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星形孢菌素可降低P-糖蛋白表达并调节多药耐药性。

Staurosporine reduces P-glycoprotein expression and modulates multidrug resistance.

作者信息

Sampson K E, Wolf C L, Abraham I

机构信息

Cell Biology Department, Upjohn Company, Kalamazoo, Michigan 49001.

出版信息

Cancer Lett. 1993 Jan 15;68(1):7-14. doi: 10.1016/0304-3835(93)90213-s.

Abstract

We have investigated the effect of staurosporine and other kinase inhibitors on the mRNA and protein levels of the P-glycoprotein (P-gp) in multidrug resistant (MDR) cells. Treatment of human MDR KB-V1 cells with staurosporine for 24 h caused up to a 50% decrease in the amount of P-gp mRNA and protein present. Co-treatment of KB-V1 cells with verapamil, a known reversal agent, plus staurosporine, H-9, or K252a resulted in an enhanced sensitization of cells to vinblastine than with verapamil alone. These findings support a role for protein kinases in the control of multidrug resistance through effects on P-gp levels.

摘要

我们研究了星形孢菌素和其他激酶抑制剂对多药耐药(MDR)细胞中P-糖蛋白(P-gp)的mRNA和蛋白水平的影响。用星形孢菌素处理人MDR KB-V1细胞24小时,导致P-gp mRNA和蛋白的含量下降高达50%。将已知的逆转剂维拉帕米与星形孢菌素、H-9或K252a共同处理KB-V1细胞,与单独使用维拉帕米相比,细胞对长春碱的敏感性增强。这些发现支持蛋白激酶通过影响P-gp水平在多药耐药控制中发挥作用。

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