Hsp90 Inhibitors in Parasitic Nematodes: Prospects and Challenges

被引:5
|
作者
Devaney, Eileen [1 ]
Gillan, Victoria [1 ]
机构
[1] Univ Glasgow, Inst Biodivers Comparat Med & Anim Hlth, Garscube Estate,Bearsden Rd, Glasgow G61 1QH, Lanark, Scotland
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Parasitic nematode; Brugia pahangi; Caenorhabditis elegans; Drug resistance; Hsp90; inhibitors; LYMPHATIC FILARIASIS; DRUG-RESISTANCE; BRUGIA-PAHANGI; HEAT-SHOCK; CAENORHABDITIS-ELEGANS; HELMINTH INFECTIONS; DISCOVERY; EVOLUTION; TARGET; MODEL;
D O I
10.2174/1568026616666160413140502
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Hsp90 inhibitors are well characterized in relation to their effects in a variety of tumors, with several inhibitors in various phases of clinical development. In recent years, the same inhibitor classes have been tested for efficacy in other systems, such as Alzheimer's disease and a variety of infectious disease models, including fungal and parasitic targets. In this article we discuss the re-purposing of Hsp90 inhibitors for parasitic disease with a focus on parasitic nematode infections. We summarize the data that indicate that Hsp90 is functionally diverse in different nematode species and we discuss the challenges and prospects for developing these inhibitors as next generation chemotherapeutic tools.
引用
收藏
页码:2805 / 2811
页数:7
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