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Synergism between 5-fluorouracil and N-methylformamide in HT29 human colon cancer line

机译:5-氟尿嘧啶与N-甲基甲酰胺在HT29人结肠癌细胞系中的协同作用

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In HT29 cells 5-fluorouracil (5FU) cytotoxicity is enhanced by subsequent incubation of cells in medium containing 1% N-methylformamide (NMF). This enhancement does not appear to be related to differences in the repair of 5FU-induced DNA damage. It is proposed that the inhibition of DNA synthesis by NMF (that is reversible and does not result in any detectable toxicity) becomes a lethal event in a cell in which DNA synthesis has already been altered by 5FU exposure. The synergism is sequence dependent (i.e. it does not occur when NMF is given before 5FU) and specific for some cell types as shown by the fact that no synergism was found in L1210 mouse leukaemia cells. In nude mice transplanted s.c. with HT29 cells daily 5FU treatment (for 5 days) followed by daily NMF treatment (for 10 days) caused much greater inhibition of tumour growth than either drug alone or the same combination given in the opposite order (NMF then 5FU). These results, if confirmed on other human colon tumours, could be of clinical interest as a means of increasing the therapeutic efficacy of 5FU in patients with colon cancer.
机译:在HT29细胞中,通过随后在含有1%N-甲基甲酰胺(NMF)的培养基中孵育细胞,可以增强5-氟尿嘧啶(5FU)的细胞毒性。这种增强似乎与5FU诱导的DNA损伤修复的差异无关。有人提出,NMF对DNA合成的抑制作用(可逆且不会导致任何可检测的毒性)在已经通过5FU暴露改变了DNA合成的细胞中成为致命事件。协同作用是序列依赖性的(即在5FU之前给予NMF时不会发生),并且对某些细胞类型具有特异性,如L1210小鼠白血病细胞中未发现协同作用的事实所示。在裸鼠皮下移植每天使用HT29细胞进行5FU治疗(连续5天),然后每天进行NMF治疗(连续10天),与单独使用药物或以相反顺序给药的相同组合(先用NMF再使用5FU)相比,对肿瘤生长的抑制作用要大得多。这些结果,如果在其他人类结肠肿瘤上得到证实,则可能作为增加5FU对结肠癌患者疗效的手段具有临床意义。

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