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药物诱导的靶标表达调控。

Drug-induced regulation of target expression.

机构信息

Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

PLoS Comput Biol. 2010 Sep 9;6(9):e1000925. doi: 10.1371/journal.pcbi.1000925.

Abstract

Drug perturbations of human cells lead to complex responses upon target binding. One of the known mechanisms is a (positive or negative) feedback loop that adjusts the expression level of the respective target protein. To quantify this mechanism systems-wide in an unbiased way, drug-induced differential expression of drug target mRNA was examined in three cell lines using the Connectivity Map. To overcome various biases in this valuable resource, we have developed a computational normalization and scoring procedure that is applicable to gene expression recording upon heterogeneous drug treatments. In 1290 drug-target relations, corresponding to 466 drugs acting on 167 drug targets studied, 8% of the targets are subject to regulation at the mRNA level. We confirmed systematically that in particular G-protein coupled receptors, when serving as known targets, are regulated upon drug treatment. We further newly identified drug-induced differential regulation of Lanosterol 14-alpha demethylase, Endoplasmin, DNA topoisomerase 2-alpha and Calmodulin 1. The feedback regulation in these and other targets is likely to be relevant for the success or failure of the molecular intervention.

摘要

药物干扰人体细胞会在与靶标结合后产生复杂的反应。其中一种已知的机制是(正或负)反馈回路,它可以调节相应靶标蛋白的表达水平。为了在系统范围内以无偏倚的方式量化这种机制,我们使用连接图谱(Connectivity Map)在三种细胞系中检查了药物靶标 mRNA 的药物诱导差异表达。为了克服该有价值资源中的各种偏差,我们开发了一种计算归一化和评分程序,适用于异质药物处理时的基因表达记录。在研究的 167 个药物靶标中的 466 种作用于 1290 种药物靶标关系中,8%的靶标在 mRNA 水平受到调节。我们系统地证实,特别是作为已知靶标的 G 蛋白偶联受体,在药物治疗时会受到调节。我们进一步新发现了药物诱导的羊毛甾醇 14-α 脱甲基酶、内质网蛋白、DNA 拓扑异构酶 2-α 和钙调蛋白 1 的差异调节。这些和其他靶标中的反馈调节可能与分子干预的成败有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b01/2936514/81f02aa5ab9d/pcbi.1000925.g001.jpg

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