Evidence map›Paper›PMID 27336951›Full record

ArticleNature communications2016

Beta 1-integrin-c-Met cooperation reveals an inside-in survival signalling on autophagy-related endomembranes.

Rachel Barrow-McGee, Naoki Kishi, Carine Joffre, Ludovic Ménard, Alexia Hervieu, Bakhouche A Bakhouche, Alejandro J Noval, Anja Mai, Camilo Guzmán, Luisa Robbez-Masson and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

71 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
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  4. Review
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  7. The role and regulation of integrins in cell migration and invasion.Nature reviews. Molecular cell biology · 2025
    Review
  8. The IPBiochimica et biophysica acta. Molecular basis of disease · 2025
    Article
  9. The MET Oncogene Network of Interacting Cell Surface Proteins.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Autophagy and autophagy-related pathways in cancer.Nature reviews. Molecular cell biology · 2023
    Review
  19. Kindlin-2 controls angiogenesis through modulating Notch1 signaling.Cellular and molecular life sciences : CMLS · 2023
    Article
  20. Emerging roles of the cellular prion protein (PrPCellular and molecular life sciences : CMLS · 2023
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 2 countries.

Rachel Barrow-McGeeSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Naoki KishiSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Carine JoffreSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.ORCID 0000-0002-7551-356X
Ludovic MénardSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Alexia HervieuSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Bakhouche A BakhoucheSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Alejandro J NovalSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Anja MaiUniversity of Turku, Centre for Biotechnology and VTT Technical Research Centre of Finland, FI-20520 Turku, Finland.
Camilo GuzmánUniversity of Turku, Centre for Biotechnology and VTT Technical Research Centre of Finland, FI-20520 Turku, Finland.
Luisa Robbez-MassonSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Xavier IturriozProtein Phosphorylation Laboratory, Francis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
James HulitSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Caroline H BrennanSchool of Biological and Chemical Sciences, Queen Mary University of London, 327 Mile End Road, London E1 4NS, UK.
Ian R HartCentre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Peter J ParkerProtein Phosphorylation Laboratory, Francis Crick Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
Johanna IvaskaUniversity of Turku, Centre for Biotechnology and VTT Technical Research Centre of Finland, FI-20520 Turku, Finland.
Stéphanie KermorgantSpatial Signalling Team, Centre for Tumour Biology, Barts Cancer Institute-A Cancer Research UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK.
Queen Mary University of London · GBUniversity of Turku · FIThe Honourable Society of Lincoln's Inn · GB

Funding

Cancer Research UK 15683European Research Council 615258Medical Research Council G0501003
6 · The paper itself

Abstract

Receptor tyrosine kinases (RTKs) and integrins cooperate to stimulate cell migration and tumour metastasis. Here we report that an integrin influences signalling of an RTK, c-Met, from inside the cell, to promote anchorage-independent cell survival. Thus, c-Met and β1-integrin co-internalize and become progressively recruited on LC3B-positive 'autophagy-related endomembranes' (ARE). In cells growing in suspension, β1-integrin promotes sustained c-Met-dependent ERK1/2 phosphorylation on ARE. This signalling is dependent on ATG5 and Beclin1 but not on ATG13, suggesting ARE belong to a non-canonical autophagy pathway. This β1-integrin-dependent c-Met-sustained signalling on ARE supports anchorage-independent cell survival and growth, tumorigenesis, invasion and lung colonization in vivo. RTK-integrin cooperation has been assumed to occur at the plasma membrane requiring integrin 'inside-out' or 'outside-in' signalling. Our results report a novel mode of integrin-RTK cooperation, which we term 'inside-in signalling'. Targeting integrin signalling in addition to adhesion may have relevance for cancer therapy.

Indexed as

AnimalsAutophagyCarcinogenesisCell AdhesionCell LineCell MovementFibroblastsGene Expression RegulationHepatocyte Growth FactorHumansIntegrin beta1MiceProto-Oncogene Proteins c-metSignal TransductionHepatocyte Growth FactorIntegrin beta1Proto-Oncogene Proteins c-met

Identifiers

PMID27336951
PMCPMC4931016
OpenAlexW2465518274

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.