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A genome-wide positioning systems network algorithm for in silico drug repurposing

机译:用于全基因组药物重定位的全基因组定位系统网络算法

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摘要

Recent advances in DNA/RNA sequencing have made it possible to identify new targets rapidly and to repurpose approved drugs for treating heterogeneous diseases by the ‘precise’ targeting of individualized disease modules. In this study, we develop a Genome-wide Positioning Systems network (GPSnet) algorithm for drug repurposing by specifically targeting disease modules derived from individual patient’s DNA and RNA sequencing profiles mapped to the human protein-protein interactome network. We investigate whole-exome sequencing and transcriptome profiles from ~5,000 patients across 15 cancer types from The Cancer Genome Atlas. We show that GPSnet-predicted disease modules can predict drug responses and prioritize new indications for 140 approved drugs. Importantly, we experimentally validate that an approved cardiac arrhythmia and heart failure drug, ouabain, shows potential antitumor activities in lung adenocarcinoma by uniquely targeting a HIF1α/LEO1-mediated cell metabolism pathway. In summary, GPSnet offers a network-based, in silico drug repurposing framework for more efficacious therapeutic selections.
机译:DNA / RNA测序的最新进展使得通过“精确”靶向个体化疾病模块,可以快速确定新的靶标并将已批准的药物用于治疗异质性疾病。在这项研究中,我们开发了一种针对基因组定位的全基因组定位系统网络(GPSnet)算法,其方法是专门针对疾病模块,这些疾病模块来自个体患者的DNA和RNA测序图谱,并映射到人类蛋白质-蛋白质相互作用组网络上。我们研究了来自癌症基因组图谱的15种癌症类型中约5,000名患者的全外显子组测序和转录组谱。我们表明,GPSnet预测的疾病模块可以预测药物反应,并对140种已批准药物的新适应症进行优先排序。重要的是,我们通过实验验证了批准的心律不齐和心力衰竭药物ouabain通过独特地靶向HIF1α/ LEO1介导的细胞代谢途径,在肺腺癌中显示出潜在的抗肿瘤活性。总之,GPSnet为更有效的治疗选择提供了基于网络的计算机模拟药物再利用框架。

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