Evidence map›Paper›PMID 38948276›Full record

ArticleSichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition2024

[H3K27me3 Expression Level and Its Epigenetic Regulation Mechanisms in Th17 Cell Differentiation in Patients With Ankylosing Spondylitis].

Ming Cheng, Long Jia, Zhiyuan Xue, Tao Yang, Xue Zhou, Guanlan Zhao

Abstract readEnglish Abstract
In one paragraph

Article in Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Ming Cheng( 610036) Department of Rehabilitation, Jinniu District People's Hospital of Chengdu, Chengdu 610036, China.
Long Jia( 610036) Department of Rehabilitation, Jinniu District People's Hospital of Chengdu, Chengdu 610036, China.
Zhiyuan Xue( 610036) Department of Rehabilitation, Jinniu District People's Hospital of Chengdu, Chengdu 610036, China.
Tao Yang( 610036) Department of Rehabilitation, Jinniu District People's Hospital of Chengdu, Chengdu 610036, China.
Xue Zhou( 610036) Department of Rehabilitation, Jinniu District People's Hospital of Chengdu, Chengdu 610036, China.
Guanlan Zhao( 610036) Department of Rehabilitation, Jinniu District People's Hospital of Chengdu, Chengdu 610036, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To investigate the roles of histone H3K27me3 methylation and its regulatory enzymes JMJD3 and EZH2 in the differentiation of Th17 cells in ankylosing spondylitis (AS), to unveil their potential involvement in the pathogenesis of AS, and to provide new strategies and targets for the clinical treatment of AS by analyzing the methylation state of H3K27me3 and its interactions with Th17-related factors. Methods: A total of 84 AS patients (42 active AS patiens and 42 patients in the stable phase of AS) were enrolled for the study, while 84 healthy volunteers were enrolled as the controls. Blood samples were collected. Peripheral blood mononuclear cells were isolated. ELISA assay was performed to examine Th17 cells and the relevant cytokines IL-21, IL-22, and IL-17. The mRNA expressions of Results: The mRNA expressions of Conclusion: The low expression of H3K27me3 in AS is influenced by the gene loci JMJD3 and EZH2, which can regulate the differentiation of Th17 cells and thus play a role in the pathogenesis and progression of AS.

Indexed as

Cell DifferentiationEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticHistonesInterleukin-17Jumonji Domain-Containing Histone DemethylasesNuclear Receptor Subfamily 1, Group F, Member 3Spondylitis, AnkylosingSTAT3 Transcription FactorTh17 CellsAdultFemaleHumansInterleukin-21Interleukin-22InterleukinsEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHistonesInterleukin-17Interleukin-21Interleukin-22InterleukinsJAK2 protein, humanJanus Kinase 2Jumonji Domain-Containing Histone DemethylasesKDM6B protein, humanNuclear Receptor Subfamily 1, Group F, Member 3RORC protein, humanSTAT3 protein, humanSTAT3 Transcription FactorAnkylosing spondylitisEpigenetic regulationH3K27me3Th17 cell differentiation

Identifiers

PMID38948276
PMCPMC11211769

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