MULTIPLE-DRUG RESISTANCE IN THE PATHOGENIC PROTOZOA

被引:27
作者
UPCROFT, P
机构
[1] Queensland Institute of Medical Research, The Bancroft Centre, Brisbane, QLD 4029
关键词
ATP-BINDING CASSETTE TRANSPORTER; DRUG EFFLUX MECHANISM; MULTIPLE DRUG RESISTANCE (MDR); MDR GENE; PROTOZOAN; TRANSPORTER; DRUG RESISTANCE;
D O I
10.1016/0001-706X(94)90063-9
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Evidence for the phenomenon of multiple drug resistance (MDR) in the well studied pathogenic protozoa has been examined. This has been placed in the more familiar context of the MDR efflux transporters and the cloned mdr genes of mammalian cells. Homologues of the mdr gene family in protozoa and their possible role in drug efflux have been compared with their mammalian counterparts. Possible mechanisms and models for drug efflux have been considered. The unusual and extensive range of substrates transported by the ATP-binding cassette (ABC) family of transporters which includes the MDRs has been raised. The impact of kinetics, structure and bioenergetics of the MDR family members on mechanisms of transport has been accentuated to argue that MDR efflux considered in isolation appears bizarre but may be better understood in a broader context.
引用
收藏
页码:195 / 212
页数:18
相关论文
共 133 条
[1]   THE AMI LOCUS OF THE GRAM-POSITIVE BACTERIUM STREPTOCOCCUS-PNEUMONIAE IS SIMILAR TO BINDING PROTEIN-DEPENDENT TRANSPORT OPERONS OF GRAM-NEGATIVE BACTERIA [J].
ALLOING, G ;
TROMBE, MC ;
CLAVERYS, JP .
MOLECULAR MICROBIOLOGY, 1990, 4 (04) :633-644
[2]   PARTIAL-PURIFICATION AND RECONSTITUTION OF THE HUMAN MULTIDRUG-RESISTANCE PUMP - CHARACTERIZATION OF THE DRUG-STIMULATABLE ATP HYDROLYSIS [J].
AMBUDKAR, SV ;
LELONG, IH ;
ZHANG, JP ;
CARDARELLI, CO ;
GOTTESMAN, MM ;
PASTAN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (18) :8472-8476
[3]   THE BASIS OF MULTIDRUG RESISTANCE IN MAMMALIAN-CELLS - HOMOLOGY WITH BACTERIAL TRANSPORT [J].
AMES, GF .
CELL, 1986, 47 (03) :323-324
[4]  
AMES GF, 1989, J BIOL CHEM, V264, P3998
[5]   ATP-DEPENDENT BACTERIAL TRANSPORTERS AND CYSTIC-FIBROSIS - ANALOGY BETWEEN CHANNELS AND TRANSPORTERS [J].
AMES, GF ;
LECAR, H .
FASEB JOURNAL, 1992, 6 (09) :2660-2666
[6]   MULTIDRUG RESISTANCE GENES, P-GLYCOPROTEIN AND THE LIVER [J].
ARIAS, IM .
HEPATOLOGY, 1990, 12 (01) :159-165
[7]   ENTAMOEBA-HISTOLYTICA - PHYSIOLOGY OF MULTIDRUG RESISTANCE [J].
AYALA, P ;
SAMUELSON, J ;
WIRTH, D ;
OROZCO, E .
EXPERIMENTAL PARASITOLOGY, 1990, 71 (02) :169-175
[8]   DISCRETE MUTATIONS INTRODUCED IN THE PREDICTED NUCLEOTIDE-BINDING SITES OF THE MDR1 GENE ABOLISH ITS ABILITY TO CONFER MULTIDRUG RESISTANCE [J].
AZZARIA, M ;
SCHURR, E ;
GROS, P .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (12) :5289-5297
[9]   MULTIDRUG RESISTANCE AND CYSTIC-FIBROSIS GENES - COMPLEMENTARITY OF FUNCTION [J].
BEAR, C ;
LING, V .
TRENDS IN GENETICS, 1993, 9 (03) :67-68
[10]   PURIFICATION AND FUNCTIONAL RECONSTITUTION OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) [J].
BEAR, CE ;
LI, CH ;
KARTNER, N ;
BRIDGES, RJ ;
JENSEN, TJ ;
RAMJEESINGH, M ;
RIORDAN, JR .
CELL, 1992, 68 (04) :809-818