Evidence map›Paper›PMID 27592801›Full record

ArticleThe Journal of investigative dermatology2017

Foxc1 Ablated Mice Are Anhidrotic and Recapitulate Features of Human Miliaria Sweat Retention Disorder.

Chang-Yi Cui, Ryuga Ishii, Dean P Campbell, Marc Michel, Yulan Piao, Tsutomu Kume, David Schlessinger

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 11 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

7 authors at 2 institutions in 1 country.

Chang-Yi CuiLaboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA. Electronic address: cuic@mail.nih.gov.
Ryuga IshiiLaboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Dean P CampbellLaboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Marc MichelLaboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Yulan PiaoLaboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Tsutomu KumeFeinberg Cardiovascular Research Institute, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
David SchlessingerLaboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
National Institutes of Health · USNorthwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Role Of Ectodysplasin-a In Skin Appendage FormationZIAAG000643 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2018
$7.0M
Fox Transcription factors in lymphatic vessel developmentR01HL126920 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KUME, TSUTOMU · 2015 to 2018
$1.5M
Mechanisms of anterior segment development and corneal neovascularizationR01EY019484 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KUME, TSUTOMU · 2010 to 2014
$1.5M
ROLE OF ECTODYSPLASIN-A IN SKIN APPENDAGES FORMATIONZ01AG000643 · NIA · NATIONAL INSTITUTE ON AGING · PI SCHLESSINGER, DAVID · 1998 to 2008
$1.2M
Intramural NIH HHS Z01 AG000643NCI NIH HHS P30 CA060553NEI NIH HHS R01 EY019484NHLBI NIH HHS R01 HL126920
6 · The paper itself

Abstract

Sweat glands are critical for thermoregulation. The single tubular structure of sweat glands has a lower secretory portion and an upper reabsorptive duct leading to the secretory pore in the skin. Genes that determine sweat gland structure and function are largely unidentified. Here we report that a Fox family transcription factor, Foxc1, is obligate for appreciable sweat duct activity in mice. When Foxc1 was specifically ablated in skin, sweat glands appeared mature, but the mice were severely hypohidrotic. Morphologic analysis revealed that sweat ducts were blocked by hyperkeratotic or parakeratotic plugs. Consequently, lumens in ducts and secretory portions were dilated, and blisters and papules formed on the skin surface in the knockout mice. The phenotype was strikingly similar to the human sweat retention disorder miliaria. We further show that Foxc1 deficiency ectopically induces the expression of keratinocyte terminal differentiation markers in the duct luminal cells, which most likely contribute to keratotic plug formation. Among those differentiation markers, we show that Sprr2a transcription is directly repressed by overexpressed Foxc1 in keratinocytes. In summary, Foxc1 regulates sweat duct luminal cell differentiation, and mutant mice mimic miliaria and provide a possible animal model for its study.

Indexed as

AnimalsBiopsy, NeedleCell DifferentiationCells, CulturedFemaleFluorescent Antibody TechniqueForkhead Transcription FactorsFox-Fordyce DiseaseGene Expression Regulation, DevelopmentalHepatocyte Nuclear Factor 3-alphaHumansHypohidrosisImmunohistochemistryKeratinocytesMiceMice, Inbred C57BLForkhead Transcription FactorsFoxa1 protein, mouseFoxc1 protein, mouseHepatocyte Nuclear Factor 3-alphaRNA, Messenger

Identifiers

PMID27592801
PMCPMC5183533
OpenAlexW2510779983

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.