Evidence map›Paper›PMID 38849373›Full record

ArticleNature communications2024

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

Antoine A Khalil, Daan Smits, Peter D Haughton, Thijs Koorman, Karin A Jansen, Mathijs P Verhagen, Mirjam van der Net, Kitty van Zwieten, Lotte Enserink, Lisa Jansen and 16 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Antoine A KhalilCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands. a.khalil@umcutrecht.nl.ORCID http://orcid.org/0000-0003-3469-0778
Daan Smits *Center for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-3090-4321
Peter D Haughton *Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Thijs Koorman *Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-6064-3353
Karin A JansenDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Mathijs P VerhagenDepartment of Pathology, Erasmus Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-3126-8379
Mirjam van der NetCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
Kitty van ZwietenCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
Lotte EnserinkDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Lisa JansenCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
Abdelrahman G El-GammalCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
Daan VisserDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-1062-8745
Milena PasolliCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
Max TakCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
Denise WestlandCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.
Paul J van DiestDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0003-0658-2745
Cathy B MoelansDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
M Guy RoukensCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-4270-8678
Sandra Tavaresi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Anne-Marie FortierGoodman Cancer Institute McGill University, Depts Biochemistry and Oncology, McGill University, Goodman Cancer Institute, Montréal, Canada.ORCID http://orcid.org/0000-0002-0428-3066
Morag ParkGoodman Cancer Institute McGill University, Depts Biochemistry and Oncology, McGill University, Goodman Cancer Institute, Montréal, Canada.ORCID http://orcid.org/0000-0001-5400-606X
Riccardo FoddeDepartment of Pathology, Erasmus Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9839-4324
Martijn GloerichCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-0034-4642
Fried J T ZwartkruisCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0001-5775-1313
Patrick Wb DerksenDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands. p.w.b.derksen@umcutrecht.nl.ORCID http://orcid.org/0000-0003-0732-7762
Johan de RooijCenter for Molecular Medicine (CMM), University Medical Center Utrecht, Utrecht, The Netherlands. jderooij@y2y.eu.ORCID http://orcid.org/0000-0001-6101-7875

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 731957
6 · The paper itself

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.

Indexed as

Adaptor Proteins, Signal TransducingBreast NeoplasmsCollagen Type IMechanotransduction, CellularNeoplasm InvasivenessTranscription FactorsYAP-Signaling ProteinsAnimalsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMiceOrganoidsAdaptor Proteins, Signal TransducingCollagen Type ITranscription FactorsYAP1 protein, humanYap1 protein, mouseYAP-Signaling Proteins

Identifiers

PMID38849373
PMCPMC11161601

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.