Ho D H, Townsend L, Luna M A, Bodey G P
Anticancer Res. 1986 Jul-Aug;6(4):781-4.
Dihydrouracil dehydrogenase activity, with 5-fluorouracil used as the substrate, was measured in human tissues and leukemic cells. The liver had the highest enzyme activity (mean, 705 nmoles/g tissue/hr) with minimal activity found in the kidneys, spleen, lung, colon, colon tumors, pancreas, breast tissue, breast tumors, bone marrow cells, and peripheral leukemic cells. Wide variations in the enzyme activities were noted in samples collected from different subjects. 5-diazouracil inhibits the enzyme activity with the concentration required for inhibiting 50% (IC50) of the liver enzyme being 3 microM. Other compounds, thymine, thymidine, 6-methoxydiazouracil, and cyclo-5-diazouridine were also tested for their effect on this enzyme. With the exception of cyclo-5-diazouridine, all others produced inhibitory effect. The inhibitory effect of 6-methoxydiazouracil is similar to that of diazouracil. Thymidine and thymine are less active with identical values for IC50 of 80 microM.
以5-氟尿嘧啶为底物,测定了人体组织和白血病细胞中的二氢尿嘧啶脱氢酶活性。肝脏的酶活性最高(平均为705纳摩尔/克组织/小时),而在肾脏、脾脏、肺、结肠、结肠肿瘤、胰腺、乳腺组织、乳腺肿瘤、骨髓细胞和外周白血病细胞中活性最低。在从不同受试者采集的样本中,酶活性存在很大差异。5-重氮尿嘧啶抑制酶活性,抑制肝脏酶50%(IC50)所需的浓度为3微摩尔。还测试了其他化合物胸腺嘧啶、胸腺嘧啶核苷、6-甲氧基重氮尿嘧啶和环5-重氮尿苷对该酶的影响。除环5-重氮尿苷外,其他所有化合物均产生抑制作用。6-甲氧基重氮尿嘧啶的抑制作用与重氮尿嘧啶相似。胸腺嘧啶核苷和胸腺嘧啶的活性较低,IC50值相同,均为80微摩尔。