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Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension

Author

Listed:
  • Patrick Wu

    (Vanderbilt University Medical Center
    Vanderbilt University School of Medicine)

  • QiPing Feng

    (Vanderbilt University Medical Center)

  • Vern Eric Kerchberger

    (Vanderbilt University Medical Center
    Vanderbilt University Medical Center)

  • Scott D. Nelson

    (Vanderbilt University Medical Center)

  • Qingxia Chen

    (Vanderbilt University Medical Center
    Vanderbilt University School of Medicine)

  • Bingshan Li

    (Vanderbilt University School of Medicine
    Vanderbilt University Medical Center)

  • Todd L. Edwards

    (Vanderbilt University Medical Center
    Tennessee Valley Healthcare System (626)/Vanderbilt University
    Vanderbilt University Medical Center
    Vanderbilt University Medical Center)

  • Nancy J. Cox

    (Vanderbilt University Medical Center
    Vanderbilt University Medical Center)

  • Elizabeth J. Phillips

    (Vanderbilt University Medical Center
    Vanderbilt University School of Medicine
    Vanderbilt University Medical Center
    Murdoch University)

  • C. Michael Stein

    (Vanderbilt University Medical Center
    Vanderbilt University Medical Center
    Vanderbilt University School of Medicine)

  • Dan M. Roden

    (Vanderbilt University Medical Center
    Vanderbilt University Medical Center
    Vanderbilt University School of Medicine)

  • Joshua C. Denny

    (National Institutes of Health
    National Institutes of Health)

  • Wei-Qi Wei

    (Vanderbilt University Medical Center)

Abstract

Discovering novel uses for existing drugs, through drug repurposing, can reduce the time, costs, and risk of failure associated with new drug development. However, prioritizing drug repurposing candidates for downstream studies remains challenging. Here, we present a high-throughput approach to identify and validate drug repurposing candidates. This approach integrates human gene expression, drug perturbation, and clinical data from publicly available resources. We apply this approach to find drug repurposing candidates for two diseases, hyperlipidemia and hypertension. We screen >21,000 compounds and replicate ten approved drugs. We also identify 25 (seven for hyperlipidemia, eighteen for hypertension) drugs approved for other indications with therapeutic effects on clinically relevant biomarkers. For five of these drugs, the therapeutic effects are replicated in the All of Us Research Program database. We anticipate our approach will enable researchers to integrate multiple publicly available datasets to identify high priority drug repurposing opportunities for human diseases.

Suggested Citation

  • Patrick Wu & QiPing Feng & Vern Eric Kerchberger & Scott D. Nelson & Qingxia Chen & Bingshan Li & Todd L. Edwards & Nancy J. Cox & Elizabeth J. Phillips & C. Michael Stein & Dan M. Roden & Joshua C. D, 2022. "Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-021-27751-1
    DOI: 10.1038/s41467-021-27751-1
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    References listed on IDEAS

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    1. Yukinori Okada & Di Wu & Gosia Trynka & Towfique Raj & Chikashi Terao & Katsunori Ikari & Yuta Kochi & Koichiro Ohmura & Akari Suzuki & Shinji Yoshida & Robert R. Graham & Arun Manoharan & Ward Ortman, 2014. "Genetics of rheumatoid arthritis contributes to biology and drug discovery," Nature, Nature, vol. 506(7488), pages 376-381, February.
    2. Dorothée Diogo & Chao Tian & Christopher S. Franklin & Mervi Alanne-Kinnunen & Michael March & Chris C. A. Spencer & Ciara Vangjeli & Michael E. Weale & Hannele Mattsson & Elina Kilpeläinen & Patrick , 2018. "Phenome-wide association studies across large population cohorts support drug target validation," Nature Communications, Nature, vol. 9(1), pages 1-13, December.
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    1. Xiaoguang Xu & Chachrit Khunsriraksakul & James M. Eales & Sebastien Rubin & David Scannali & Sushant Saluja & David Talavera & Havell Markus & Lida Wang & Maciej Drzal & Akhlaq Maan & Abigail C. Lay , 2024. "Genetic imputation of kidney transcriptome, proteome and multi-omics illuminates new blood pressure and hypertension targets," Nature Communications, Nature, vol. 15(1), pages 1-29, December.
    2. Marcin Pilarczyk & Mehdi Fazel-Najafabadi & Michal Kouril & Behrouz Shamsaei & Juozas Vasiliauskas & Wen Niu & Naim Mahi & Lixia Zhang & Nicholas A. Clark & Yan Ren & Shana White & Rashid Karim & Huan, 2022. "Connecting omics signatures and revealing biological mechanisms with iLINCS," Nature Communications, Nature, vol. 13(1), pages 1-13, December.

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