Suppr超能文献

在人鳞状细胞癌细胞系中,亚叶酸和脱氧核苷增强氟嘧啶对细胞生长的抑制作用。

Enhancement of fluoropyrimidine inhibition of cell growth by leucovorin and deoxynucleosides in a human squamous cell carcinoma cell line.

作者信息

Chang Y M, Bertino J R

机构信息

Program Developmental Therapy, Memorial Sloan-Kettering Cancer Center, New York, New York.

出版信息

Cancer Invest. 1989;7(6):557-63. doi: 10.3109/07357908909017530.

Abstract

The growth inhibitory effects of the fluoropyrimidines 5-fluorouracil (5-FU) and 5-fluoro-2'-deoxyuridine (FdUrd) against a human squamous cell carcinoma cell line (SQ-1) were studied in the absence and presence of deoxynucleosides and/or N5-formyl-tetrahydrofolate (leucovorin). Inhibition of cell growth by the fluoropyrimidines was less when undialyzed rather than dialyzed fetal bovine serum was used. Leucovorin, in concentrations of 10(-6) to 10(-4) M potentiated the growth inhibition of FU and FdUrd; deoxyguanosine and deoxyinosine in concentrations of 10(-5) M also enhanced the growth inhibition produced by these fluoropyrimidines. In the presence of leucovorin addition, deoxyguanosine (10(-5) M) caused a further synergistic inhibition of cell growth produced by FdUrd but not FU. In contrast, addition of deoxyinosine at 10(-5) M resulted in further potentiation of FU but not FdUrd inhibition of cell growth in the presence of leucovorin. The synergy obtained with these combinations encourage the exploration of modulation of fluoropyrimidine by leucovorin and deoxynucleosides in vivo.

摘要

在有无脱氧核苷和/或N5-甲酰四氢叶酸(亚叶酸)的情况下,研究了氟嘧啶5-氟尿嘧啶(5-FU)和5-氟-2'-脱氧尿苷(FdUrd)对人鳞状细胞癌细胞系(SQ-1)的生长抑制作用。当使用未透析而非透析的胎牛血清时,氟嘧啶对细胞生长的抑制作用较小。浓度为10(-6)至10(-4)M的亚叶酸增强了FU和FdUrd的生长抑制作用;浓度为10(-5)M的脱氧鸟苷和脱氧肌苷也增强了这些氟嘧啶产生的生长抑制作用。在添加亚叶酸的情况下,脱氧鸟苷(10(-5)M)对FdUrd而非FU产生的细胞生长有进一步的协同抑制作用。相比之下,在添加亚叶酸的情况下,加入10(-5)M的脱氧肌苷会使FU对细胞生长的抑制作用进一步增强,但对FdUrd没有影响。这些组合产生的协同作用促使人们探索在体内通过亚叶酸和脱氧核苷对氟嘧啶进行调节。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验