首页> 外文期刊>Bioscience Reports >Verapamil and cyclosporin a sensitize human kidney tumor cells to vincristine in absence of membrane P-glycoprotein and without apparent changes in the cytoplasmic free Ca2+ concentration
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Verapamil and cyclosporin a sensitize human kidney tumor cells to vincristine in absence of membrane P-glycoprotein and without apparent changes in the cytoplasmic free Ca2+ concentration

机译:维拉帕米和环孢菌素a在缺乏膜P-糖蛋白且细胞质游离Ca2 +浓度无明显变化的情况下使人肾肿瘤细胞对长春新碱敏感

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Vincristine (Vcr) dose dependently inhibited growth of the kidney adenocarcinoma cell line ACHN during 4 days of culture. Verapamil (Ver) at 10 μM and cyclosporin A (CsA) at 1 μg/ml had no effect on cell growth but significantly potentiated the action of Vcr, despite the absence of the multidrug resistance associated membrane P-glycoprotein (P-gp). Neither Ver nor CsA had any acute or long term effects on cytoplasmic free Ca2+ concentration (Ca2+i), except for a small Ver induced increase after 36 h of incubation. The results indicate that Ver and CsA may have a sensitizing effect on chemotherapeutic drug sensitivity also in absence of P-gp. However, these effects are probably not mediated by changes in Ca2+i.
机译:长春新碱(Vcr)剂量依赖性地在培养4天期间抑制肾腺癌细胞系ACHN的生长。尽管没有多药耐药性相关的膜P-糖蛋白(P-gp),但10μM的维拉帕米(Ver)和1μg/ ml的环孢菌素A(CsA)对细胞生长没有影响,但显着增强了Vcr的作用。 Ver和CsA均未对细胞质中的游离Ca2 +浓度(Ca2 + i)产生任何急性或长期影响,但在孵育36小时后有少量Ver诱导增加。结果表明,在不存在P-gp的情况下,Ver和CsA对化疗药物敏感性也可能具有敏化作用。但是,这些作用可能不是由Ca2 + i的变化介导的。

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