Roed H, Aabo K, Vindeløv L, Spang-Thomsen M, Christensen I B, Hansen H H
Department of Oncology B, Finsen Institute, Copenhagen, Denmark.
Eur J Cancer Clin Oncol. 1989 Aug;25(8):1197-201. doi: 10.1016/0277-5379(89)90415-x.
As the indoloquinone EO-9 has previously shown activity in several tumor model systems it was evaluated against four human small cell lung cancer cell lines by the clonogenic assay. In two cell lines (Nyh and Tol), exponential dose-response curves were achieved with both 1 h and continuous exposure, whereas no cell kill was obtained in the other two cell lines (69 and 592) when tested with 1 h incubation up to 0.25 microgram/ml. When the cells were exposed to drug in vitro, flow cytometric DNA analysis showed perturbations in the cell cycle distribution of the most sensitive cell line (Tol) at a lower EO-9 concentration than in the less sensitive cel line (592). This in vitro predicted difference in EO-9 sensitivity between two of the cell lines (592 and Tol) was confirmed when the cell lines were heterotransplanted to nude mice.
由于吲哚醌EO - 9此前已在多个肿瘤模型系统中显示出活性,因此通过克隆形成试验对其针对四种人小细胞肺癌细胞系进行了评估。在两个细胞系(Nyh和Tol)中,1小时暴露和持续暴露均获得了指数剂量反应曲线,而在另外两个细胞系(69和592)中,当以1小时孵育测试直至0.25微克/毫升时,未观察到细胞杀伤。当细胞在体外暴露于药物时,流式细胞术DNA分析显示,在比敏感性较低的细胞系(592)更低的EO - 9浓度下,最敏感的细胞系(Tol)的细胞周期分布出现紊乱。当将这两个细胞系异种移植到裸鼠体内时,证实了体外预测的这两个细胞系(592和Tol)之间EO - 9敏感性的差异。