La Trobe University, Genetics Department, Bundoora, Vic 3085, Australia +61 3 9479 5067 ; +61 3 9479 5067 ;
Expert Opin Drug Discov. 2007 Oct;2(s1):S91-8. doi: 10.1517/17460441.2.S1.S91.
Anthelmintics presently used in humans were discovered using empirical biological screening processes targeting helminths of veterinary importance. The modern approach to drug discovery is based on genetic, bioinformatic and genomic identification of protein targets followed by specific validation assays and high-throughput screening using chemical libraries. Existing broad-spectrum anthelmintics bind just three classes of molecular targets; more classes of targets are urgently needed. In the absence of robust functional genomics technologies for helminth parasites, the technology of RNA interference in parasites and in the model Caenorhabditis elegans is the best available for discovery and validation of new targets. This article outlines and critically discusses an idealised drug discovery pipeline for anthelmintic discovery in nematodes.
目前用于人类的驱虫药是通过针对具有兽医重要性的寄生虫的经验性生物筛选过程发现的。现代药物发现方法基于遗传、生物信息学和基因组鉴定蛋白质靶标,然后使用化学文库进行特定的验证测定和高通量筛选。现有的广谱驱虫药仅结合三类分子靶标;迫切需要更多类别的靶标。在缺乏针对寄生虫的稳健功能基因组学技术的情况下,寄生虫和模式生物秀丽隐杆线虫中的 RNA 干扰技术是发现和验证新靶标的最佳可用技术。本文概述并批判性地讨论了用于线虫驱虫药发现的理想药物发现管道。