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PharmOmics: A Species- and Tissue-specific Drug Signature Database and Online Tool for Drug Repurposing

Yen-Wei Chen, Graciel Diamante, Jessica Ding, Thien Xuan Nghiem, Jessica Yang, Sung-min Ha, Peter Cohn, Douglas Arneson, Montgomery Blencowe, Jennifer Garcia, Nima Zaghari, Paul Patel, Xia Yang
doi: https://doi.org/10.1101/837773
Yen-Wei Chen
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
2Interdepartmental Program of Molecular Toxicology, University of California, Los Angeles, Los Angeles, CA
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Graciel Diamante
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
2Interdepartmental Program of Molecular Toxicology, University of California, Los Angeles, Los Angeles, CA
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Jessica Ding
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
3Interdepartmental Program of Molecular, Cellular, & Integrative Physiology, Los Angeles, Los Angeles, CA
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Thien Xuan Nghiem
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
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Jessica Yang
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
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Sung-min Ha
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
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Peter Cohn
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
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Douglas Arneson
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
4Interdepartmental Program of Bioinformatics, University of California, Los Angeles, Los Angeles, CA
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Montgomery Blencowe
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
3Interdepartmental Program of Molecular, Cellular, & Integrative Physiology, Los Angeles, Los Angeles, CA
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Jennifer Garcia
2Interdepartmental Program of Molecular Toxicology, University of California, Los Angeles, Los Angeles, CA
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Nima Zaghari
2Interdepartmental Program of Molecular Toxicology, University of California, Los Angeles, Los Angeles, CA
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Paul Patel
2Interdepartmental Program of Molecular Toxicology, University of California, Los Angeles, Los Angeles, CA
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Xia Yang
1Department of Integrative Biology and Physiology, University of California, Los Angeles, CA
2Interdepartmental Program of Molecular Toxicology, University of California, Los Angeles, Los Angeles, CA
3Interdepartmental Program of Molecular, Cellular, & Integrative Physiology, Los Angeles, Los Angeles, CA
4Interdepartmental Program of Bioinformatics, University of California, Los Angeles, Los Angeles, CA
5Institute for Quantitative and Computational Biosciences, University of California, Los Angeles, CA
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  • For correspondence: xyang123@ucla.edu
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Abstract

Drug development has been hampered by a high failure rate in clinical trials due to efficacy or safety issues not predicted by preclinical studies in model systems. A key contributor is our incomplete understanding of drug functions across organ systems and species. Therefore, elucidating species- and tissue-specific actions of drugs can provide systems level insights into therapeutic efficacy, potential adverse effects, and interspecies differences that are necessary for more effective translational medicine. Here, we present a comprehensive drug knowledgebase and analytical tool, PharmOmics, comprised of genomic footprints of drugs in individual tissues from human, mouse, and rat transcriptome data from GEO, ArrayExpress, TG-GATEs, and DrugMatrix. Using multi-species and multi-tissue gene expression signatures as molecular indicators of drug functions, we developed gene network-based approaches for drug repositioning. We demonstrate the potential of PharmOmics to predict drugs for new disease indications and validated two predicted drugs for non-alcoholic fatty liver disease in mice. We also examined the potential of PharmOmics to identify drugs related to hepatoxicity and nephrotoxicity. By combining tissue- and species-specific in vivo drug signatures with biological networks, PharmOmics serves as a complementary tool to support drug characterization.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Updated with new drug signatures and new drug toxicity investigation methods.

  • List of abbreviations

    ADR
    adverse drug reactions
    CTD
    comparative toxicogenomics database
    KEGG
    Kyoto Encyclopedia of Genes and Genomes
    DEG
    differential expressed genes
    FDR
    false discovery rate
    wKDA
    weighted key driver analysis
    NAFLD
    non-alcoholic fatty liver disease
    LDL
    low-density lipoprotein cholesterol
    GWAS
    genome-wide association study
    BN
    Bayesian gene regulatory network
    ROC
    Receiver operating characteristic
    HMGCR
    β-Hydroxy β-methylglutaryl-CoA receptor
    PPAR
    Peroxisome proliferator-activated receptor
    GPCR
    G-protein coupled receptor
  • Copyright 
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    Posted March 30, 2021.
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    PharmOmics: A Species- and Tissue-specific Drug Signature Database and Online Tool for Drug Repurposing
    Yen-Wei Chen, Graciel Diamante, Jessica Ding, Thien Xuan Nghiem, Jessica Yang, Sung-min Ha, Peter Cohn, Douglas Arneson, Montgomery Blencowe, Jennifer Garcia, Nima Zaghari, Paul Patel, Xia Yang
    bioRxiv 837773; doi: https://doi.org/10.1101/837773
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    PharmOmics: A Species- and Tissue-specific Drug Signature Database and Online Tool for Drug Repurposing
    Yen-Wei Chen, Graciel Diamante, Jessica Ding, Thien Xuan Nghiem, Jessica Yang, Sung-min Ha, Peter Cohn, Douglas Arneson, Montgomery Blencowe, Jennifer Garcia, Nima Zaghari, Paul Patel, Xia Yang
    bioRxiv 837773; doi: https://doi.org/10.1101/837773

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