Mircheva J, Tsuruo T
Dept. of Experimental Therapy of Tumors, Medical Academy, Sofia, Bulgaria.
Tumori. 1990 Oct 31;76(5):450-4. doi: 10.1177/030089169007600506.
The effect of the calcium antagonists cepharanthine and verapamil on adriamycin-induced cytotoxicity against sensitive (K 562 and Ov 2780) and resistant (K 562/ADM and AD 10) sublines of human tumor cells was evaluated. Nontoxic concentrations of cepharanthine moderately enhanced adriamycin cytotoxicity against sensitive sublines (2.1-2.5 fold). A significant enhancement (13-26 fold) of drug cytotoxicity was observed when resistant cells were treated with a combination of cepharanthine and adriamycin. The calcium influx blocker verapamil (used for comparison) also enhanced adriamycin cytotoxicity, although to a lesser extent. The fact that enhancement was 6-10 fold greater in resistant then in sensitive cells, as well as the loss of biphasic properties of adriamycin on dose-response curves after combined treatment, indicate that cepharanthine may play a role in overcoming drug resistance in some tumor cells.
评估了钙拮抗剂千金藤素和维拉帕米对阿霉素诱导的针对人肿瘤细胞敏感亚系(K 562和Ov 2780)及耐药亚系(K 562/ADM和AD 10)的细胞毒性作用。无毒浓度的千金藤素适度增强了阿霉素对敏感亚系的细胞毒性(2.1 - 2.5倍)。当耐药细胞用千金藤素和阿霉素联合处理时,观察到药物细胞毒性显著增强(13 - 26倍)。作为对照的钙内流阻滞剂维拉帕米也增强了阿霉素的细胞毒性,尽管程度较小。耐药细胞中增强作用比敏感细胞大6 - 10倍,以及联合处理后阿霉素剂量反应曲线双相特性的丧失,表明千金藤素可能在克服某些肿瘤细胞的耐药性中发挥作用。