Drug-Induced Regulation of Target Expression

被引:122
作者
Iskar, Murat [1 ]
Campillos, Monica [1 ]
Kuhn, Michael [1 ]
Jensen, Lars Juhl [1 ,2 ]
van Noort, Vera [1 ]
Bork, Peer [1 ,3 ]
机构
[1] European Mol Biol Lab, Struct & Computat Biol Unit, Heidelberg, Germany
[2] Univ Copenhagen, Novo Nordisk Fdn, Ctr Prot Res, Fac Hlth Sci, Copenhagen, Denmark
[3] Max Delbruck Ctr Mol Med, Berlin, Germany
关键词
RECEPTOR MESSENGER-RNA; ADRENERGIC-RECEPTORS; AGONIST REGULATION; SMALL MOLECULES; PROFILES; ROBUSTNESS; PREDICTION; PROTEINS; DISEASE; GENOME;
D O I
10.1371/journal.pcbi.1000925
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
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.
引用
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页数:8
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