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

  • Feixiong Cheng
  • , Weiqiang Lu
  • , Chuang Liu
  • , Jiansong Fang
  • , Yuan Hou
  • , Diane E. Handy
  • , Ruisheng Wang
  • , Yuzheng Zhao
  • , Yi Yang
  • , Jin Huang
  • , David E. Hill
  • , Marc Vidal
  • , Charis Eng
  • , Joseph Loscalzo*
  • *此作品的通讯作者
  • Cleveland Clinic Foundation
  • Case Western Reserve University
  • Hangzhou Normal University
  • Harvard University
  • East China University of Science and Technology
  • Dana-Farber Cancer Institute

科研成果: 期刊稿件文章同行评审

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.

源语言英语
文章编号3476
期刊Nature Communications
10
1
DOI
出版状态已出版 - 1 12月 2019

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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