Roed H, Christensen I B, Vindeløv L L, Spang-Thomsen M, Hansen H H
Department of Oncology II, Finsen Institute, Copenhagen, Denmark.
Eur J Cancer Clin Oncol. 1987 Feb;23(2):177-86. doi: 10.1016/0277-5379(87)90012-5.
Sensitivity of five human small cell lung cancer cell lines to doxorubicin was assessed by a double layer agar technique using two different bottom-layers. Neither of the bottom-layers provided proportionality between numbers of cells plated and numbers of colonies, but they were correlated by a logarithmic function. Even after correction for lack of proportionality the two assay systems provided significantly different dose-response curves. The stability of the chemosensitivity was tested after 25-30 weeks continuous in vitro culture or prolonged storage in liquid nitrogen. One cell line underwent significant changes after continuous in vitro culture whereas the cell lines tested after prolonged storage in liquid nitrogen showed only minor changes. It is concluded that instead of considering the concentration necessary to achieve a certain degree of cell kill (e.g. ID50) in one experiment on one cell line, dose-response curves obtained on several cell lines in different assay systems should be used in the evaluation of new drugs.
采用双层琼脂技术,使用两种不同的底层琼脂,评估了五种人小细胞肺癌细胞系对阿霉素的敏感性。两种底层琼脂均未使接种的细胞数量与集落数量呈比例关系,但二者通过对数函数相关联。即使校正了不成比例的情况,两种检测系统的剂量反应曲线仍有显著差异。在体外连续培养25 - 30周或在液氮中长时间保存后,检测了化学敏感性的稳定性。一种细胞系在体外连续培养后发生了显著变化,而在液氮中长时间保存后检测的细胞系仅显示出微小变化。得出的结论是,在评估新药时,不应仅考虑在一个细胞系的一次实验中达到一定程度细胞杀伤所需的浓度(如ID50),而应使用在不同检测系统中多个细胞系获得的剂量反应曲线。