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新型亚硝基脲药物福莫司汀与5-氟尿嘧啶加亚叶酸联合使用的序列依赖性细胞毒性作用

Sequence-dependent cytotoxic effects of the combination of a new nitrosourea, fotemustine, with 5-fluorouracil plus folinic acid.

作者信息

Fischel J L, Formento P, Berlion M, Berille J, Gioanni J, Bizzari J P, Milano G

机构信息

Centre Antoine-Lacassagne, Nice, France.

出版信息

Cancer Chemother Pharmacol. 1991;28(6):448-54. doi: 10.1007/BF00685821.

DOI:10.1007/BF00685821
PMID:1657424
Abstract

The present study was designed to analyse the cytotoxic effects of the combination of fotemustine with 5-fluorouracil (5-FU) plus folinic acid (FA). Two human tumor cell lines were used; one line was derived from colon cancer (WIDR) and the other, from a non-small-cell lung cancer (CAL 12). Cytotoxic effects were assessed using the MTT (tetrazolium bromide) semi-automated test in 96-well incubation plates. The effects of various drug combinations were evaluated by the isobologram method. The drug combinations tested included fotemustine concentrations of 20, 30, 40, 50 and 70 micrograms/ml, 5-FU concentrations of 5, 15 and 30 micrograms/ml, and a constant FA concentration of 10(-5) M. A total of 180 different experimental conditions were tested. When cells were exposed to fotemustine prior to treatment with 5-FU, the final cytotoxic effects on both cell lines were additive or synergistic in the majority of cases (P less than 0.001). The 5-FU concentration was a determinant factor that modified the effects of the drug combination from antagonism (at low 5-FU concentrations) to synergism (high 5-FU concentrations; P less than 0.001). The addition of FA (10(-5) M) resulted in a significant shift towards synergistic associations in both cell lines. Administration of 5-FU prior to treatment with fotemustine caused marked antagonism, which 10(-5) M FA could not significantly shift towards simple additivity.

摘要

本研究旨在分析福莫司汀与5-氟尿嘧啶(5-FU)加亚叶酸(FA)联合使用的细胞毒性作用。使用了两种人类肿瘤细胞系;一种源自结肠癌(WIDR),另一种源自非小细胞肺癌(CAL 12)。使用MTT(溴化四氮唑)半自动试验在96孔培养板中评估细胞毒性作用。通过等效线图法评估各种药物组合的效果。测试的药物组合包括浓度为20、30、40、50和70微克/毫升的福莫司汀,浓度为5、15和30微克/毫升的5-FU,以及恒定浓度为10^(-5) M的FA。总共测试了180种不同的实验条件。当细胞在用5-FU治疗之前先接触福莫司汀时,在大多数情况下,对两种细胞系的最终细胞毒性作用是相加或协同的(P<0.001)。5-FU浓度是一个决定因素,它将药物组合的作用从拮抗(在低5-FU浓度下)改变为协同(高5-FU浓度;P<0.001)。添加FA(10^(-5) M)导致两种细胞系的协同联合显著增加。在用福莫司汀治疗之前给予5-FU会引起明显的拮抗作用,10^(-5) M的FA无法将其显著转变为简单相加作用。

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