Literature DB >> 15463447

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

A F Cowman1.   

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.

Entities:  

Year:  1991        PMID: 15463447     DOI: 10.1016/0169-4758(91)90197-v

Source DB:  PubMed          Journal:  Parasitol Today        ISSN: 0169-4758


  8 in total

1.  Bisbenzylisoquinolines as modulators of chloroquine resistance in Plasmodium falciparum and multidrug resistance in tumor cells.

Authors:  F Frappier; A Jossang; J Soudon; F Calvo; P Rasoanaivo; S Ratsimamanga-Urverg; J Saez; J Schrevel; P Grellier
Journal:  Antimicrob Agents Chemother       Date:  1996-06       Impact factor: 5.191

2.  Selection for mefloquine resistance in Plasmodium falciparum is linked to amplification of the pfmdr1 gene and cross-resistance to halofantrine and quinine.

Authors:  A F Cowman; D Galatis; J K Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-01       Impact factor: 11.205

3.  Evidence for a central role for PfCRT in conferring Plasmodium falciparum resistance to diverse antimalarial agents.

Authors:  David J Johnson; David A Fidock; Mathirut Mungthin; Viswanathan Lakshmanan; Amar Bir Singh Sidhu; Patrick G Bray; Stephen A Ward
Journal:  Mol Cell       Date:  2004-09-24       Impact factor: 17.970

4.  Enhancement of drug susceptibility in Plasmodium falciparum in vitro and Plasmodium berghei in vivo by mixed-function oxidase inhibitors.

Authors:  A M Ndifor; R E Howells; P G Bray; J L Ngu; S A Ward
Journal:  Antimicrob Agents Chemother       Date:  1993-06       Impact factor: 5.191

5.  Chloroquine encapsulated in malaria-infected erythrocyte-specific antibody-bearing liposomes effectively controls chloroquine-resistant Plasmodium berghei infections in mice.

Authors:  M Owais; G C Varshney; A Choudhury; S Chandra; C M Gupta
Journal:  Antimicrob Agents Chemother       Date:  1995-01       Impact factor: 5.191

6.  Mefloquine exposure induces cell cycle delay and reveals stage-specific expression of the pfmdr1 gene.

Authors:  Elaine B Bohórquez; Jonathan J Juliano; Hyung-Suk Kim; Steven R Meshnick
Journal:  Antimicrob Agents Chemother       Date:  2012-12-03       Impact factor: 5.191

7.  Drug-regulated expression of Plasmodium falciparum P-glycoprotein homologue 1: a putative role for nuclear receptors.

Authors:  David J Johnson; Andrew Owen; Nick Plant; Patrick G Bray; Stephen A Ward
Journal:  Antimicrob Agents Chemother       Date:  2008-01-14       Impact factor: 5.191

Review 8.  A systematic review and meta-analysis of evidence for correlation between molecular markers of parasite resistance and treatment outcome in falciparum malaria.

Authors:  Stéphane Picot; Piero Olliaro; Frédérique de Monbrison; Anne-Lise Bienvenu; Ric N Price; Pascal Ringwald
Journal:  Malar J       Date:  2009-05-04       Impact factor: 2.979

  8 in total

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