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MYC Deregulation and PTEN Loss Model Tumor and Stromal Heterogeneity of Aggressive Triple-Negative Breast Cancer

Author

Listed:
  • Zinab O. Doha

    (Oregon Health & Science University
    Taibah University)

  • Xiaoyan Wang

    (Oregon Health & Science University)

  • Nicholas L. Calistri

    (Oregon Health & Science University)

  • Jennifer Eng

    (Oregon Health & Science University
    Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University)

  • Colin J. Daniel

    (Oregon Health & Science University)

  • Luke Ternes

    (Oregon Health & Science University)

  • Eun Na Kim

    (Oregon Health & Science University)

  • Carl Pelz

    (Oregon Health & Science University
    Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University)

  • Michael Munks

    (Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University
    Oregon Health and Science University)

  • Courtney Betts

    (Oregon Health and Science University)

  • Sunjong Kwon

    (Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University)

  • Elmar Bucher

    (Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University)

  • Xi Li

    (Division of Oncologic Sciences, Oregon Health and Science University)

  • Trent Waugh

    (Oregon Health & Science University)

  • Zuzana Tatarova

    (Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University)

  • Dylan Blumberg

    (Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University)

  • Aaron Ko

    (Oregon Health and Science University)

  • Nell Kirchberger

    (Oregon Health and Science University)

  • Jennifer A. Pietenpol

    (Vanderbilt University Medical Center
    Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center)

  • Melinda E. Sanders

    (Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center
    Vanderbilt University Medical Center)

  • Ellen M. Langer

    (Oregon Health & Science University)

  • Mu-Shui Dai

    (Oregon Health & Science University)

  • Gordon Mills

    (Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University
    Division of Oncologic Sciences, Oregon Health and Science University
    Knight Cancer Institute, Oregon Health & Science University)

  • Koei Chin

    (Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University
    Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University
    Knight Cancer Institute, Oregon Health & Science University)

  • Young Hwan Chang

    (Oregon Health & Science University
    Knight Cancer Institute, Oregon Health & Science University)

  • Lisa M. Coussens

    (Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University
    Oregon Health and Science University
    Knight Cancer Institute, Oregon Health & Science University)

  • Joe W. Gray

    (Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University
    Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University
    Knight Cancer Institute, Oregon Health & Science University)

  • Laura M. Heiser

    (Oregon Health & Science University
    OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University
    Knight Cancer Institute, Oregon Health & Science University)

  • Rosalie C. Sears

    (Oregon Health & Science University
    Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University
    Knight Cancer Institute, Oregon Health & Science University)

Abstract

Triple-negative breast cancer (TNBC) patients have a poor prognosis and few treatment options. Mouse models of TNBC are important for development of new therapies, however, few mouse models represent the complexity of TNBC. Here, we develop a female TNBC murine model by mimicking two common TNBC mutations with high co-occurrence: amplification of the oncogene MYC and deletion of the tumor suppressor PTEN. This Myc;Ptenfl model develops heterogeneous triple-negative mammary tumors that display histological and molecular features commonly found in human TNBC. Our research involves deep molecular and spatial analyses on Myc;Ptenfl tumors including bulk and single-cell RNA-sequencing, and multiplex tissue-imaging. Through comparison with human TNBC, we demonstrate that this genetic mouse model develops mammary tumors with differential survival and therapeutic responses that closely resemble the inter- and intra-tumoral and microenvironmental heterogeneity of human TNBC, providing a pre-clinical tool for assessing the spectrum of patient TNBC biology and drug response.

Suggested Citation

  • Zinab O. Doha & Xiaoyan Wang & Nicholas L. Calistri & Jennifer Eng & Colin J. Daniel & Luke Ternes & Eun Na Kim & Carl Pelz & Michael Munks & Courtney Betts & Sunjong Kwon & Elmar Bucher & Xi Li & Tre, 2023. "MYC Deregulation and PTEN Loss Model Tumor and Stromal Heterogeneity of Aggressive Triple-Negative Breast Cancer," Nature Communications, Nature, vol. 14(1), pages 1-21, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40841-6
    DOI: 10.1038/s41467-023-40841-6
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    References listed on IDEAS

    as
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    4. Charles M. Perou & Therese Sørlie & Michael B. Eisen & Matt van de Rijn & Stefanie S. Jeffrey & Christian A. Rees & Jonathan R. Pollack & Douglas T. Ross & Hilde Johnsen & Lars A. Akslen & Øystein Flu, 2000. "Molecular portraits of human breast tumours," Nature, Nature, vol. 406(6797), pages 747-752, August.
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