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果蝇中的药物筛选;为何、何时以及何时不进行?

Drug screening in Drosophila; why, when, and when not?

作者信息

Su Tin Tin

机构信息

Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado.

Molecular, Cellular and Developmental Biology, University of Colorado Comprehensive Cancer Center, Aurora, Colorado.

出版信息

Wiley Interdiscip Rev Dev Biol. 2019 Nov;8(6):e346. doi: 10.1002/wdev.346. Epub 2019 May 5.

Abstract

The best global seller among oncology drugs in 2018 is lenalidomide, an analog of thalidomide. It took 53 years and a circuitous route from the discovery of thalidomide to approval of an analog for use in treatment of cancer. We understand now a lot more about the genetic and molecular basis of diseases than we did in 1953 when thalidomide was discovered. We have also no shortage of chemical libraries with hundreds of thousands of compounds, both synthetic and natural. What we need are better ways to search among these rich resources for compounds with the potential to do what we want them to do. This review summarizes examples from the literature that make Drosophila melanogaster a good model to screen for drugs, and discusses knowledge gaps and technical challenges that make Drosophila models not as widely used as they could or should be. This article is categorized under: Technologies > Analysis of Cell, Tissue, and Animal Phenotypes.

摘要

2018年肿瘤药物中全球最畅销的是来那度胺,它是沙利度胺的类似物。从沙利度胺的发现到其类似物获批用于癌症治疗,历经了53年且道路曲折。如今,我们对疾病的遗传和分子基础的了解比1953年发现沙利度胺时多得多。我们也不乏拥有成千上万种合成和天然化合物的化学文库。我们所需要的是更好的方法,以便在这些丰富的资源中筛选出有潜力实现我们预期功能的化合物。这篇综述总结了文献中的实例,这些实例表明黑腹果蝇是筛选药物的良好模型,并讨论了使果蝇模型未能像其可能或应该的那样被广泛应用的知识空白和技术挑战。本文分类如下:技术>细胞、组织和动物表型分析。

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