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A YAP-centered mechanotransduction loop drives collective breast cancer cell invasion.
Khalil, Antoine A; Smits, Daan; Haughton, Peter D; Koorman, Thijs; Jansen, Karin A; Verhagen, Mathijs P; van der Net, Mirjam; van Zwieten, Kitty; Enserink, Lotte; Jansen, Lisa; El-Gammal, Abdelrahman G; Visser, Daan; Pasolli, Milena; Tak, Max; Westland, Denise; van Diest, Paul J; Moelans, Cathy B; Roukens, M Guy; Tavares, Sandra; Fortier, Anne-Marie; Park, Morag; Fodde, Riccardo; Gloerich, Martijn; Zwartkruis, Fried J T; Derksen, Patrick Wb; de Rooij, Johan.
Afiliação
  • Khalil AA; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands. a.khalil@umcutrecht.nl.
  • Smits D; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Haughton PD; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Koorman T; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Jansen KA; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Verhagen MP; Department of Pathology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van der Net M; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • van Zwieten K; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Enserink L; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Jansen L; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • El-Gammal AG; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Visser D; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Pasolli M; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Tak M; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Westland D; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • van Diest PJ; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Moelans CB; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Roukens MG; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Tavares S; Regenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Fortier AM; i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
  • Park M; Goodman Cancer Institute McGill University, Depts Biochemistry and Oncology, McGill University, Goodman Cancer Institute, Montréal, Canada.
  • Fodde R; Goodman Cancer Institute McGill University, Depts Biochemistry and Oncology, McGill University, Goodman Cancer Institute, Montréal, Canada.
  • Gloerich M; Department of Pathology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Zwartkruis FJT; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Derksen PW; Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
  • de Rooij J; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands. p.w.b.derksen@umcutrecht.nl.
Nat Commun ; 15(1): 4866, 2024 Jun 07.
Article em En | MEDLINE | ID: mdl-38849373
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Neoplasias da Mama / Colágeno Tipo I / Mecanotransdução Celular / Proteínas Adaptadoras de Transdução de Sinal / Proteínas de Sinalização YAP / Invasividade Neoplásica Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Neoplasias da Mama / Colágeno Tipo I / Mecanotransdução Celular / Proteínas Adaptadoras de Transdução de Sinal / Proteínas de Sinalização YAP / Invasividade Neoplásica Idioma: En Ano de publicação: 2024 Tipo de documento: Article