Evidence map›Paper›PMID 42421500›Full record

ReviewEuropean cytokine network2026

Targeting the cytokine-epigenetic axis: a new paradigm and prospects for disease treatment.

Yuyue Luo, Yikan Zheng, Jie Qin, Jinwei Liu, Yuhan Ma, Jingda Li, Jun Li, Wenlong Sun, Qian Zhang, Mengyao Li

Abstract readReview
PubMed Publisher
In one paragraph

Review in European cytokine network, 2026. 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

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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Yuyue Luo *School of Life Sciences and Medicine, Shandong University of Technology, Zibo, China.
Yikan Zheng *First Clinical Medical College, Inner Mongolia Medical University, Hohhot, China.
Jie Qin *School of Life Sciences and Medicine, Shandong University of Technology, Zibo, China.
Jinwei LiuFirst Clinical Medical College, Inner Mongolia Medical University, Hohhot, China.
Yuhan MaFirst Clinical Medical College, Inner Mongolia Medical University, Hohhot, China.
Jingda LiCollege of Life Science, Yangtze University, Jingzhou, China.
Jun LiCollege of Pharmacy, Inner Mongolia Medical University, Hohhot, China.
Wenlong SunSchool of Life Sciences and Medicine, Shandong University of Technology, Zibo, China.
Qian ZhangFirst Clinical Medical College, Inner Mongolia Medical University, Hohhot, China.
Mengyao LiState Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Funding

Natural Science Foundation of Hubei Province 2025AFB923Science and Technology Department of Xizang Autonomous Region XZ202401YD0002C
6 · The paper itself

Abstract

Cytokines, as key signaling molecules, are involved in the regulation of physiological and pathological processes such as inflammation, immunity, and cell growth. Epigenetic mechanisms, including DNA methylation, histone modifications, chromatin remodeling, and non-coding RNAs, enable precise control of gene expression without changing the DNA sequence. Recent studies have revealed that cytokines interact with epigenetic regulation to form a dynamic and complex "cytokine-epigenetic axis". Through metabolic reprogramming and regulation of epigenetic enzyme activity, this axis affects gene expression patterns at both transcriptional and post-transcriptional levels, thereby contributing to the initiation and progression of various diseases, including autoimmune diseases, neurodegenerative diseases, neuropsychiatric disorders, metabolic diseases, and cancer. Targeting this regulatory axis by combining interventions on upstream cytokine signaling and downstream epigenetic enzymes represents a new precision therapeutic strategy for overcoming resistance to monotherapy and achieving disease-modifying treatment. This review describes how cytokines regulate epigenetic modification substrates through metabolic reprogramming and directly regulate epigenetic enzyme activity via JAK-STAT, NF-κB, and TGF-β/Smad pathways; how this axis drives disease chronicity and therapy resistance across autoimmune, neurodegenerative, metabolic, and neoplastic diseases by establishing long-lasting functional reprogramming; and emerging strategies targeting this axis through combined interventions, precision medicine, and disease memory reprogramming.

Indexed as

CytokinesEpigenesis, GeneticAnimalsDNA MethylationHumansMetabolic DiseasesMetabolic ReprogrammingNeoplasmsNeurodegenerative DiseasesSignal TransductionCytokinesCytokinesDNA methylationepigeneticshistone modificationsimmunometabolismtargeted therapy

Identifiers

What Socratic holds

Textmetadata
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.