Evidence map›Paper›PMID 11716761›Full record

ArticleThe Biochemical journal2001

The p85 subunit of phosphoinositide 3-kinase is associated with beta-catenin in the cadherin-based adhesion complex.

R J Woodfield, M N Hodgkin, N Akhtar, M A Morse, K J Fuller, K Saqib, N T Thompson, M J Wakelam

Open access · greenAbstract read
In one paragraph

Article in The Biochemical journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 47 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

R J WoodfieldInstitute for Cancer Studies, University of Birmingham, Edgbaston, Birmingham B15 2TA, U.K.
M N Hodgkin
N Akhtar
M A Morse
K J Fuller
K Saqib
N T Thompson
M J Wakelam
Cancer Research UK Clinical Trials Unit · GBGlaxoSmithKline (Ireland) · IEUniversity of Warwick · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell adhesion is fundamental to establishing and maintaining the discrete tissues in multicellular organisms. Adhesion must be sufficiently strong to preserve tissue architecture, whilst having the capacity to readily dissociate to permit fundamental processes, such as wound repair, to occur. However, very little is known about the signalling mechanisms involved in temporary down-regulation of cell adhesion to facilitate such processes. Cadherins are the principal mediators of cell-cell adhesion in a wide variety of tissues and species and form multi-protein complexes with cytosolic and cytoskeletal proteins to express their full adhesive capacity. In the present study we report that the p85 subunit of phosphoinositide 3-kinase (PI 3-kinase) is associated with the cadherin-based adhesion complex in human epithelial cells. The interaction of p85 with the complex is via beta-catenin. We also show that the interaction of p85 and beta-catenin is direct, involves the N-terminal Src homology domain 2 of p85 and is regulated by tyrosine phosphorylation. These data suggest that PI 3-kinase may play a role in the functional regulation of the cadherin-based adhesion complex.

Indexed as

Trans-ActivatorsAnimalsbeta CateninCadherinsCatalytic DomainCell AdhesionCell LineChemical PrecipitationCytoskeletal ProteinsDogsEpidermal Growth FactorErbB ReceptorsGlutathione TransferaseHumansKeratinocytesMacromolecular Substancesbeta CateninCadherinsCTNNB1 protein, humanCytoskeletal ProteinsEpidermal Growth FactorErbB ReceptorsGlutathione TransferaseMacromolecular SubstancesPeptide FragmentsPhosphatidylinositol 3-KinasesRecombinant Fusion ProteinsTrans-Activators

Identifiers

PMID11716761
PMCPMC1222233
OpenAlexW2084944508

What OpenQuestion holds

Textmetadata
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.