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Distinct mesenchymal cell states mediate prostate cancer progression

Author

Listed:
  • Hubert Pakula

    (Weill Cornell Medicine)

  • Mohamed Omar

    (Weill Cornell Medicine
    Weill Cornell Medicine, Belfer Research Building)

  • Ryan Carelli

    (Weill Cornell Medicine)

  • Filippo Pederzoli

    (Weill Cornell Medicine)

  • Giuseppe Nicolò Fanelli

    (Weill Cornell Medicine
    University of Pisa)

  • Tania Pannellini

    (Weill Cornell Medicine)

  • Fabio Socciarelli

    (Weill Cornell Medicine)

  • Lucie Van Emmenis

    (Weill Cornell Medicine)

  • Silvia Rodrigues

    (Weill Cornell Medicine)

  • Caroline Fidalgo-Ribeiro

    (Weill Cornell Medicine)

  • Pier Vitale Nuzzo

    (Weill Cornell Medicine)

  • Nicholas J. Brady

    (Weill Cornell Medicine)

  • Wikum Dinalankara

    (Weill Cornell Medicine)

  • Madhavi Jere

    (Weill Cornell Medicine)

  • Itzel Valencia

    (Weill Cornell Medicine)

  • Christopher Saladino

    (Weill Cornell Medicine)

  • Jason Stone

    (Weill Cornell Medicine)

  • Caitlin Unkenholz

    (Weill Cornell Medicine)

  • Richard Garner

    (Weill Cornell Medicine)

  • Mohammad K. Alexanderani

    (Weill Cornell Medicine)

  • Francesca Khani

    (Weill Cornell Medicine)

  • Francisca Nunes Almeida

    (Columbia University Irving Medical Center)

  • Cory Abate-Shen

    (Columbia University Irving Medical Center
    Columbia University Irving Medical Center
    Columbia University Irving Medical Center
    Columbia University Irving Medical Center)

  • Matthew B. Greenblatt

    (Weill Cornell Medicine)

  • David S. Rickman

    (Weill Cornell Medicine)

  • Christopher E. Barbieri

    (Weill Cornell Medicine, Belfer Research Building
    Weill Cornell Medicine)

  • Brian D. Robinson

    (Weill Cornell Medicine
    Weill Cornell Medicine, Belfer Research Building
    Weill Cornell Medicine)

  • Luigi Marchionni

    (Weill Cornell Medicine)

  • Massimo Loda

    (Weill Cornell Medicine
    Weill Cornell Medicine, Belfer Research Building
    Dana-Farber Cancer Institute and Harvard Medical School
    University of Oxford, Nuffield Department of Surgical Sciences)

Abstract

In the complex tumor microenvironment (TME), mesenchymal cells are key players, yet their specific roles in prostate cancer (PCa) progression remain to be fully deciphered. This study employs single-cell RNA sequencing to delineate molecular changes in tumor stroma that influence PCa progression and metastasis. Analyzing mesenchymal cells from four genetically engineered mouse models (GEMMs) and correlating these findings with human tumors, we identify eight stromal cell populations with distinct transcriptional identities consistent across both species. Notably, stromal signatures in advanced mouse disease reflect those in human bone metastases, highlighting periostin’s role in invasion and differentiation. From these insights, we derive a gene signature that predicts metastatic progression in localized disease beyond traditional Gleason scores. Our results illuminate the critical influence of stromal dynamics on PCa progression, suggesting new prognostic tools and therapeutic targets.

Suggested Citation

  • Hubert Pakula & Mohamed Omar & Ryan Carelli & Filippo Pederzoli & Giuseppe Nicolò Fanelli & Tania Pannellini & Fabio Socciarelli & Lucie Van Emmenis & Silvia Rodrigues & Caroline Fidalgo-Ribeiro & Pie, 2024. "Distinct mesenchymal cell states mediate prostate cancer progression," Nature Communications, Nature, vol. 15(1), pages 1-21, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-023-44210-1
    DOI: 10.1038/s41467-023-44210-1
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    References listed on IDEAS

    as
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