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使用DNA微阵列进行药物靶点验证及次要药物靶点效应的鉴定。

Drug target validation and identification of secondary drug target effects using DNA microarrays.

作者信息

Marton M J, DeRisi J L, Bennett H A, Iyer V R, Meyer M R, Roberts C J, Stoughton R, Burchard J, Slade D, Dai H, Bassett D E, Hartwell L H, Brown P O, Friend S H

机构信息

Rosetta Inpharmatics, Kirkland, Washington 98034, USA.

出版信息

Nat Med. 1998 Nov;4(11):1293-301. doi: 10.1038/3282.

Abstract

We describe here a method for drug target validation and identification of secondary drug target effects based on genome-wide gene expression patterns. The method is demonstrated by several experiments, including treatment of yeast mutant strains defective in calcineurin, immunophilins or other genes with the immunosuppressants cyclosporin A or FK506. Presence or absence of the characteristic drug 'signature' pattern of altered gene expression in drug-treated cells with a mutation in the gene encoding a putative target established whether that target was required to generate the drug signature. Drug dependent effects were seen in 'targetless' cells, showing that FK506 affects additional pathways independent of calcineurin and the immunophilins. The described method permits the direct confirmation of drug targets and recognition of drug-dependent changes in gene expression that are modulated through pathways distinct from the drug's intended target. Such a method may prove useful in improving the efficiency of drug development programs.

摘要

我们在此描述一种基于全基因组基因表达模式进行药物靶点验证及鉴定药物次要靶点效应的方法。该方法通过多项实验得以证明,包括用免疫抑制剂环孢素A或FK506处理在钙调神经磷酸酶、亲免素或其他基因方面存在缺陷的酵母突变菌株。在编码假定靶点的基因发生突变的药物处理细胞中,是否存在基因表达改变的特征性药物“特征”模式,确定了该靶点是否是产生药物特征所必需的。在“无靶点”细胞中观察到了药物依赖性效应,表明FK506会影响独立于钙调神经磷酸酶和亲免素的其他途径。所描述的方法能够直接确认药物靶点,并识别通过不同于药物预期靶点的途径调节的药物依赖性基因表达变化。这样一种方法可能对提高药物开发项目的效率有用。

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