Holmberg M, Sandberg C, Nygren P, Larsson R
Department of Infectious Diseases, University Hospital, Uppsala University, Sweden.
Anticancer Drugs. 1994 Oct;5(5):598-600. doi: 10.1097/00001813-199410000-00012.
Using a fluorometric microculture cytotoxicity assay for measuring cell viability and proliferation we examine the cytotoxic effect of lovastatin on a drug sensitive myeloma cell line (RPMI 8226) and a multidrug resistant (MDR) clone (8226/Dox40), that was approximately 100-fold less sensitive to doxorubicin. The RPMI 8226 cells were sensitive to lovastatin with an IC50 of 15.8 micrograms/ml. However, the MDR subline exhibited a collateral sensitivity to lovastatin, with an IC50 of 1.7 microM, thus having a 9.3-fold greater sensitivity to lovastatin than the parental cell line. The combination of doxorubicin and lovastatin did not show any synergistic or antagonistic effects on any of the cell lines. The increased sensitivity to lovastatin of the P-gp 170-expressing MDR cells 8226/Dox40 might be part of a more general phenomenon that merits further investigation.
我们使用荧光微量培养细胞毒性试验来测量细胞活力和增殖,研究洛伐他汀对药物敏感的骨髓瘤细胞系(RPMI 8226)和多药耐药(MDR)克隆(8226/Dox40)的细胞毒性作用,该克隆对阿霉素的敏感性约低100倍。RPMI 8226细胞对洛伐他汀敏感,IC50为15.8微克/毫升。然而,MDR亚系对洛伐他汀表现出旁侧敏感性,IC50为1.7微摩尔,因此对洛伐他汀的敏感性比亲代细胞系高9.3倍。阿霉素和洛伐他汀的联合使用对任何细胞系均未显示出协同或拮抗作用。表达P - gp 170的MDR细胞8226/Dox40对洛伐他汀敏感性增加可能是一个更普遍现象的一部分,值得进一步研究。