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Biologically informed deep neural network for prostate cancer discovery

Author

Listed:
  • Haitham A. Elmarakeby

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard
    Al-Azhar University)

  • Justin Hwang

    (University of Minnesota, Division of Hematology, Oncology and Transplantation)

  • Rand Arafeh

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

  • Jett Crowdis

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

  • Sydney Gang

    (Dana-Farber Cancer Institute)

  • David Liu

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

  • Saud H. AlDubayan

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

  • Keyan Salari

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard
    Massachusetts General Hospital, Harvard Medical School)

  • Steven Kregel

    (University of Illinois at Chicago)

  • Camden Richter

    (Dana-Farber Cancer Institute)

  • Taylor E. Arnoff

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

  • Jihye Park

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

  • William C. Hahn

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

  • Eliezer M. Van Allen

    (Dana-Farber Cancer Institute
    Broad Institute of MIT and Harvard)

Abstract

The determination of molecular features that mediate clinically aggressive phenotypes in prostate cancer remains a major biological and clinical challenge1,2. Recent advances in interpretability of machine learning models as applied to biomedical problems may enable discovery and prediction in clinical cancer genomics3–5. Here we developed P-NET—a biologically informed deep learning model—to stratify patients with prostate cancer by treatment-resistance state and evaluate molecular drivers of treatment resistance for therapeutic targeting through complete model interpretability. We demonstrate that P-NET can predict cancer state using molecular data with a performance that is superior to other modelling approaches. Moreover, the biological interpretability within P-NET revealed established and novel molecularly altered candidates, such as MDM4 and FGFR1, which were implicated in predicting advanced disease and validated in vitro. Broadly, biologically informed fully interpretable neural networks enable preclinical discovery and clinical prediction in prostate cancer and may have general applicability across cancer types.

Suggested Citation

  • Haitham A. Elmarakeby & Justin Hwang & Rand Arafeh & Jett Crowdis & Sydney Gang & David Liu & Saud H. AlDubayan & Keyan Salari & Steven Kregel & Camden Richter & Taylor E. Arnoff & Jihye Park & Willia, 2021. "Biologically informed deep neural network for prostate cancer discovery," Nature, Nature, vol. 598(7880), pages 348-352, October.
  • Handle: RePEc:nat:nature:v:598:y:2021:i:7880:d:10.1038_s41586-021-03922-4
    DOI: 10.1038/s41586-021-03922-4
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    Cited by:

    1. Erik Hartman & Aaron M. Scott & Christofer Karlsson & Tirthankar Mohanty & Suvi T. Vaara & Adam Linder & Lars Malmström & Johan Malmström, 2023. "Interpreting biologically informed neural networks for enhanced proteomic biomarker discovery and pathway analysis," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    2. Winn-Nuñez, Emily T. & Griffin, Maryclare & Crawford, Lorin, 2024. "A simple approach for local and global variable importance in nonlinear regression models," Computational Statistics & Data Analysis, Elsevier, vol. 194(C).
    3. Md Tauhidul Islam & Zixia Zhou & Hongyi Ren & Masoud Badiei Khuzani & Daniel Kapp & James Zou & Lu Tian & Joseph C. Liao & Lei Xing, 2023. "Revealing hidden patterns in deep neural network feature space continuum via manifold learning," Nature Communications, Nature, vol. 14(1), pages 1-20, December.

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