Evidence map›Paper›PMID 23900022›Full record

ArticleThe Journal of investigative dermatology2014

Matriptase regulates proliferation and early, but not terminal, differentiation of human keratinocytes.

Ya-Wen Chen, Jehng-Kang Wang, Fen-Pai Chou, Bai-Yao Wu, Hui-Chung Hsiao, Han Chiu, Zhonghong Xu, Adrienne N H Baksh, Galen Shi, Malvika Kaul and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Iripin-3, a New Salivary Protein Isolated FromFrontiers in immunology · 2021
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Matriptase expression and zymogen activation in human pilosebaceous unit.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2014
    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

14 authors at 6 institutions in 2 countries.

Ya-Wen ChenGreenebaum Cancer Center, University of Maryland, Baltimore, Maryland, USA; Graduate Program in Life Science, University of Maryland, Baltimore, Maryland, USA.
Jehng-Kang WangDepartment of Biochemistry, National Defense Medical Center, Taipei, Taiwan.
Fen-Pai ChouGreenebaum Cancer Center, University of Maryland, Baltimore, Maryland, USA.
Bai-Yao WuDepartment of Dermatology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Hui-Chung HsiaoDepartment of Biochemistry, National Defense Medical Center, Taipei, Taiwan.
Han ChiuDepartment of Biochemistry, National Defense Medical Center, Taipei, Taiwan.
Zhonghong XuGreenebaum Cancer Center, University of Maryland, Baltimore, Maryland, USA.
Adrienne N H BakshDepartment of Medicine, University of Illinois in Chicago, Chicago, Illinois, USA.
Galen ShiG/T Intern/Mentor Program, Wilde Lake High School, Columbia, Maryland, USA.
Malvika KaulDepartment of Pharmacology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, New Jersey, USA.
Robert BarndtLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Victoria K ShanmugamDepartment of Medicine, Division of Rheumatology, Immunology and Allergy, MedStar Georgetown University Hospital, Washington, DC, USA.
Michael D JohnsonLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Chen-Yong LinLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. Electronic address: lincy@georgetown.edu.
Georgetown University · USNational Defense Medical Center · TWUniversity of Maryland, Baltimore · USRutgers, The State University of New Jersey · USTri-Service General Hospital · TWUniversity of Illinois Chicago · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
Georgetown-Howard Universities Center for Clinical and Translational Science (GHUUL1TR000101 · NCATS · GEORGETOWN UNIVERSITY · PI MELLMAN, THOMAS A, VERBALIS, JOSEPH G · 2012 to 2015
$19.3M
Georgetown-Howard Universities Center for Clinical and Translational Science (GHUUL1RR031975 · NCRR · GEORGETOWN UNIVERSITY · PI VERBALIS, JOSEPH G · 2010 to 2011
$14.6M
Genomics, Biomarkers and Mechanisms of Healing in Chronic WoundsR01NR013888 · NINR · GEORGE WASHINGTON UNIVERSITY · PI SHANMUGAM, VICTORIA KATE · 2012 to 2016
$1.9M
Mechanisms of Deregulation of Matriptase in Breast CancerR01CA123223 · NCI · GEORGETOWN UNIVERSITY · PI JOHNSON, MICHAEL D, LIN, CHEN-YONG · 2010 to 2014
$1.6M
Georgetown-Howard Universities Center for Clinical and Translational Science (GHUKL2RR031974 · NCRR · GEORGETOWN UNIVERSITY · PI VERBALIS, JOSEPH G · 2010 to 2011
$711k
NCATS NIH HHS UL1 TR000101NCATS NIH HHS UL1TR000101NCI NIH HHS P30 CA051008NCI NIH HHS P30-CA051008NCI NIH HHS R01 CA123223NCRR NIH HHS KL2 RR031974NCRR NIH HHS KL2RR031974NCRR NIH HHS UL1 RR031975NCRR NIH HHS UL1RR031975NINR NIH HHS R01 NR013888
6 · The paper itself

Abstract

Genetic defects in matriptase are linked to two congenital ichthyoses: autosomal recessive ichthyosis with hypotrichosis (ARIH, OMIM 610765) and ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis (IFAH, OMIM 602400). Mouse models with matriptase deficiency indicate an involvement of matriptase in suprabasal keratinocytes in the maintenance of the epidermal barrier. In contrast to what has been reported for mouse skin, we show that in human skin matriptase is primarily expressed in the basal and spinous keratinocytes, but not in the more differentiated keratinocytes of the granular layer. In addition, matriptase zymogen activation was predominantly detected in the basal cells. Furthermore, by using skin organotypic cultures as a model system to monitor the course of human epidermal differentiation, we found elevated matriptase zymogen activation during early stages of epidermal differentiation, coupled with a loss of matriptase expression in the late stages of this process. We also show here that matriptase deficiency in HaCaT cells modestly reduces cell proliferation and temporally affects calcium-induced expression of differentiation markers. These collective data suggest that, unlike mouse matriptase, human matriptase may be involved in the regulation of keratinocyte growth and early differentiation, rather than terminal differentiation, providing mechanistic insights into the pathology of the two congenital ichthyoses: ARIH and IFAH.

Indexed as

Cell ProliferationAnimalsCell DifferentiationCell Line, TransformedEpidermal CellsHeterograftsHumansHypotrichosisIchthyosisKeratinocytesMiceMice, KnockoutOrgan Culture TechniquesPrimary Cell CultureSerine EndopeptidasesSerine EndopeptidasesST14 protein, human

Identifiers

PMID23900022
PMCPMC3925676
OpenAlexW2076401425

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.