Evidence map›Paper›PMID 28098159›Full record

ArticleNature communications2017

Fluid shear stress activates YAP1 to promote cancer cell motility.

Hyun Jung Lee, Miguel F Diaz, Katherine M Price, Joyce A Ozuna, Songlin Zhang, Eva M Sevick-Muraca, John P Hagan, Pamela L Wenzel

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 164 papers.

0numbers the graph read from it
0cells of the map it votes in
164citing papers in PubMed
12.0field-weighted citation impact, top 1% of its field
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

164 citing papers in PubMed, 256 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Mechanobiology of the Hippo-YAP Signaling Network.Cold Spring Harbor perspectives in biology · 2026
    Article
  9. Review
  10. Review
  11. Mechanical interplay between adipose tissues and disease progression.Bioengineering & translational medicine · 2026
    Review
  12. Article
  13. Review
  14. Article
  15. Directed migration of cancer cells: a systems biophysics perspective.Frontiers in cell and developmental biology · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

104 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 1 country.

Hyun Jung LeeChildren's Regenerative Medicine Program, Department of Pediatric Surgery, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
Miguel F DiazChildren's Regenerative Medicine Program, Department of Pediatric Surgery, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
Katherine M PriceDepartment of BioSciences, Rice University, Houston, Texas 77030, USA.
Joyce A OzunaDepartment of BioSciences, Rice University, Houston, Texas 77030, USA.
Songlin ZhangDepartment of Pathology, The University of Texas Medical School, Houston, Texas 77030, USA.
Eva M Sevick-MuracaCenter for Molecular Imaging, The Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
John P HaganVivian L. Smith Department of Neurosurgery, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
Pamela L WenzelChildren's Regenerative Medicine Program, Department of Pediatric Surgery, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.ORCID 0000-0002-4530-015X
Brown Foundation · USRice University · USThe University of Texas at Austin · USThe University of Texas Health Science Center · US

Funding

Identification of biomechanical pathways that promote hematopoiesisK01DK092365 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WENZEL, PAMELA LYNN · 2011 to 2015
$708k
NIDDK NIH HHS K01 DK092365
6 · The paper itself

Abstract

Mechanical stress is pervasive in egress routes of malignancy, yet the intrinsic effects of force on tumour cells remain poorly understood. Here, we demonstrate that frictional force characteristic of flow in the lymphatics stimulates YAP1 to drive cancer cell migration; whereas intensities of fluid wall shear stress (WSS) typical of venous or arterial flow inhibit taxis. YAP1, but not TAZ, is strictly required for WSS-enhanced cell movement, as blockade of YAP1, TEAD1-4 or the YAP1-TEAD interaction reduces cellular velocity to levels observed without flow. Silencing of TEAD phenocopies loss of YAP1, implicating transcriptional transactivation function in mediating force-enhanced cell migration. WSS dictates expression of a network of YAP1 effectors with executive roles in invasion, chemotaxis and adhesion downstream of the ROCK-LIMK-cofilin signalling axis. Altogether, these data implicate YAP1 as a fluid mechanosensor that functions to regulate genes that promote metastasis.

Indexed as

Cell MovementStress, MechanicalActin Depolymerizing FactorsAdaptor Proteins, Signal TransducingAnimalsCell Line, TumorDNA-Binding ProteinsExtracellular FluidHumansLim KinasesLymphatic VesselsMaleMechanotransduction, CellularMiceMice, NudeNeoplasmsActin Depolymerizing FactorsAdaptor Proteins, Signal TransducingDNA-Binding ProteinsLIMK1 protein, humanLim KinasesNuclear ProteinsPhosphoproteinsTEAD1 protein, humanTEAD2 protein, humanTEA Domain Transcription FactorsTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID28098159
PMCPMC5253685
OpenAlexW2572990295

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.