Jonsson E, Fridborg H, Csóka K, Dhar S, Sundström C, Nygren P, Larsson R
Division of Clinical Pharmacology, University Hospital, Uppsala University, Sweden.
Br J Cancer. 1997;76(2):211-9. doi: 10.1038/bjc.1997.364.
The cytotoxic activity and cross-resistance pattern of the novel topoisomerase I inhibitor topotecan (Topo) were investigated in ten cell lines, representing different mechanisms of cytotoxic drug resistance, and in 218 fresh human tumour samples using the fluorometric microculture cytotoxicity assay (FMCA). Resistance to Topo in the cell lines was associated with expression of the multidrug resistance-associated protein (MRP), whereas the cell lines with P-glycoprotein (P-gp), topoisomerase II and glutathione-associated resistance did not show decreased sensitivity to the drug. Topo was more active in haematological than in solid tumour samples, but substantial activity was observed in carcinomas of the ovary and breast, sarcoma and childhood solid tumours. Cross-resistance to standard drugs representing different mechanisms of action was generally low in patient cells. The effect of Topo was better after longer exposure, but this time-dependent effect was largely abolished when adjustment for in vitro exposure was made. Topo showed activity both in proliferative and non-proliferative cell systems. The results indicate that Topo is insensitive to major mechanisms of resistance except for MRP. Proliferation does not seem to be necessary for the effect of Topo, and no superiority for protracted dosing schedules was observed. The results also suggest that, for example, leukaemias, lymphomas, sarcomas and childhood solid tumours may be suitable targets for future phase II trials.
使用荧光微量培养细胞毒性试验(FMCA),在代表细胞毒性药物耐药不同机制的10种细胞系以及218份新鲜人肿瘤样本中,研究了新型拓扑异构酶I抑制剂拓扑替康(Topo)的细胞毒性活性和交叉耐药模式。细胞系中对Topo的耐药与多药耐药相关蛋白(MRP)的表达有关,而具有P-糖蛋白(P-gp)、拓扑异构酶II和谷胱甘肽相关耐药的细胞系对该药物的敏感性并未降低。Topo在血液学样本中的活性高于实体瘤样本,但在卵巢癌、乳腺癌、肉瘤和儿童实体瘤中观察到显著活性。在患者细胞中,对代表不同作用机制的标准药物的交叉耐药通常较低。较长时间暴露后Topo的效果更好,但在对体外暴露进行校正后,这种时间依赖性效应在很大程度上被消除。Topo在增殖性和非增殖性细胞系统中均显示出活性。结果表明,除MRP外,Topo对主要耐药机制不敏感。增殖似乎不是Topo发挥作用所必需的,且未观察到延长给药方案的优越性。结果还表明,例如白血病、淋巴瘤、肉瘤和儿童实体瘤可能是未来II期试验的合适靶点。