Lee Y S, Sayeed M M, Wurster R D
Department of Physiology, Loyola University Medical Center, Maywood, IL 60153.
Cancer Lett. 1993 Aug 16;72(1-2):77-81. doi: 10.1016/0304-3835(93)90014-z.
SK&F 96365, a reported receptor-operated Ca2+ channel blocker, inhibited the growth of U-373 MG human astrocytoma and SK-N-MC human neuroblastoma cell lines in a dose-dependent manner. Carbachol and serum which act as growth factors for these cells induced a rapid, transient increase of intracellular Ca2+ concentration without a sustained increase. SK&F 96365 also exerted a significant inhibition of carbachol or serum-induced intracellular Ca2+ mobilization. These results suggest that SK&F 96365 is a potent inhibitor of brain tumor cell growth and that its effect may be mediated by the inhibition of agonist-induced intracellular Ca2+ mobilization.
据报道,SK&F 96365是一种受体操纵的钙离子通道阻滞剂,它以剂量依赖的方式抑制U-373 MG人星形细胞瘤和SK-N-MC人神经母细胞瘤细胞系的生长。作为这些细胞生长因子的卡巴胆碱和血清可诱导细胞内钙离子浓度迅速短暂升高,但无持续升高。SK&F 96365对卡巴胆碱或血清诱导的细胞内钙离子动员也有显著抑制作用。这些结果表明,SK&F 96365是脑肿瘤细胞生长的有效抑制剂,其作用可能是通过抑制激动剂诱导的细胞内钙离子动员来介导的。