Comparative folate metabolism in humans and malaria parasites (part II):: activities as yet untargeted or specific to Plasmodium

被引:41
作者
Nzila, A
Ward, SA
Marsh, K
Sims, PFG
Hyde, JE
机构
[1] Wellcome Trust Res Labs, Kenya Med Res Inst, Nairobi 00100, Kenya
[2] Wellcome Trust Res Labs, Wellcome Trust Collaborat Res Program, Nairobi 00100, Kenya
[3] Univ Liverpool, Dept Pharmacol & Therapeut, Liverpool L69 3BX, Merseyside, England
[4] Univ Liverpool, Liverpool Sch Trop Med, Liverpool L53 QA, Merseyside, England
[5] Ctr Geog Med Res, Kenya Med Res Inst, Kilifi, Kenya
[6] Ctr Geog Med Res, Wellcome Trust Collaborat Res Program, Kilifi, Kenya
[7] John Radcliffe Hosp, Nuffield Dept Med, Oxford OX3 9DU, England
[8] Univ Manchester, Fac Life Sci, Manchester M60 1QD, Lancs, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.pt.2005.05.008
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
The follate pathway represents a powerful target for combating rapidly dividing systems such as cancer cells, bacteria and malaria parasites. Whereas folate metabolism in mammalian cells and bacteria has been studied extensively, it is understood less well in malaria parasites. In two articles, we attempt to reconstitute the malaria folate pathway based on available information from mammalian and microbial systems, in addition to Plasmodium-genome-sequencing projects. In part 1, we focused on folate enzymes that are already used clinically as anticancer drug targets or that are under development in drug-discovery programs. In this article, we discuss mammalian folate enzymes that have not yet been exploited as potential drug targets, and enzymes that function in the de novo folate-synthesis pathway of the parasite - a particularly attractive area of attack because of its absence from the mammalian host.
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页码:334 / 339
页数:6
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