Evidence map›Paper›PMID 26829034›Full record

ArticleThe Journal of investigative dermatology2016

Ectodysplasin A Pathway Contributes to Human and Murine Skin Repair.

Clare L Garcin, Kenneth M Huttner, Neil Kirby, Pascal Schneider, Matthew J Hardman

Open access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of investigative dermatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. The Role of Ectodysplasin A on the Ocular Surface Homeostasis.International journal of molecular sciences · 2022
    Review
  4. 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

5 authors at 3 institutions in 3 countries.

Clare L GarcinThe Healing Foundation Centre, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Kenneth M HuttnerEdimer Pharmaceuticals Inc, Cambridge, Massachusetts, USA.
Neil KirbyEdimer Pharmaceuticals Inc, Cambridge, Massachusetts, USA.
Pascal SchneiderDepartment of Biochemistry, University of Lausanne, Lausanne, Switzerland.
Matthew J HardmanThe Healing Foundation Centre, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom. Electronic address: Matthew.j.hardman@manchester.ac.uk.
Edimer Pharmaceuticals (United States) · USLGBT Foundation · GBUniversity of Lausanne · CH

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council
6 · The paper itself

Abstract

The highly conserved ectodysplasin A (EDA)/EDA receptor signaling pathway is critical during development for the formation of skin appendages. Mutations in genes encoding components of the EDA pathway disrupt normal appendage development, leading to the human disorder hypohidrotic ectodermal dysplasia. Spontaneous mutations in the murine Eda (Tabby) phenocopy human X-linked hypohidrotic ectodermal dysplasia. Little is known about the role of EDA signaling in adult skin homeostasis or repair. Because wound healing largely mimics the morphogenic events that occur during development, we propose a role for EDA signaling in adult wound repair. Here we report a pronounced delay in healing in Tabby mice, demonstrating a functional role for EDA signaling in adult skin. Moreover, pharmacological activation of the EDA pathway in both Tabby and wild-type mice significantly accelerates healing, influencing multiple processes including re-epithelialization and granulation tissue matrix deposition. Finally, we show that the healing promoting effects of EDA receptor activation are conserved in human skin repair. Thus, targeted manipulation of the EDA/EDA receptor pathway has clear therapeutic potential for the future treatment of human pathological wound healing.

Indexed as

AnimalsBiopsy, NeedleDisease Models, AnimalEctodermal DysplasiaEctodysplasinsEdar ReceptorHumansImmunohistochemistryMaleMiceMice, Inbred C57BLRandom AllocationSensitivity and SpecificitySignal TransductionWound HealingWounds and InjuriesEctodysplasinsEDAR protein, humanEdar protein, mouseEdar Receptor

Identifiers

PMID26829034
PMCPMC4967474
OpenAlexW2262953917

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.