Evidence map›Paper›PMID 25482622›Full record

ReviewCell adhesion & migration2014

Eph receptor and ephrin function in breast, gut, and skin epithelia.

Bethany E Perez White, Spiro Getsios

Open access · goldAbstract readReview
In one paragraph

Review in Cell adhesion & migration, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

52 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. EphB4 and ephrin-B1 expression in the intra-testicular-resident macrophages in mice.Journal of advanced veterinary and animal research · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. The EPH/Ephrin System in Colorectal Cancer.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Eph signaling is regulated by miRNA-210: Implications for corneal epithelial repair.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  19. Review
  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

2 authors at 1 institution in 2 countries.

Bethany E Perez Whitea Departments of Dermatology ; Northwestern University ; Chicago , IL USA.
Spiro Getsios
Northwestern University · US

Funding

The Role of Keratinocytes as Independent ThermosensorsP30AR057216 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PALLER, AMY S · 2009 to 2018
$6.0M
Post Graduate Program in Cutaneous BiologyT32AR060710 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Amy S Paller · 2012 to 2026
$2.4M
EphA/Ephrin-A signaling in epidermal differentiation and diseaseR01AR062110 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LAVKER, ROBERT M · 2012 to 2016
$1.9M
NIAMS NIH HHS AR057216NIAMS NIH HHS AR062110NIAMS NIH HHS R01 AR062110NIAMS NIH HHS T32 AR060710
6 · The paper itself

Abstract

Epithelial cells are tightly coupled together through specialized intercellular junctions, including adherens junctions, desmosomes, tight junctions, and gap junctions. A growing body of evidence suggests epithelial cells also directly exchange information at cell-cell contacts via the Eph family of receptor tyrosine kinases and their membrane-associated ephrin ligands. Ligand-dependent and -independent signaling via Eph receptors as well as reverse signaling through ephrins impact epithelial tissue homeostasis by organizing stem cell compartments and regulating cell proliferation, migration, adhesion, differentiation, and survival. This review focuses on breast, gut, and skin epithelia as representative examples for how Eph receptors and ephrins modulate diverse epithelial cell responses in a context-dependent manner. Abnormal Eph receptor and ephrin signaling is implicated in a variety of epithelial diseases raising the intriguing possibility that this cell-cell communication pathway can be therapeutically harnessed to normalize epithelial function in pathological settings like cancer or chronic inflammation.

Indexed as

Cell CommunicationSignal TransductionAnimalsBreast NeoplasmsCell DifferentiationCell ProliferationEphrinsEpithelial CellsGastrointestinal DiseasesHomeostasisHumansMiceReceptors, Eph FamilySkin DiseasesEphrinsReceptors, Eph FamilyADAM, a disintegrin and metalloproteaseApc, adenomatous polyposis coliBreastcell-cellEph, erythropoietin-producing hepatocellularEph receptorephrinepithelialER, estrogen receptorErk, extracellular signal-regulated kinaseGEF, guanine nucleotide exchange factorGPI, glycosylphosphatidylinositolHER2, human epidermal growth factor receptor 2HGF, hepatocyte growth factorIBD, inflammatory bowel diseaseintestineKLF, Krüppel-like factorMAPK, mitogen-activated protein kinaseMMTV-LTR, mouse mammary tumor virus-long terminal repeatMT1-MMP, membrane-type 1 matrix metalloproteinasePDZ, postsynaptic density protein 95, discs large 1, and zonula occludens-1PTP, protein tyrosine phosphatasereceptor tyrosine kinaseRTK, receptor tyrosine kinaseSH2, Src homology 2SHIP2, SH2 inositol phosphatase 2skinSLAP, Src-like adaptor proteinstem cellTCF, T-cell specific transcription factorTEB, terminal end budTNFα, tumor necrosis factor α.

Identifiers

PMID25482622
PMCPMC4594571
OpenAlexW2078900632

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.