Evidence map›Paper›PMID 41286919›Full record

ReviewJournal of translational medicine2025

Epigenetic modifier m⁶A methylation: insights into the pathogenesis and therapeutic potential of autoimmune diseases.

Xue Lv, Wenxin Zhang, Yuefang Liu, Yuelin Hu, Xin Wang, Hongsong Yu

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

6 authors.

Xue Lv *Department of Immunology, Special Key Laboratory of Gene Detection and Therapy of Guizhou Province, Zunyi Medical University, No.1 Campus Road, Xinpu District, Zunyi, Guizhou, 563000, China.
Wenxin Zhang *Department of Immunology, Special Key Laboratory of Gene Detection and Therapy of Guizhou Province, Zunyi Medical University, No.1 Campus Road, Xinpu District, Zunyi, Guizhou, 563000, China.
Yuefang Liu *School of Basic Medical Sciences, Special Key Laboratory of Ocular Diseases of Guizhou Province, Zunyi Medical University, Zunyi, Guizhou, China.
Yuelin HuDepartment of Immunology, Special Key Laboratory of Gene Detection and Therapy of Guizhou Province, Zunyi Medical University, No.1 Campus Road, Xinpu District, Zunyi, Guizhou, 563000, China.
Xin WangSchool of Basic Medical Sciences, Special Key Laboratory of Ocular Diseases of Guizhou Province, Zunyi Medical University, Zunyi, Guizhou, China.
Hongsong YuDepartment of Immunology, Special Key Laboratory of Gene Detection and Therapy of Guizhou Province, Zunyi Medical University, No.1 Campus Road, Xinpu District, Zunyi, Guizhou, 563000, China. yuhongsong@163.com.ORCID 0000-0002-1209-2104

Funding

Guizhou Provincial Science and Technology Department gzwkj2025-624, gzwkj2025-092National Natural Science Foundation of China 82160154the Hundred-level Innovative Talent Foundation of Guizhou Province QKH-PTRC-GCC [2023]041the Program for Excellent Young Talents of Zunyi Medical University 18-ZY-001the Program for Science and Technology Joint Fund Project in Zunyi Science and Technology Bureau and Zunyi Medical University ZSKH-HZ-2024-319, QKPTRC-2021-1350-054
6 · The paper itself

Abstract

N6-methyladenosine (m⁶A) methylation is a predominant form of RNA modification in eukaryotic cells. It exerts profound influence over the processing of mRNA, rRNA and tRNA, thereby playing a critical role in various biological processes, including RNA transcription, splicing, degradation, and translation regulation. The m⁶A methylation significantly affects cell fate and signal transduction pathways by regulating gene expression. Notably, aberrant m⁶A modification is strongly associated with the onset and progression of autoimmune diseases. Emerging evidence indicates that these regulatory factors display disease-specific expression patterns and functional roles, influencing immune-cell differentiation and effector functions, inflammatory responses, and tissue injury. This article provides an overview of recent advances in m⁶A biology in autoimmunity and discusses their implications for diagnosis and therapeutic intervention.Clinical trial number Not applicable.

Indexed as

AdenosineAutoimmune DiseasesEpigenesis, GeneticAnimalsEpitranscriptomeHumansMethylationRNA MethylationAdenosineN-methyladenosineAutoimmune diseasesDiagnosisM⁶A methylationRegulationTherapeutic intervention

Identifiers

PMID41286919
PMCPMC12642297

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.