Parasite mitogen-activated protein kinases as drug discovery targets to treat human protozoan pathogens.

Journal of signal transduction Pub Date : 2011-01-01 Epub Date: 2011-02-27 DOI:10.1155/2011/971968
Michael J Brumlik, Srilakshmi Pandeswara, Sara M Ludwig, Kruthi Murthy, Tyler J Curiel
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引用次数: 35

Abstract

Protozoan pathogens are a highly diverse group of unicellular organisms, several of which are significant human pathogens. One group of protozoan pathogens includes obligate intracellular parasites such as agents of malaria, leishmaniasis, babesiosis, and toxoplasmosis. The other group includes extracellular pathogens such as agents of giardiasis and amebiasis. An unfortunate unifying theme for most human protozoan pathogens is that highly effective treatments for them are generally lacking. We will review targeting protozoan mitogen-activated protein kinases (MAPKs) as a novel drug discovery approach towards developing better therapies, focusing on Plasmodia, Leishmania, and Toxoplasma, about which the most is known.

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寄生虫丝裂原活化蛋白激酶作为治疗人类原生动物病原体的药物发现靶点。
原生动物病原体是一组高度多样化的单细胞生物,其中一些是重要的人类病原体。一类原生动物病原体包括专性细胞内寄生虫,如疟疾、利什曼病、巴贝斯虫病和弓形虫病的病原体。另一类包括细胞外病原体,如贾第虫病和阿米巴病的病原体。不幸的是,对于大多数人类原生动物病原体来说,一个统一的主题是普遍缺乏针对它们的高效治疗方法。我们将回顾靶向原生动物有丝分裂原活化蛋白激酶(MAPKs)作为一种新的药物发现方法,以开发更好的治疗方法,重点是疟原虫,利什曼原虫和弓形虫,其中已知的最多。
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