Cytotoxicity and in-vivo tolerance of FdUMP[10]: a novel pro-drug of the TS inhibitory nucleotide FdUMP.

W H Gmeiner, A Skradis, R T Pon, J Liu
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引用次数: 12

Abstract

The cytotoxicity of the 10mer ODN FdUMP[10] towards human colorectal tumor cells was evaluated using a clonogenic assay. FdUMP[10] was more than 100-fold more active than 5-FU at inhibiting colony formation of H630 cells. FdUMP[10] was also evaluated for cytotoxicity in the NCI 60 cell line screen, and showed markedly improved activity relative to 5-FU against numerous tumor cell lines. The in-vivo tolerance of FdUMP[10] is more than three-fold greater per mole fluorinated pyrimidine, than 5-FU.

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FdUMP的细胞毒性和体内耐受性[10]:一种新的TS抑制核苷酸FdUMP前药。
10mer ODN FdUMP[10]对人类结直肠肿瘤细胞的细胞毒性通过克隆生成实验进行了评估。FdUMP[10]抑制H630细胞集落形成的活性是5-FU的100倍以上。FdUMP[10]也在NCI 60细胞系筛选中进行了细胞毒性评估,与5-FU相比,FdUMP对许多肿瘤细胞系的活性明显提高。每摩尔氟化嘧啶对FdUMP的体内耐受性[10]比5-FU高3倍以上。
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