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对选定的抗肿瘤治疗药物及多药耐药发生原因的综述。

A review of selected anti-tumour therapeutic agents and reasons for multidrug resistance occurrence.

作者信息

Sawicka M, Kalinowska M, Skierski J, Lewandowski W

机构信息

Department of Chemistry, Biatystok Technical University, Zamenhofa 29, 15-435 Biatystok, Poland.

出版信息

J Pharm Pharmacol. 2004 Sep;56(9):1067-81. doi: 10.1211/0022357044265.

Abstract

It is assumed that proteins from the ABC family (i.e., glycoprotein P (Pgp)) and a multidrug resistance associated protein (MRP) play a main role in the occurrence of multidrug resistance (MDR) in tumour cells. Other factors that influence the rise of MDR are mechanisms connected with change in the effectiveness of the glutathione cycle and with decrease in expression of topoisomerases I and II. The aim of this review is to characterize drugs applied in anti-tumour therapy and to describe the present state of knowledge concerning the mechanisms of MDR occurrence, as well as the pharmacological agents applied in reducing this phenomenon.

摘要

据推测,ABC家族的蛋白质(即糖蛋白P(Pgp))和多药耐药相关蛋白(MRP)在肿瘤细胞多药耐药(MDR)的发生中起主要作用。影响MDR产生的其他因素是与谷胱甘肽循环有效性变化以及拓扑异构酶I和II表达降低相关的机制。本综述的目的是对用于抗肿瘤治疗的药物进行表征,并描述有关MDR发生机制以及用于减少这种现象的药理剂的当前知识状态。

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