Drake J C, Voeller D M, Allegra C J, Johnston P G
NCI-Navy Medical Oncology Branch, Bethesda, Maryland 20889-5105, USA.
Br J Cancer. 1995 Jun;71(6):1145-50. doi: 10.1038/bjc.1995.224.
We examined the importance of dosing interval between leucovorin (LCV) and 5-fluorouracil (5-FU) on intracellular thymidylate synthase (TS) ternary complex, free TS and total TS protein levels in human MCF-7 breast and NCI H630 colon cancer cell lines. A 2- to 3-fold increase in total TS was noted when either cell line was exposed to 5-FU 10 microM plus LCV (0.01-10 microM) compared with a 1.4- to 1.6-fold increase in total TS due to 5-FU 10 microM alone. The amount of TS ternary complex formed was 2- to 3-fold higher in both cell lines treated with the combination of 5-FU and LCV compared with 5-FU alone. TS complex formation and total TS protein increased with LCV dose (0.1-10 microM). In MCF-7 cells, the maximal increase in total TS protein and TS ternary complex formation was observed when 5-FU was delayed for 4 h after the start of LCV exposure. In NCI H630 cells, maximal total TS protein and ternary complex formation occurred when 5-FU was delayed for 18 h after the start of LCV exposure. The amount of free TS did not change in either cell line whether 5-FU was given concurrently with LCV or delayed for up to 24 h. The accumulation rate of intracellular folates in the form of higher glutamates Glu3-Glu5 was rapid in MCF-7 cells (maximal formation after 4 h), whereas in H630 cells accumulation of higher polyglutamates continued to increase up to 18 h. The time of peak folate polyglutamate (Glu3-Glu5) formation coincided with the time of peak TS complex formation and total TS protein in each cell line. In these human carcinoma cell lines, the LCV dose and interval between 5-FU and LCV play a role in increased TS total protein and TS ternary complex; however, the amount of free TS is independent of the interval between 5-FU and LCV. The time-and dose-dependent increases in TS ternary complex and TS total protein are associated with differences in the accumulation of folate polyglutamates in these cell lines.
我们研究了亚叶酸(LCV)与5-氟尿嘧啶(5-FU)给药间隔对人MCF-7乳腺癌细胞系和NCI H630结肠癌细胞系中细胞内胸苷酸合成酶(TS)三元复合物、游离TS及总TS蛋白水平的重要性。当任一细胞系暴露于10微摩尔5-FU加LCV(0.01 - 10微摩尔)时,总TS增加了2至3倍,而单独使用10微摩尔5-FU时总TS增加了1.4至1.6倍。与单独使用5-FU相比,在同时使用5-FU和LCV处理的两种细胞系中形成的TS三元复合物量高出2至3倍。TS复合物的形成及总TS蛋白随LCV剂量(0.1 - 10微摩尔)增加。在MCF-7细胞中,当在开始暴露LCV后延迟4小时给予5-FU时,观察到总TS蛋白和TS三元复合物形成的最大增加。在NCI H630细胞中,当在开始暴露LCV后延迟18小时给予5-FU时,出现最大总TS蛋白和三元复合物形成。无论5-FU是与LCV同时给予还是延迟长达24小时,任一细胞系中的游离TS量均未改变。在MCF-7细胞中,以较高谷氨酸盐Glu3 - Glu5形式存在的细胞内叶酸积累速率很快(4小时后形成最大量),而在H630细胞中,较高多聚谷氨酸盐的积累持续增加直至18小时。每个细胞系中叶酸多聚谷氨酸(Glu3 - Glu5)形成的峰值时间与TS复合物形成峰值时间及总TS蛋白峰值时间一致。在这些人癌细胞系中,LCV剂量以及5-FU与LCV之间的间隔在增加TS总蛋白和TS三元复合物方面起作用;然而,游离TS的量与5-FU和LCV之间的间隔无关。TS三元复合物和TS总蛋白的时间和剂量依赖性增加与这些细胞系中叶酸多聚谷氨酸积累的差异相关。