Evidence map›Paper›PMID 28589370›Full record

ArticleMolecular and cellular biochemistry2017

Splicing factors differentially expressed in psoriasis alter mRNA maturation of disease-associated EDA+ fibronectin.

E Szlavicz, K Szabo, G Groma, Z Bata-Csorgo, F Pagani, L Kemeny, M Szell

Erratum issuedOpen access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Psoriasis, Is It a Microdamage of Our "Sixth Sense"? A Neurocentric View.International journal of molecular sciences · 2022
    Article
  8. Article
  9. Article
  10. Observational
  11. Article
  12. Re-investigating the Basement Membrane Zone of Psoriatic Epidermal Lesions: Is Laminin-511 a New Player in Psoriasis Pathogenesis?The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2018
    Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

E SzlaviczDepartment of Dermatology and Allergology, Faculty of Medicine, University of Szeged, 6 Korányi fasor, Szeged, 6720, Hungary. szlavicz.eszter@gmail.com.ORCID http://orcid.org/0000-0002-1083-0994
K SzaboMTA-SZTE Dermatological Research Group, Szeged, Hungary.
G GromaMTA-SZTE Dermatological Research Group, Szeged, Hungary.
Z Bata-CsorgoDepartment of Dermatology and Allergology, Faculty of Medicine, University of Szeged, 6 Korányi fasor, Szeged, 6720, Hungary.
F PaganiInternational Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
L KemenyDepartment of Dermatology and Allergology, Faculty of Medicine, University of Szeged, 6 Korányi fasor, Szeged, 6720, Hungary.
M SzellMTA-SZTE Dermatological Research Group, Szeged, Hungary.
University of Szeged · HUMTA-SZTE Research Group on Artificial Intelligence · HUInternational Centre for Genetic Engineering and Biotechnology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The EDA+ fibronectin splicing variant is overexpressed in psoriatic non-lesional epidermis and sensitizes keratinocytes to mitogenic signals. However, regulation of its abundance is only partially understood. In our recent cDNA microarray experiment, we identified three SR-rich splicing factors-splicing factor, arginine/serine-rich 18 (SFRS18), peptidyl-prolyl cis-trans isomerase G (PPIG), and luc-7 like protein 3 (LUC7L3)-which might be implicated in the preactivated states of keratinocytes in psoriatic non-involved skin and could also contribute to the regulation of fibronectin mRNA maturation. In this study, we investigated the role of LUC7L3, PPIG, and SFRS18 in psoriasis and in the mRNA maturation process of fibronectin. Regarding tissue staining experiments, we were able to demonstrate a characteristic distribution of the splicing factors in healthy, psoriatic non-involved and involved epidermis. Moreover, the expression profiles of these SR-rich proteins were found to be very similar in synchronized keratinocytes. Contribution of splicing facwwtors to the EDA+ fibronectin formation was also confirmed: their siRNA silencing leads to altered fibronectin mRNA and protein expression patterns, suggesting the participation in the EDA domain inclusion. Our results indicate that LUC7L3, PPIG, and SFRS18 are not only implicated in EDA+ fibronectin formation, but also that they could possess multiple roles in psoriasis-associated molecular abnormalities.

Indexed as

RNA SplicingAdolescentAdultCyclophilinsFemaleFibronectinsHumansKeratinocytesMaleMiddle AgedNuclear ProteinsPsoriasisRNA-Binding ProteinsRNA, MessengerRNA Splicing FactorsCyclophilinsFibronectinsLUC7L3 protein, humanNuclear ProteinsPPIG protein, humanRNA-Binding ProteinsRNA, MessengerRNA Splicing FactorsEDA+ fibronectinmRNA splicingPsoriasisSR-rich splicing factors

Identifiers

PMID28589370
OpenAlexW2622214567

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.