IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-42354-8.html
   My bibliography  Save this article

Reconstructing disease dynamics for mechanistic insights and clinical benefit

Author

Listed:
  • Amit Frishberg

    (Technion-Israel Institute of Technology
    Helmholtz Center Munich
    Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
    CytoReason)

  • Neta Milman

    (Technion-Israel Institute of Technology)

  • Ayelet Alpert

    (Technion-Israel Institute of Technology)

  • Hannah Spitzer

    (Helmholtz Center Munich
    LMU University Hospital)

  • Ben Asani

    (Ludwig-Maximilians-University)

  • Johannes B. Schiefelbein

    (Ludwig-Maximilians-University)

  • Evgeny Bakin

    (CytoReason)

  • Karen Regev-Berman

    (CytoReason)

  • Siegfried G. Priglinger

    (Ludwig-Maximilians-University)

  • Joachim L. Schultze

    (Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
    University of Bonn
    Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE). PRECISE Platform for Genomics and Epigenomics at DZNE and University of Bonn)

  • Fabian J. Theis

    (Helmholtz Center Munich
    Technical University of Munich
    TUM School of Life Sciences Weihenstephan)

  • Shai S. Shen-Orr

    (Technion-Israel Institute of Technology
    CytoReason)

Abstract

Diseases change over time, both phenotypically and in their underlying molecular processes. Though understanding disease progression dynamics is critical for diagnostics and treatment, capturing these dynamics is difficult due to their complexity and the high heterogeneity in disease development between individuals. We present TimeAx, an algorithm which builds a comparative framework for capturing disease dynamics using high-dimensional, short time-series data. We demonstrate the utility of TimeAx by studying disease progression dynamics for multiple diseases and data types. Notably, for urothelial bladder cancer tumorigenesis, we identify a stromal pro-invasion point on the disease progression axis, characterized by massive immune cell infiltration to the tumor microenvironment and increased mortality. Moreover, the continuous TimeAx model differentiates between early and late tumors within the same tumor subtype, uncovering molecular transitions and potential targetable pathways. Overall, we present a powerful approach for studying disease progression dynamics—providing improved molecular interpretability and clinical benefits for patient stratification and outcome prediction.

Suggested Citation

  • Amit Frishberg & Neta Milman & Ayelet Alpert & Hannah Spitzer & Ben Asani & Johannes B. Schiefelbein & Evgeny Bakin & Karen Regev-Berman & Siegfried G. Priglinger & Joachim L. Schultze & Fabian J. The, 2023. "Reconstructing disease dynamics for mechanistic insights and clinical benefit," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42354-8
    DOI: 10.1038/s41467-023-42354-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-42354-8
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-42354-8?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Ho-Soo Lee & Yong-Yea Park & Mi-Young Cho & Sunyoung Chae & Young-Suk Yoo & Myung-Hee Kwon & Chang-Woo Lee & Hyeseong Cho, 2015. "The chromatin remodeller RSF1 is essential for PLK1 deposition and function at mitotic kinetochores," Nature Communications, Nature, vol. 6(1), pages 1-12, November.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Ho-Soo Lee & Sunwoo Min & Ye-Eun Jung & Sunyoung Chae & June Heo & Jae-Ho Lee & TaeSoo Kim & Ho-Chul Kang & Makoto Nakanish & Sun-Shin Cha & Hyeseong Cho, 2021. "Spatiotemporal coordination of the RSF1-PLK1-Aurora B cascade establishes mitotic signaling platforms," Nature Communications, Nature, vol. 12(1), pages 1-14, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42354-8. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.