Evidence map›Paper›PMID 42148152›Full record

ReviewFrontiers in molecular biosciences2026

Chemerin/ChemerinR1 axis and inflammation-related diseases.

Jun Li, Changhao Mao, Ke Li, Yan Huang, Yuhan Yang, Kunyi Li, Shuang Li, Lan Wen

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jun Li *School of Clinical Medicine, Chengdu Medical College, Chengdu, China.
Changhao Mao *School of Clinical Medicine, Chengdu Medical College, Chengdu, China.
Ke Li *School of Clinical Medicine, Chengdu Medical College, Chengdu, China.
Yan HuangSchool of Clinical Medicine, Chengdu Medical College, Chengdu, China.
Yuhan YangSchool of Clinical Medicine, Chengdu Medical College, Chengdu, China.
Kunyi LiSchool of Clinical Medicine, Chengdu Medical College, Chengdu, China.
Shuang LiSchool of Clinical Medicine, Chengdu Medical College, Chengdu, China.
Lan WenSchool of Clinical Medicine, Chengdu Medical College, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation-related diseases, including cardiovascular diseases, immune disorders, and infectious diseases, have high prevalence and disability rates, imposing heavy socioeconomic and healthcare burdens. Thus, elucidating the molecular mechanisms underlying inflammation and identifying therapeutic targets are critical for the treatment of inflammation-related diseases. Chemerin, an adipokine and chemotactic protein, primarily mediates its biological effects through ChemerinR1, a G protein-coupled receptor (GPCR). Over the past 3 decades, the Chemerin/ChemerinR1 axis has been implicated in the regulation of various physiological processes, such as inflammation, metabolism, and immune response. We have comprehensively reviewed this axis plays an important role in the onset, progression, and prognosis of inflammation-related diseases, highlighting its translational potential for understanding these diseases and developing targeted therapies. This review aims to elucidate the specific mechanism of the Chemerin/ChemerinR1 axis in inflammation-related diseases. Specifically, the Chemerin/ChemerinR1 axis activates the mitogen-activated protein kinase (MAPK), PI3K/Akt, and NF-κB signaling pathways, thereby further regulating cell functions and the initiation and progression of inflammation. We also elucidate the effect of the Chemerin/ChemerinR1 axis on various inflammation-related diseases, such as hypertension, atherosclerosis, stroke, obesity, rheumatoid arthritis, and inflammatory bowel disease. Additionally, the Chemerin/ChemerinR1 axis can serve as a biomarker for various inflammation-related diseases, enabling early diagnosis, disease monitoring, and evaluation of treatment effects. Therefore, targeting the Chemerin/ChemerinR1 axis holds great potential for the treatment of vascular inflammatory diseases.

Indexed as

cardiovascular diseasescerebrovascular diseasesChemerin/ChemerinR1 axisChemerin peptidesG protein-coupled receptorimmunological diseaseinflammation-related diseasesmetabolic diseases

Identifiers

PMID42148152
PMCPMC13171387

What Socratic holds

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LicenceCC BY
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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.