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联合抗叶酸剂对体外培养的小鼠白血病细胞生长抑制的作用。

The effects of combined antifolates on inhibition of growth of murine leukemia cells cultured in vitro.

作者信息

Balińska M, Szablewska I, Janiszewska D, Bartuzi K, Pawełczak K

机构信息

M. Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw.

出版信息

Acta Biochim Pol. 1997;44(4):743-50.

PMID:9584854
Abstract

The synergistic effect of trimetrexate (TMTX) and sulphonamide derivatives of quinazoline on the cultured 5178Y murine leukemia cells was examined. On exposure to the slightly inhibitory concentrations of TMTX (0.1 nM) in combination with 2-desamino-2-methyl-10-propargyl-5,8-dideaza-pteroyl-sulphoglyc ine (DMPDDSF) (0.02 microM) a synergistic inhibitory effect of the antifolates on cell growth was observed. These two drugs in the same combination caused also synergistic inhibition of de novo synthesis of thymidylate in intact cells as measured by tritium release from [5-(3)H]deoxyuridylate. This was accompanied by a marked reduction in intracellular concentration of 5,10-methylenetetrahydro-pteroyl-polyglutamate (5,10CH2H4PteGlu(n)) (0.2 microM) and dihydropteroyl-polyglutamate (0.12 microM). In these conditions de novo biosynthesis of purine was decreased by 50%. These observations show that growth inhibition by combined antifolates is mediated by intracellular depletion of the substrate of thymidylate synthase -- 5,10CH2H4PteGlu(n). The results obtained strongly suggest that under certain conditions inhibition of thymidylate synthesis by DMPDDSF is intensified by prior application of TMTX -- an inhibitor of dihydrofolate reductase.

摘要

研究了三甲曲沙(TMTX)与喹唑啉磺酰胺衍生物对培养的5178Y小鼠白血病细胞的协同作用。当暴露于低抑制浓度的TMTX(0.1 nM)与2-脱氨基-2-甲基-10-炔丙基-5,8-二去氮蝶酰-磺基甘氨酸(DMPDDSF)(0.02 microM)的组合时,观察到抗叶酸剂对细胞生长具有协同抑制作用。相同组合的这两种药物对完整细胞中胸苷酸从头合成也有协同抑制作用,这通过[5-(3)H]脱氧尿苷酸的氚释放来测定。同时,细胞内5,10-亚甲基四氢蝶酰-多聚谷氨酸(5,10CH2H4PteGlu(n))(0.2 microM)和二氢蝶酰-多聚谷氨酸(0.12 microM)的浓度显著降低。在这些条件下,嘌呤的从头生物合成减少了50%。这些观察结果表明,联合抗叶酸剂的生长抑制作用是由胸苷酸合酶的底物——5,10CH2H4PteGlu(n)的细胞内耗竭介导的。所得结果强烈表明,在某些条件下,DMPDDSF对胸苷酸合成的抑制作用会因预先应用二氢叶酸还原酶抑制剂TMTX而增强。

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