Evidence map›Paper›PMID 23390516›Full record

ArticlePloS one2013

Occludin is involved in adhesion, apoptosis, differentiation and Ca2+-homeostasis of human keratinocytes: implications for tumorigenesis.

Susanne Rachow, Michaela Zorn-Kruppa, Ulrich Ohnemus, Nina Kirschner, Sabine Vidal-y-Sy, Peter von den Driesch, Christian Börnchen, Jürgen Eberle, Michael Mildner, Eik Vettorazzi and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Contribution of Keratinocytes in Skin Cancer Initiation and Progression.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Review
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  10. Review
  11. Article
  12. Article
  13. Article
  14. Roles of NaWorld journal of gastroenterology · 2019
    Review
  15. Low Expression of Occludin in the Melanoma Patient.Iranian journal of pathology · 2019
    Article
  16. Bicellular Tight Junctions and Wound Healing.International journal of molecular sciences · 2018
    Review
  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

13 authors at 5 institutions in 2 countries.

Susanne RachowDepartment of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Michaela Zorn-Kruppa
Ulrich Ohnemus
Nina Kirschner
Sabine Vidal-y-Sy
Peter von den Driesch
Christian Börnchen
Jürgen Eberle
Michael Mildner
Eik Vettorazzi
Rita Rosenthal
Ingrid Moll
Johanna M Brandner
University Medical Center Hamburg-Eppendorf · DEUniversität Hamburg · DECharité - Universitätsmedizin Berlin · DEKlinikum Stuttgart · DEMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tight junction (TJ) proteins are involved in a number of cellular functions, including paracellular barrier formation, cell polarization, differentiation, and proliferation. Altered expression of TJ proteins was reported in various epithelial tumors. Here, we used tissue samples of human cutaneous squamous cell carcinoma (SCC), its precursor tumors, as well as sun-exposed and non-sun-exposed skin as a model system to investigate TJ protein alteration at various stages of tumorigenesis. We identified that a broader localization of zonula occludens protein (ZO)-1 and claudin-4 (Cldn-4) as well as downregulation of Cldn-1 in deeper epidermal layers is a frequent event in all the tumor entities as well as in sun-exposed skin, suggesting that these changes result from chronic UV irradiation. In contrast, SCC could be distinguished from the precursor tumors and sun-exposed skin by a frequent complete loss of occludin (Ocln). To elucidate the impact of down-regulation of Ocln, we performed Ocln siRNA experiments in human keratinocytes and uncovered that Ocln downregulation results in decreased epithelial cell-cell adhesion and reduced susceptibility to apoptosis induction by UVB or TNF-related apoptosis-inducing ligand (TRAIL), cellular characteristics for tumorigenesis. Furthermore, an influence on epidermal differentiation was observed, while there was no change of E-cadherin and vimentin, markers for epithelial-mesenchymal transition. Ocln knock-down altered Ca(2+)-homeostasis which may contribute to alterations of cell-cell adhesion and differentiation. As downregulation of Ocln is also seen in SCC derived from other tissues, as well as in other carcinomas, we suggest this as a common principle in tumor pathogenesis, which may be used as a target for therapeutic intervention.

Indexed as

AdultAgedAged, 80 and overCalciumCarcinoma, Squamous CellCell AdhesionCell DifferentiationCell Transformation, NeoplasticClaudinsEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHomeostasisHumansKeratinocytesMaleCalciumClaudinsOccludinOCLN protein, humanRNA, Small InterferingTJP1 protein, humanZonula Occludens-1 Protein

Identifiers

PMID23390516
PMCPMC3563667
OpenAlexW2068390416

What OpenQuestion holds

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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.