细胞外谷氨酰胺水平降低增强5-氟尿嘧啶细胞毒性。

Cancer biochemistry biophysics Pub Date : 1998-06-01
S Sukemori, K Sugimura
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引用次数: 0

摘要

将培养的P388(小鼠)和CEM(人)白血病细胞暴露于含有5-氟尿嘧啶(5-FU)或甲氧蝶呤(MTX)的培养基中。药物水平低于RPMI 1640培养基(对照)的ID50值。在将天冬酰胺或谷氨酰胺水平降低到对照水平的60%的培养基中,确定了药物细胞毒性的增强。两种类型的细胞增殖3天显示药物的细胞毒性。与对照相比,天冬酰胺还原培养基没有增强5-FU的细胞毒性,而谷氨酰胺还原培养基没有增强MTX的细胞毒性。细胞外谷氨酰胺水平的调节似乎影响细胞周期的G1期,正如先前阿霉素的结果所发现的那样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extracellular glutamine level reduction enhances 5-fluorouracil cytotoxicity.

Cultured P388 (murine) and CEM (human) leukemia cells were exposed to medium including either 5-fluorouracil (5-FU) or methotorexate (MTX). The level of drug was less than the ID50 value obtained in RPMI 1640 medium (control). Enhancement of drug cytotoxicity was determined with medium in which asparagine or glutamine level had been reduced to 60% of the level of the control. Proliferation of both types of cells for 3 days showed the cytotoxicities of the drugs. Asparagine reduced medium showed no enhancement of cytotoxicity in comparison with control, while glutamine reduced medium enhanced the cytotoxicity of 5-FU, but not that of MTX. Regulation of extracellular glutamine level seemed to affect stage G1 of the cell cycle, as found in the previous result with adriamycin.

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