Evidence map›Paper›PMID 28636467›Full record

ArticleSmall GTPases2019

Normal epithelial cells trigger EphA2-dependent RasV12 cell repulsion at the single cell level.

William Hill, Catherine Hogan

Open access · hybridAbstract read
In one paragraph

Article in Small GTPases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

12 citing papers in PubMed, 19 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

2 authors at 1 institution in 1 country.

William Hilla European Cancer Stem Cell Research Institute, School of Biosciences , Cardiff University , Cardiff , UK.
Catherine Hogana European Cancer Stem Cell Research Institute, School of Biosciences , Cardiff University , Cardiff , UK.ORCID 0000-0002-1012-0896
Cardiff University · GB

Funding

Medical Research Council
6 · The paper itself

Abstract

Epithelial cells expressing oncogenic Ras (RasV12) are detected by normal neighbors and are often extruded from tissues. We recently demonstrated that differential EphA2 signaling drives the segregation of mutant cells from normal monolayers via cell repulsion and increased RasV12 cell contractility. EphA2 signaling on RasV12 cells is triggered by ephrin-A ligands presented by normal cells. Here, we show that normal epithelial cells trigger the repulsion and enhanced contractility of Ras-transformed epithelial cells at the single cell level. We also reveal that ephrin-A ligands expressed on RasV12 cells are not required to drive RasV12 cell segregation following interaction with normal cells. Thus, normal-RasV12 cell-cell interaction triggers EphA2 forward signaling in RasV12 cells to drive repulsion and segregation of the transformed cells.

Indexed as

AnimalsCell CommunicationCell LineCoculture TechniquesDogsEpithelial CellsMadin Darby Canine Kidney CellsMutationras ProteinsReceptor, EphA2Signal TransductionSingle-Cell AnalysisTransformation, Geneticras ProteinsReceptor, EphA2cell repulsionEphA2epithelialextrusionRasV12single cell

Identifiers

PMID28636467
PMCPMC6548300
OpenAlexW2621894369

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.