Hartwell L H, Szankasi P, Roberts C J, Murray A W, Friend S H
Seattle Project, Molecular Pharmacology Department, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Science. 1997 Nov 7;278(5340):1064-8. doi: 10.1126/science.278.5340.1064.
The discovery of anticancer drugs is now driven by the numerous molecular alterations identified in tumor cells over the past decade. To exploit these alterations, it is necessary to understand how they define a molecular context that allows increased sensitivity to particular compounds. Traditional genetic approaches together with the new wealth of genomic information for both human and model organisms open up strategies by which drugs can be profiled for their ability to selectively kill cells in a molecular context that matches those found in tumors. Similarly, it may be possible to identify and validate new targets for drugs that would selectively kill tumor cells with a particular molecular context. This article outlines some of the ways that yeast genetics can be used to streamline anticancer drug discovery.
过去十年间,肿瘤细胞中发现的众多分子改变推动了抗癌药物的研发。为了利用这些改变,有必要了解它们如何界定一种分子环境,从而使细胞对特定化合物更敏感。传统遗传学方法以及人类和模式生物新获得的大量基因组信息,为我们开辟了一些策略,通过这些策略,可以根据药物在与肿瘤中发现的分子环境相匹配的分子环境中选择性杀死细胞的能力对药物进行分析。同样,有可能识别并验证能够在特定分子环境下选择性杀死肿瘤细胞的新药物靶点。本文概述了利用酵母遗传学简化抗癌药物研发的一些方法。