Evidence map›Paper›PMID 22040910›Full record

ReviewSeminars in cell & developmental biology2012

Eph/ephrin signaling in epidermal differentiation and disease.

Samantha Lin, Bingcheng Wang, Spiro Getsios

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

38 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  3. Review
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  10. Review
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  15. 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
  16. Article
  17. Article
  18. Review
  19. Article
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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

3 authors at 2 institutions in 1 country.

Samantha LinDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Bingcheng Wang
Spiro Getsios
Northwestern University · USCase Western Reserve University · US

Funding

EphA2 kinase in prostate cancerR01CA155676 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2011 to 2016
$1.6M
Akt-EphA2 Crosstalk in Glioma InvasionR01CA152371 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MIAO, HUI, WANG, BINGCHENG · 2010 to 2014
$1.6M
EphA2 Agonists as Novel Inhibitors of Tumor ProgressionR01CA092259 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2002 to 2007
$1.4M
Eph Kinase Signaling In Renal Epithelial CellsR01DK077876 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2008 to 2011
$1.4M
NCI NIH HHS CA92259NCI NIH HHS R01 CA092259NCI NIH HHS R01 CA152371NCI NIH HHS R01 CA155676NIDDK NIH HHS DK077876NIDDK NIH HHS R01 DK077876
6 · The paper itself

Abstract

Eph receptor tyrosine kinases mediate cell-cell communication by interacting with ephrin ligands residing on adjacent cell surfaces. In doing so, these juxtamembrane signaling complexes provide important contextual information about the cellular microenvironment that helps orchestrate tissue morphogenesis and maintain homeostasis. Eph/ephrin signaling has been implicated in various aspects of mammalian skin physiology, with several members of this large family of receptor tyrosine kinases and their ligands present in the epidermis, hair follicles, sebaceous glands, and underlying dermis. This review focuses on the emerging role of Eph receptors and ephrins in epidermal keratinocytes where they can modulate proliferation, migration, differentiation, and death. The activation of Eph receptors by ephrins at sites of cell-cell contact also appears to play a key role in the maturation of intercellular junctional complexes as keratinocytes move out of the basal layer and differentiate in the suprabasal layers of this stratified, squamous epithelium. Furthermore, alterations in the epidermal Eph/ephrin axis have been associated with cutaneous malignancy, wound healing defects and inflammatory skin conditions. These collective observations suggest that the Eph/ephrin cell-cell communication pathway may be amenable to therapeutic intervention for the purpose of restoring epidermal tissue homeostasis and integrity in dermatological disorders.

Indexed as

Cell DifferentiationSignal TransductionAnimalsCell AdhesionCell ProliferationEphrinsEpidermisHumansKeratinocytesReceptors, Eph FamilySkin NeoplasmsWound HealingEphrinsReceptors, Eph Family

Identifiers

PMID22040910
PMCPMC3378995
OpenAlexW2082784193

What OpenQuestion holds

Textmetadata
LicenceTDM
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.