Evidence map›Paper›PMID 16682529›Full record

ArticleThe Journal of cell biology2006

E-cadherin engagement stimulates proliferation via Rac1.

Wendy F Liu, Celeste M Nelson, Dana M Pirone, Christopher S Chen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

56 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  8. Review
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  11. A central role for cadherin signaling in cancer.Experimental cell research · 2017
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Forms, forces, and stem cell fate.Current opinion in cell biology · 2014
    Review
  18. Article
  19. Article
  20. Article
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

4 authors at 2 institutions in 1 country.

Wendy F LiuDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Celeste M Nelson
Dana M Pirone
Christopher S Chen
Johns Hopkins University · USUniversity of Pennsylvania · US

Funding

REGULATION OF ANGIOGENESIS BY MICROENVIRONMENTAL CUESR01EB000262 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2002 to 2023
$6.2M
Cadherins, integrins, and mechanochemical signalingR01HL073305 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2003 to 2011
$3.4M
Role of Rho-mediated tension in cell proliferationF32HL076060 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI PIRONE, DANA M · 2004 to 2005
$97k
NHLBI NIH HHS F32 HL076060NHLBI NIH HHS HL 076060NHLBI NIH HHS HL73305NHLBI NIH HHS R01 HL073305NIBIB NIH HHS EB00262NIBIB NIH HHS R01 EB000262
6 · The paper itself

Abstract

E-cadherin has been linked to the suppression of tumor growth and the inhibition of cell proliferation in culture. We observed that progressively decreasing the seeding density of normal rat kidney-52E (NRK-52E) or MCF-10A epithelial cells from confluence, indeed, released cells from growth arrest. Unexpectedly, a further decrease in seeding density so that cells were isolated from neighboring cells decreased proliferation. Experiments using microengineered substrates showed that E-cadherin engagement stimulated the peak in proliferation at intermediate seeding densities, and that the proliferation arrest at high densities did not involve E-cadherin, but rather resulted from a crowding-dependent decrease in cell spreading against the underlying substrate. Rac1 activity, which was induced by E-cadherin engagement specifically at intermediate seeding densities, was required for the cadherin-stimulated proliferation, and the control of Rac1 activation by E-cadherin was mediated by p120-catenin. Together, these findings demonstrate a stimulatory role for E-cadherin in proliferative regulation, and identify a simple mechanism by which cell-cell contact may trigger or inhibit epithelial cell proliferation in different settings.

Indexed as

Cell ProliferationAnimalsCadherinsCateninsCell AdhesionCell Adhesion MoleculesCell CommunicationCell CountCell LineCell ShapeContact InhibitionDelta CateninEpithelial CellsHumansModels, BiologicalMutationCadherinsCateninsCell Adhesion MoleculesDelta CateninPhosphoproteinsrac1 GTP-Binding ProteinRNA, Small Interfering

Identifiers

PMID16682529
PMCPMC2063843
OpenAlexW2117852044

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.