Evidence map›Paper›PMID 32270320›Full record

Observational studyArchives of dermatological research2021

The polymorphisms of IL-6/STAT3 signaling pathway may contribute to cutaneous T-cell lymphomas susceptibility.

Berenika Olszewska, Jolanta Gleń, Monika Zabłotna, Roman J Nowicki, Małgorzata Sokołowska-Wojdyło

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Archives of dermatological research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. MicroRNA Regulation of T-Cell Exhaustion in Cutaneous T Cell Lymphoma.The Journal of investigative dermatology · 2022
    Article
  9. Targeted Approaches to T-Cell Lymphoma.Journal of personalized medicine · 2021
    Review
  10. Review
  11. 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

5 authors at 1 institution in 1 country.

Berenika OlszewskaDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Mariana Smoluchowskiego Str 17, 80-214, Gdańsk, Poland. berenika.olszewska@o2.pl.ORCID http://orcid.org/0000-0001-9790-6084
Jolanta GleńDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Mariana Smoluchowskiego Str 17, 80-214, Gdańsk, Poland.
Monika ZabłotnaDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Mariana Smoluchowskiego Str 17, 80-214, Gdańsk, Poland.
Roman J NowickiDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Mariana Smoluchowskiego Str 17, 80-214, Gdańsk, Poland.
Małgorzata Sokołowska-WojdyłoDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Mariana Smoluchowskiego Str 17, 80-214, Gdańsk, Poland.
Gdańsk Medical University · PL

Funding

Polish Ministry of Science and Higher Education ST-66
6 · The paper itself

Abstract

IL-6/STAT3 signaling pathway has been suggested to play a role in CTCL pathogenesis. Polymorphisms in STAT3 signaling pathway-related genes might be a risk factor for CTCL. However, the exact role of inherited gene polymorphisms of IL-6 and STAT3 in the pathogenesis of CTCL is still not fully understood. The aim was to examine whether IL-6 cytokine and polymorphisms of IL-6 and STAT3 gene are associated with CTCL susceptibility, stage of disease and pruritus intensity. We compared the IL-6 serum level and the frequency of selected single nucleotide polymorphisms of IL-6 and STAT3 in 106 CTCL and 198 control group using polymerase chain reaction with sequence-specific primers method and ELISA. We have found that serum IL-6 level in CTCL patients was significantly higher than in healthy controls (p < 0.05). We also demonstrated that two genotypes, CC of IL-6 and GG of STAT3, were overexpressed in CTCL patients compared to healthy controls, and that they increase the risk of malignancy development (OR = 1.8, p = 0.04 for IL-6 and OR 2.53, p = 0.0064 for STAT3). Moreover, the GG genotype of STAT3 polymorphism seems to be associated with lack of pruritus or mild pruritus in CTCL patients. Our results indicate that IL-6 is involved in pathogenesis of CTCL but not pruritus. Moreover, CC of IL-6 and GG genotype of STAT3 genes might be considered as the risk factor for development of CTCL.

Indexed as

AdultAgedAged, 80 and overCase-Control StudiesFemaleGenetic Predisposition to DiseaseHealthy VolunteersHumansInterleukin-6Lymphoma, T-Cell, CutaneousMaleMiddle AgedNeoplasm StagingPolymorphism, Single NucleotidePruritusRisk FactorsIL6 protein, humanInterleukin-6STAT3 protein, humanSTAT3 Transcription FactorCutaneous lymphomasIL-6Mycosis fungoidesPolymorphismSTAT3

Identifiers

PMID32270320
PMCPMC7806529
OpenAlexW3015647087

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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.