and in Hep-2 cells above 30 microM, where the residual dTMP synthase was similar in both cells. Under these conditions, the dUMP and FdUMP pools in Hep-2 cells were 2 and 4 times higher, respectively, than in S-180 cells. After FUra removal, both pools continued to increase, dUMP and FdUMP pools in Hep-2 cells rising 6-fold and 10-fold higher, respectively, than in S-180 cells. The dTMP synthase inhibition and the high nucleotide pools in Hep-2 were short-lived, whereas in S-180 cells the inhibition and the pools were maintained longer. Excess CF retarded the recovery of dTMP synthase after FUra removal only in Hep-2 cells and led to a further increase in dUMP and FdUMP pools in these cells, while having no effect in S-180 cells. These data indicate that a high capacity of cells to accumulate free FdUMP does not alone guarantee that dTMP synthase inhibition will be growth-limiting. The relationship shown here between excess CF, dTMP synthase recovery, and the nucleotide pools suggests that some cell types, such as Hep-2, in spite of high levels of FdUMP, require in addition an excess of folates to retard dTMP synthase recovery and make it growth-limiting.

摘要

本研究的目的是比较在Hep-2细胞和S-180细胞中,由5-氟尿嘧啶(FUra)衍生而来的游离FdUMP池以及从头合成的dUMP池,它们与胸苷酸合成酶(dTMP合成酶;EC 2.1.1.45)抑制作用的关系,以及过量亚叶酸(CF)对这些参数的影响。这些细胞对FUra的敏感性相差50倍,并且在无胸苷的情况下,dTMP合成酶是FUra在S-180细胞中作用的生长限制位点,但在Hep-2细胞中,仅在存在过量叶酸时该位点才成为生长限制位点。在两种细胞中,用不同浓度的FUra孵育3小时后,FdUMP仅占源自FUra的总酸溶性池的0.1 - 0.2%。dUMP和FdUMP池的变化相互平行,dUMP比FdUMP高1000 - 2000倍。仅当dTMP合成酶受到显著抑制时,dUMP池才会增加。这在S-180细胞中发生在FUra浓度高于3 microM时,在Hep-2细胞中发生在高于30 microM时,此时两种细胞中残余的dTMP合成酶相似。在这些条件下,Hep-2细胞中的dUMP和FdUMP池分别比S-180细胞高2倍和4倍。去除FUra后,两个池继续增加,Hep-2细胞中的dUMP和FdUMP池分别比S-180细胞升高6倍和10倍。Hep-2细胞中dTMP合成酶的抑制和高核苷酸池是短暂的,而在S-180细胞中,抑制作用和池维持的时间更长。过量的CF仅在Hep-2细胞中延缓了FUra去除后dTMP合成酶的恢复,并导致这些细胞中dUMP和FdUMP池进一步增加,而在S-180细胞中没有影响。这些数据表明,细胞积累游离FdUMP的高能力本身并不能保证dTMP合成酶的抑制将成为生长限制因素。此处显示的过量CF、dTMP合成酶恢复和核苷酸池之间的关系表明,某些细胞类型,如Hep-2细胞,尽管FdUMP水平很高,但还需要过量的叶酸来延缓dTMP合成酶的恢复并使其成为生长限制因素。

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