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暴露于各种抗代谢物后L1210细胞糖基化的变化。

Changes in glycosylation of L1210 cells after exposure to various antimetabolites.

作者信息

De Graaf T W, Slot S S, Peters G J, Van Dijk W

机构信息

Department of Medical Chemistry, Faculty of Medicine, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

Eur J Cancer. 1993;29A(12):1760-5. doi: 10.1016/0959-8049(93)90120-5.

Abstract

This study establishes that antimetabolites do have the potency to change cellular glycosylation, as was suggested in our previous review (Eur J Cancer 1990, 26, 516-523). Murine leukaemia L1210 cells were exposed to various antimetabolites under non-lethal conditions. The antimetabolites 5-fluorouracil (5FU), arabinofuranosylcytosine (AraC), methotrexate (MTX) and 6-mercaptopurine (6MP), but not 6-thioguanine, induced considerable changes in the metabolic incorporation of radioactively labelled monosaccharides. Each antimetabolite exhibited a different effect. Significant differences were found between the radioactivity incorporated from the monosaccharides glucosamine, fucose, mannose and galactose, relative to control values. Polyacrylamide gel electrophoresis indicated that changes were induced in the glycosylation of individual glycoproteins. 5FU, AraC, MTX and 6MP all influenced both pyrimidine- and purine-mediated sugar incorporation. This excludes, therefore, direct effects of the antimetabolites on their analogue nucleotide-sugars. The antimetabolite-induced changes in glycosylation did not directly correlate with the observed cell-cycle effects of the antimetabolites.

摘要

本研究证实,如我们之前的综述(《欧洲癌症杂志》1990年,第26卷,516 - 523页)所指出的,抗代谢物确实具有改变细胞糖基化的能力。在非致死条件下,将小鼠白血病L1210细胞暴露于各种抗代谢物中。抗代谢物5-氟尿嘧啶(5FU)、阿糖胞苷(AraC)、甲氨蝶呤(MTX)和6-巯基嘌呤(6MP),但不包括6-硫鸟嘌呤,诱导了放射性标记单糖代谢掺入的显著变化。每种抗代谢物都表现出不同的效果。相对于对照值,在从单糖葡糖胺、岩藻糖、甘露糖和半乳糖掺入的放射性方面发现了显著差异。聚丙烯酰胺凝胶电泳表明,个别糖蛋白的糖基化发生了变化。5FU、AraC、MTX和6MP均影响嘧啶和嘌呤介导的糖掺入。因此,这排除了抗代谢物对其类似物核苷酸糖的直接影响。抗代谢物诱导的糖基化变化与所观察到的抗代谢物对细胞周期的影响没有直接关联。

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