Author
Listed:
- Feixiong Cheng
(Lerner Research Institute, Cleveland Clinic
Case Western Reserve University
Case Western Reserve University School of Medicine)
- Weiqiang Lu
(East China Normal University)
- Chuang Liu
(Hangzhou Normal University)
- Jiansong Fang
(Lerner Research Institute, Cleveland Clinic)
- Yuan Hou
(Lerner Research Institute, Cleveland Clinic)
- Diane E. Handy
(Harvard Medical School)
- Ruisheng Wang
(Harvard Medical School)
- Yuzheng Zhao
(East China University of Science and Technology
Shanghai Collaborative Innovation Center for Biomanufacturing Technology)
- Yi Yang
(East China University of Science and Technology
Shanghai Collaborative Innovation Center for Biomanufacturing Technology)
- Jin Huang
(East China University of Science and Technology)
- David E. Hill
(Dana-Farber Cancer Institute
Harvard Medical School)
- Marc Vidal
(Dana-Farber Cancer Institute
Harvard Medical School)
- Charis Eng
(Lerner Research Institute, Cleveland Clinic
Case Western Reserve University
Case Western Reserve University School of Medicine
Cleveland Clinic)
- Joseph Loscalzo
(Harvard Medical School)
Abstract
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.
Suggested Citation
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, 2019.
"A genome-wide positioning systems network algorithm for in silico drug repurposing,"
Nature Communications, Nature, vol. 10(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10744-6
DOI: 10.1038/s41467-019-10744-6
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