Evidence map›Paper›PMID 36330380›Full record

ArticleMediators of inflammation2022

Comprehensive Analysis and Functional Characteristics of Differential Expression of N6-Methyladenosine Methylation Modification in the Whole Transcriptome of Rheumatoid Arthritis.

Lei Wan, Jian Liu, Chuanbing Huang, Ziheng Zhu, Kun Wang, Guanghan Sun, Lei Zhu, Zhongxiang Hu

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  6. The Signature of Serum Modified Nucleosides in Uveitis.Investigative ophthalmology & visual science · 2025
    Article
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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

8 authors at 3 institutions in 1 country.

Lei WanThe First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230038, China.ORCID https://orcid.org/0000-0001-7855-0422
Jian LiuThe First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230038, China.ORCID https://orcid.org/0000-0001-7352-6757
Chuanbing HuangThe First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230038, China.ORCID https://orcid.org/0000-0002-5832-3094
Ziheng ZhuThe First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230038, China.ORCID https://orcid.org/0000-0001-7317-427X
Kun WangKey Laboratory of Xin'an Medical Education Ministry, Hefei 230038, China.ORCID https://orcid.org/0000-0002-9926-2005
Guanghan SunCollege of Traditional Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.ORCID https://orcid.org/0000-0002-0809-2291
Lei ZhuThe First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230038, China.ORCID https://orcid.org/0000-0002-6082-7291
Zhongxiang HuThe First Affiliated Hospital of University of Science and Technology of China, Hefei 230000, China.ORCID https://orcid.org/0000-0003-0783-3462
Anhui University of Traditional Chinese Medicine · CNMinistry of Education of the People's Republic of China · CNUniversity of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-methyladenosine (m6A) modification is the most prevalent chemical modification in eukaryotic mRNA and is associated with the development of various immune diseases. However, the role of m6A methylation in rheumatoid arthritis (RA) development is unclear. We preliminarily explored the role of m6A methylation-related mRNAs in RA for its clinical application. The discovery of m6A methylation-modifying genes in this study may provide a fresh perspective on the development of drugs for RA treatment. High-throughput sequencing combined with methylated RNA immunoprecipitation (MeRIP-seq) and RNA sequencing were used to assess whole-transcriptome m6A modifications in the synovium of patients with RA. The relationship between m6A-modified target genes and RA inflammation and macrophages was determined. The expression of the m6A-modified significant transcript-enriched inflammatory signaling pathway was assessed through animal experiments. Differentially expressed m6A genes were correlated with macrophage activation involved in immune response, vascular endothelium, MAPK signaling pathway, PI3K - Akt signaling pathway, and other inflammatory processes. Furthermore, combined analysis with m6A-seq and RNA-seq revealed 120 genes with significant changes in both m6A modification and mRNA expression. We selected the top 3 candidate mRNAs that were upregulated and downregulated simultaneously. The expression of phosphatase and tensin homolog deleted on chromosome ten (

Indexed as

Arthritis, RheumatoidTranscriptomeAdenosineAnimalsInflammationMethylationPhosphatidylinositol 3-KinasesRNA, MessengerAdenosinePhosphatidylinositol 3-KinasesRNA, Messenger

Identifiers

PMID36330380
PMCPMC9626244
OpenAlexW4307235764

What OpenQuestion holds

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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.