Evidence map›Paper›PMID 28608476›Full record

ArticleThe Journal of pathology2017

Pro-migratory and TGF-β-activating functions of αvβ6 integrin in pancreatic cancer are differentially regulated via an Eps8-dependent GTPase switch.

Jo Tod, Christopher J Hanley, Mark R Morgan, Marta Rucka, Toby Mellows, Maria-Antoinette Lopez, Philip Kiely, Karwan A Moutasim, Steven J Frampton, Durgagauri Sabnis and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Progress in the application ofAnnals of nuclear medicine · 2026
    Review
  2. Article
  3. Integrins as Key Mediators of Metastasis.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Adaptor protein Abelson interactor 1 in homeostasis and disease.Cell communication and signaling : CCS · 2024
    Review
  6. Exploring the role of ITGB6: fibrosis, cancer, and other diseases.Apoptosis : an international journal on programmed cell death · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
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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

16 authors at 4 institutions in 2 countries.

Jo TodCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Christopher J HanleyCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Mark R MorganInstitute of Translational Medicine, University of Liverpool, Crown Street, Liverpool, UK.
Marta RuckaCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Toby MellowsClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Maria-Antoinette LopezCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Philip KielyCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Karwan A MoutasimCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Steven J FramptonCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Durgagauri SabnisCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
David R FineClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Colin JohnsonCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
John F MarshallBarts Cancer Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, UK.
Giorgio ScitaIFOM FOM Foundation, Institute FIRC of Molecular Oncology and University of Milan, School of Medicine, Department of Oncology and Hemato-Oncology-DIPO, Via Adamello, Milan, Italy.
Veronika JeneiCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.ORCID 0000-0002-1996-5676
Gareth J ThomasCancer Sciences Unit, Faculty of Medicine, University of Southampton, Tremona Road, Southampton, UK.
Southampton General Hospital · GBQueen Mary University of London · GBUniversity of Liverpool · GBUniversity of Milan · IT

Funding

Cancer Research UK 20256Cancer Research UK C11512/A20256Medical Research Council G1002008
6 · The paper itself

Abstract

The integrin αvβ6 is up-regulated in numerous carcinomas, where expression commonly correlates with poor prognosis. αvβ6 promotes tumour invasion, partly through regulation of proteases and cell migration, and is also the principal mechanism by which epithelial cells activate TGF-β1; this latter function complicates therapeutic targeting of αvβ6, since TGF-β1 has both tumour-promoting and -suppressive effects. It is unclear how these different αvβ6 functions are linked; both require actin cytoskeletal reorganization, and it is suggested that tractive forces generated during cell migration activate TGF-β1 by exerting mechanical tension on the ECM-bound latent complex. We examined the functional relationship between cell invasion and TGF-β1 activation in pancreatic ductal adenocarcinoma (PDAC) cells, and confirmed that both processes are αvβ6-dependent. Surprisingly, we found that cellular functions could be biased towards either motility or TGF-β1 activation depending on the presence or absence of epidermal growth factor receptor pathway substrate 8 (Eps8), a regulator of actin remodelling, endocytosis, and GTPase activation. Similar to αvβ6, we found that Eps8 was up-regulated in >70% of PDACs. In complex with Abi1/Sos1, Eps8 regulated αvβ6-dependent cell migration through activation of Rac1. Down-regulation of Eps8, Sos1 or Rac1 suppressed cell movement, while simultaneously increasing αvβ6-dependent TGF-β1 activation. This latter effect was modulated through increased cell tension, regulated by Rho activation. Thus, the Eps8/Abi1/Sos1 tricomplex acts as a key molecular switch altering the balance between Rac1 and Rho activation; its presence or absence in PDAC cells modulates αvβ6-dependent functions, resulting in a pro-migratory (Rac1-dependent) or a pro-TGF-β1 activation (Rho-dependent) functional phenotype, respectively. © 2017 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

Cell MovementAdaptor Proteins, Signal TransducingAntigens, NeoplasmCarcinoma, Pancreatic DuctalCell Line, TumorCoculture TechniquesCytoskeletal ProteinsEnzyme InhibitorsHumansIntegrinsNeoplasm InvasivenessPancreatic NeoplasmsPhenotyperac1 GTP-Binding Proteinrho GTP-Binding ProteinsRNA InterferenceABI1 protein, humanAdaptor Proteins, Signal TransducingAntigens, NeoplasmCytoskeletal ProteinsEnzyme InhibitorsEPS8 protein, humanintegrin alphavbeta6Integrinsrac1 GTP-Binding ProteinRAC1 protein, humanrho GTP-Binding ProteinsSOS1 ProteinTGFB1 protein, humanTransforming Growth Factor beta1Eps8motilityRac1RhoTGF-β1αvβ6

Identifiers

PMID28608476
PMCPMC5601247
OpenAlexW2624852477

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.