Evidence map›Paper›PMID 31724286›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2020

Interferon regulatory factor 6 is required for proper wound healing in vivo.

Lindsey Rhea, Franklin J Canady, Marc Le, Tanner Reeb, John W Canady, Deborah S F Kacmarynski, Rishika Avvari, Leah C Biggs, Martine Dunnwald

Open access · greenAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2020. 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
1.6field-weighted citation impact, top 15% 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, 15 citations in OpenAlex.

  1. Review
  2. ARHGAP29 promotes keratinocyte proliferation and migration in vitro and is dispensable for in vivo wound healing.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Article
  3. Article
  4. Neural crest and periderm-specific requirements ofbioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. A Novel Van der Woude Syndrome-CausingFrontiers in cell and developmental biology · 2020
    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

9 authors at 1 institution in 1 country.

Lindsey RheaDepartment of Anatomy and Cell Biology, The University of Iowa, Iowa City, Iowa.
Franklin J CanadyDepartment of Pediatrics, The University of Iowa, Iowa City, Iowa.
Marc LeDepartment of Pediatrics, The University of Iowa, Iowa City, Iowa.
Tanner ReebDepartment of Anatomy and Cell Biology, The University of Iowa, Iowa City, Iowa.
John W CanadyDepartment of Otolaryngology, Head and Neck Surgery, The University of Iowa, Iowa City, Iowa.
Deborah S F KacmarynskiDepartment of Pediatrics, The University of Iowa, Iowa City, Iowa.
Rishika AvvariDepartment of Anatomy and Cell Biology, The University of Iowa, Iowa City, Iowa.
Leah C BiggsDepartment of Pediatrics, The University of Iowa, Iowa City, Iowa.
Martine DunnwaldDepartment of Anatomy and Cell Biology, The University of Iowa, Iowa City, Iowa.ORCID 0000-0002-5182-8874
University of Iowa · US

Funding

Molecular Genetic Epidemiology of Cleft Lip and PalateR37DE008559 · NIDCR · UNIVERSITY OF IOWA · PI MURRAY, JEFFREY C · 2004 to 2013
$6.8M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008629 · NIGMS · UNIVERSITY OF IOWA · PI EBERL, DANIEL F · 1997 to 2021
$4.1M
IRF6 and Wound HealingR01AR067739 · NIAMS · UNIVERSITY OF IOWA · PI DUNNWALD, MARTINE · 2016 to 2020
$1.8M
MOLECULAR GENETIC EPIDEMIOLOGY OF CLEFT LIP AND PALATER01DE008559 · NIDCR · UNIVERSITY OF IOWA · PI MURRAY, JEFFREY C · 1988 to 2003
$1.5M
NIAMS NIH HHS R01 AR067739NIDCR NIH HHS R01 DE008559NIDCR NIH HHS R37 DE008559NIGMS NIH HHS T32 GM008629
6 · The paper itself

Abstract

backgroundVan der Woude syndrome (VWS) is the most common form of syndromic orofacial cleft caused predominantly by mutations in Interferon Regulatory Factor 6 (IRF6). We previously reported that individuals with VWS have increased risk of wound healing complications following cleft repair compared with individuals with nonsyndromic orofacial clefts (nonsyndromic cleft lip and palate-NSCLP). In vitro, absence of IRF6 leads to impaired keratinocyte migration and embryonic wound healing. However, there is currently no data on tissue repair in adult animals and cells with reduced levels of IRF6 like in VWS.

resultsExcisional wounds of Irf6

conclusionsThese data support a role for IRF6 in wound healing by regulating keratinocyte proliferation, granulation tissue maturation, and cytokine levels.

Indexed as

AnimalsBlotting, WesternCell CycleCell MovementCell ProliferationCells, CulturedCytokinesHumansInterferon Regulatory FactorsKeratinocytesMice, Inbred C57BLMutationProliferating Cell Nuclear AntigenWound HealingCytokinesInterferon Regulatory FactorsIRF6 protein, mouseProliferating Cell Nuclear AntigencraniofacialkeratinocytesmouseVan der Woude syndromewound healing

Identifiers

PMID31724286
PMCPMC9266192
OpenAlexW2984197558

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.