Evidence map›Paper›PMID 26159543›Full record

ArticleDisease models & mechanisms2015

Suppression of β3-integrin in mice triggers a neuropilin-1-dependent change in focal adhesion remodelling that can be targeted to block pathological angiogenesis.

Tim S Ellison, Samuel J Atkinson, Veronica Steri, Benjamin M Kirkup, Michael E J Preedy, Robert T Johnson, Christiana Ruhrberg, Dylan R Edwards, Jochen G Schneider, Katherine Weilbaecher and 1 more

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Neuropilins in the Context of Tumor Vasculature.International journal of molecular sciences · 2019
    Review
  12. Article
  13. Article
  14. Review
  15. Neuropilin Functions as an Essential Cell Surface Receptor.The Journal of biological chemistry · 2015
    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

11 authors at 5 institutions in 4 countries.

Tim S EllisonSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Samuel J AtkinsonSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Veronica SteriSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Benjamin M KirkupSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Michael E J PreedySchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Robert T JohnsonSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Christiana RuhrbergInstitute of Ophthalmology, University College London, London, EC1V 9EL, UK.
Dylan R EdwardsSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Jochen G SchneiderLuxembourg Center for Systems Biomedicine (LCSB), University of Luxembourg, Luxembourg & Saarland University Medical Center, Internal Medicine II, L-4362 Homburg, Germany.
Katherine WeilbaecherDepartment of Internal Medicine, Division of Molecular Oncology, Washington University in St Louis, St Louis, MO 63110, USA.
Stephen D RobinsonSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK stephen.robinson@uea.ac.uk.
University of East Anglia · GBNorwich Research Park · GBSaarland University · DEUniversity College London · GBWashington University in St. Louis · US

Funding

ROLE OF BETA 3 INTEGRIN IN SKELETAL METASTASISR01CA097250 · NCI · WASHINGTON UNIVERSITY · PI WEILBAECHER, KATHERINE NELSON · 2003 to 2014
$3.3M
NCI NIH HHS R01 CA097250
6 · The paper itself

Abstract

Anti-angiogenic treatments against αvβ3-integrin fail to block tumour growth in the long term, which suggests that the tumour vasculature escapes from angiogenesis inhibition through αvβ3-integrin-independent mechanisms. Here, we show that suppression of β3-integrin in mice leads to the activation of a neuropilin-1 (NRP1)-dependent cell migration pathway in endothelial cells via a mechanism that depends on NRP1's mobilisation away from mature focal adhesions following VEGF-stimulation. The simultaneous genetic targeting of both molecules significantly impairs paxillin-1 activation and focal adhesion remodelling in endothelial cells, and therefore inhibits tumour angiogenesis and the growth of already established tumours. These findings provide a firm foundation for testing drugs against these molecules in combination to treat patients with advanced cancers.

Indexed as

Focal AdhesionsNeovascularization, PathologicAnimalsCell AdhesionCytoplasmCytoskeletonEndothelial CellsFlow CytometryGene Expression ProfilingGene Expression RegulationHeterozygoteHumansIntegrin beta3IntegrinsLungMelanoma, ExperimentalIntegrin beta3IntegrinsKdr protein, mouseNeuropilin-1PaxillinPxn protein, mouseVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2AngiogenesisFocal adhesionIntegrinNeuropilin-1Tumour

Identifiers

PMID26159543
PMCPMC4582102
OpenAlexW2099176027

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Registered trials

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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.