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恶性疟原虫的P-糖蛋白同源物:它们与氯喹耐药性有关吗?

The P-glycoprotein homologues of Plasmodium falciparum: Are they involved in chloroquine resistance?

作者信息

Cowman A F

机构信息

The Walter and Eliza Hall Institute of Medical Research, Post Office, Royal Melbourne Hospital, Victoria 3050, Australia.

出版信息

Parasitol Today. 1991 Apr;7(4):70-6. doi: 10.1016/0169-4758(91)90197-v.

Abstract

Chloroquine has been the mainstay of antimalarial chemotherapy but the rapid spread of resistance to this important drug has now compromised its efficacy. The mechanism of chloroquine resistance has not been known but recent evidence from Plasmodium falciparum, the causative agent of the most severe form of human malaria, suggested similarities to the multidrug resistance phenotype (MDR) of mammalian tumour cells which is mediated by a protein molecule termed P-glycoprotein. Two mdr genes (pfmdr1 and pfmdr2) encoding P-glycoprotein homologues have been identified in P. falciparum and one of these (pfmdr1) has several alleles that have been linked to the chloroquine resistance phenotype. In contrast analysis of a genetic cross between chloroquine-resistant and -sensitive P. falciparum has suggested that the genes encoding the known P-glycoprotein homologues are not linked. This review outlines the similarities of the chloroquine resistance phenotype with the MDR phenotype of mammalian tumour cells and explores the possible role of the pfmdr genes.

摘要

氯喹一直是抗疟化疗的主要药物,但对这种重要药物的耐药性迅速传播,现已损害了其疗效。氯喹耐药机制尚不清楚,但来自人类最严重疟疾致病原恶性疟原虫的最新证据表明,它与哺乳动物肿瘤细胞的多药耐药表型(MDR)有相似之处,后者由一种名为P-糖蛋白的蛋白质分子介导。在恶性疟原虫中已鉴定出两个编码P-糖蛋白同源物的mdr基因(pfmdr1和pfmdr2),其中一个(pfmdr1)有几个与氯喹耐药表型相关的等位基因。相比之下,对氯喹耐药和敏感的恶性疟原虫之间遗传杂交的分析表明,编码已知P-糖蛋白同源物的基因没有联系。本综述概述了氯喹耐药表型与哺乳动物肿瘤细胞MDR表型的相似之处,并探讨了pfmdr基因的可能作用。

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