Evidence map›Paper›PMID 8983019›Full record

ReviewMolecular biology reports1996

Transcription factor regulation of epidermal keratinocyte gene expression.

R L Eckert, J F Welter

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.7field-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

43 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
  2. Article
  3. Squamous-state excursions activate APOBEC3A in cancer.bioRxiv : the preprint server for biology · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Journal of traditional and complementary medicine · 2019
    Article
  13. Molecular mechanisms of mechanotransduction in psoriasis.Annals of translational medicine · 2018
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

R L EckertDepartment of Physiology, Case Western Reserve University School of Medicine, Cleveland, OH 44106-4970, USA.
J F Welter
University School · US

Funding

Vitamin D endocrine system and Protection Against Skin TumorlgenesisP30AR039750 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI COOPER, KEVIN D · 1988 to 2015
$9.1M
HUMAN INVOLUCRIN GENE REGULATION IN TRANSGENIC MICER01AR041456 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI ECKERT, RICHARD L · 1993 to 2006
$1.2M
INVOLUCRIN AND CORNIFIED ENVELOPE FORMATIONR01GM043751 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI ECKERT, RICHARD L · 1991 to 1998
–
REGULATION OF THE HUMAN INVOLUCRIN GENER55AR041456 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI ECKERT, RICHARD L · 1992 to 1992
–
NIAMS NIH HHS AR39750NIAMS NIH HHS AR41456NIGMS NIH HHS GM43751
6 · The paper itself

Abstract

The epidermis is a tissue that undergoes a very complex and tightly controlled differentiation program. The elaboration of this program is generally flawless, resulting in the production of an effective protective barrier for the organism. Many of the genes expressed during keratinocyte differentiation are expressed in a coordinate manner; this suggests that common regulatory models may emerge. The simplest model envisions a 'common regulatory element' that is possessed by all genes that are regulated together (e.g., involucrin and transglutaminase type 1). Studies to date, however, have not identified any such elements and, if anything, the available studies suggest that appropriate expression of each gene is achieved using sometime subtly and sometime grossly different mechanisms. Recent studies indicate that a variety of transcription factors (AP1, AP2, POU domain. Sp1, STAT factors) are expressed in the epidermis and, in many cases, multiple members of several families are present (e.g., AP1 and POU domain factors). The simultaneous expression of multiple members of a single transcription factor family provides numerous opportunities for complex regulation. Some studies suggest that specific members of these families interact with specific keratinocyte genes. The best studied of these families in epidermis is the AP1 family of factors. All of the known AP1 factors are expressed in epidermis [52] and each is expressed in a specific spatial pattern that suggests the potential to regulate multiple genes. It will be important to determine the role of each of these members in regulating keratinocyte gene expression. Finally, information is beginning to emerge regarding signal transduction in keratinocytes. Some of the early events in signal transduction have been identified (e.g., PLC and PKC activation, etc.) and some of the molecular targets of these pathways (e.g., AP1 transcription factors) are beginning to be identified. Eventually we can expect to elucidation of all of the steps between the interaction of the stimulating agent with its receptor and the activation of target gene expression.

Indexed as

AnimalsCell DivisionDNA-Binding ProteinsEpidermisGene Expression Regulation, DevelopmentalHomeodomain ProteinsHumansKeratinocytesKeratinsMembrane ProteinsProtein Kinase CProtein PrecursorsSignal TransductionSTAT1 Transcription FactorTrans-ActivatorsTranscription Factor AP-1DNA-Binding ProteinsHomeodomain ProteinsHOXB6 protein, humaninvolucrinKeratinsloricrinMembrane ProteinsProtein Kinase CProtein PrecursorsSTAT1 protein, humanSTAT1 Transcription FactorTrans-ActivatorsTranscription Factor AP-1Transcription Factor AP-2Transcription Factors

Identifiers

PMID8983019
OpenAlexW2068908390

What OpenQuestion holds

Textmetadata
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.