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A YAP-centered mechanotransduction loop drives collective breast cancer cell invasion

Author

Listed:
  • Antoine A. Khalil

    (University Medical Center Utrecht)

  • Daan Smits

    (University Medical Center Utrecht)

  • Peter D. Haughton

    (University Medical Center Utrecht)

  • Thijs Koorman

    (University Medical Center Utrecht)

  • Karin A. Jansen

    (University Medical Center Utrecht)

  • Mathijs P. Verhagen

    (Erasmus Medical Center)

  • Mirjam Net

    (University Medical Center Utrecht)

  • Kitty Zwieten

    (University Medical Center Utrecht)

  • Lotte Enserink

    (University Medical Center Utrecht)

  • Lisa Jansen

    (University Medical Center Utrecht)

  • Abdelrahman G. El-Gammal

    (University Medical Center Utrecht)

  • Daan Visser

    (University Medical Center Utrecht)

  • Milena Pasolli

    (University Medical Center Utrecht)

  • Max Tak

    (University Medical Center Utrecht)

  • Denise Westland

    (University Medical Center Utrecht)

  • Paul J. Diest

    (University Medical Center Utrecht)

  • Cathy B. Moelans

    (University Medical Center Utrecht)

  • M. Guy Roukens

    (University Medical Center Utrecht
    University Medical Center Utrecht)

  • Sandra Tavares

    (Universidade do Porto)

  • Anne-Marie Fortier

    (Goodman Cancer Institute)

  • Morag Park

    (Goodman Cancer Institute)

  • Riccardo Fodde

    (Erasmus Medical Center)

  • Martijn Gloerich

    (University Medical Center Utrecht)

  • Fried. J. T. Zwartkruis

    (University Medical Center Utrecht)

  • Patrick WB. Derksen

    (University Medical Center Utrecht)

  • Johan Rooij

    (University Medical Center Utrecht)

Abstract

Dense and aligned Collagen I fibers are associated with collective cancer invasion led by protrusive tumor cells, leader cells. In some breast tumors, a population of cancer cells (basal-like cells) maintain several epithelial characteristics and express the myoepithelial/basal cell marker Keratin 14 (K14). Emergence of leader cells and K14 expression are regarded as interconnected events triggered by Collagen I, however the underlying mechanisms remain unknown. Using breast carcinoma organoids, we show that Collagen I drives a force-dependent loop, specifically in basal-like cancer cells. The feed-forward loop is centered around the mechanotransducer Yap and independent of K14 expression. Yap promotes a transcriptional program that enhances Collagen I alignment and tension, which further activates Yap. Active Yap is detected in invading breast cancer cells in patients and required for collective invasion in 3D Collagen I and in the mammary fat pad of mice. Our work uncovers an essential function for Yap in leader cell selection during collective cancer invasion.

Suggested Citation

  • Antoine A. Khalil & Daan Smits & Peter D. Haughton & Thijs Koorman & Karin A. Jansen & Mathijs P. Verhagen & Mirjam Net & Kitty Zwieten & Lotte Enserink & Lisa Jansen & Abdelrahman G. El-Gammal & Daan, 2024. "A YAP-centered mechanotransduction loop drives collective breast cancer cell invasion," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49230-z
    DOI: 10.1038/s41467-024-49230-z
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    References listed on IDEAS

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