Evidence map›Paper›PMID 33375941›Full record

ArticleBMC research notes2020

Epigenetic mechanisms shape the underlining expression regulatory mechanisms of the STAT3 in multiple sclerosis disease.

Arezoo Hosseini, Zohreh Babaloo, Tohid Gharibi, Navid Shomali, Faroogh Marofi, Vida Hashemi, Hormoz Ayromlou, Milad Asadi, Shima Rahmani, Saeed Noorolyai and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. The role and mechanism of IL‑35 in myasthenia gravis (Review).International journal of molecular medicine · 2026
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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

12 authors at 2 institutions in 1 country.

Arezoo HosseiniStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Zohreh BabalooImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Tohid GharibiStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Navid ShomaliStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Faroogh MarofiDepartment of Immunology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Vida HashemiDepartment of Basic Science, Faculty of Medicine, Maragheh University of Medical Sciences, Maragheh, Iran.
Hormoz AyromlouDepartment of Neurology, Tabriz University of Medical Sciences, Tabriz, Iran.
Milad AsadiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Shima RahmaniImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Saeed NoorolyaiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Dariush ShanehbandiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. baradaranb@tbzmed.ac.ir.
Tabriz University of Medical Sciences · IRUniversity of Maragheh · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesImmunological tolerance is mediated by CD4

resultsIn this study, we investigated the STAT3 methylation and gene expression status in patients with MS. Our study demonstrated that the level of STAT3 methylation decreased in relapsing-remitting MS patient compared to control groups, which the decreases were statistically significant. STAT3 gene expression increased in patient group relative to healthy one, and the increases were found to be statistically significant. According to our findings, it can be suggested that DNA hypermethylation of STAT3 affects the gene expression. In addition, there is a strong and significant negative correlation between the methylation status and mRNA level of STAT3.

Indexed as

Multiple SclerosisSTAT3 Transcription FactorEpigenesis, GeneticHumansTh17 CellsT-Lymphocytes, RegulatorySTAT3 protein, humanSTAT3 Transcription FactorIranMethylationMultiple sclerosisSTAT3

Identifiers

PMID33375941
PMCPMC7771087
OpenAlexW3115271281

What OpenQuestion holds

Textmetadata
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.