Evidence map›Paper›PMID 41624379›Full record

ArticleMediators of inflammation2026

Convergent Multistage Evidence Implicates the CCR2-Artemin Immune-Inflammation Axis in Acute Myeloid Leukemia.

Yi Jin, Hui-Min Lu, Xing-Hao Yu, Ming-Zhu Su, Jun Li, Xiao-Min Li, Jian-Hua Jin, Li-Ting Zhang, Yue Wang

Abstract read
In one paragraph

Article in Mediators of inflammation, 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. Gut-reproduction axis: genome-wide pleiotropic and prospective evidence linking inflammatory bowel disease with gynecological disorders.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    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

9 authors.

Yi JinWujin Hospital Affiliated with Jiangsu University, Changzhou, 213017, Jiangsu, China, ujs.edu.cn.ORCID https://orcid.org/0009-0004-8391-3178
Hui-Min LuDepartment of Outpatient and Emergency, The First Affiliated Hospital of Soochow University, Suzhou, 215123, Jiangsu, China, sdfyy.cn.ORCID https://orcid.org/0000-0003-4865-1825
Xing-Hao YuNational Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, 215123, Jiangsu, China, sdfyy.cn.ORCID https://orcid.org/0000-0002-0589-0386
Ming-Zhu SuWujin Hospital Affiliated with Jiangsu University, Changzhou, 213017, Jiangsu, China, ujs.edu.cn.
Jun LiWujin Hospital Affiliated with Jiangsu University, Changzhou, 213017, Jiangsu, China, ujs.edu.cn.
Xiao-Min LiWujin Hospital Affiliated with Jiangsu University, Changzhou, 213017, Jiangsu, China, ujs.edu.cn.
Jian-Hua JinWujin Hospital Affiliated with Jiangsu University, Changzhou, 213017, Jiangsu, China, ujs.edu.cn.ORCID https://orcid.org/0000-0001-8051-6338
Li-Ting ZhangWujin Hospital Affiliated with Jiangsu University, Changzhou, 213017, Jiangsu, China, ujs.edu.cn.ORCID https://orcid.org/0009-0006-0330-9283
Yue WangWujin Hospital Affiliated with Jiangsu University, Changzhou, 213017, Jiangsu, China, ujs.edu.cn.ORCID https://orcid.org/0000-0002-5491-0582

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The immune system and inflammatory proteins influence hematologic malignancies, but causal links with immune cell phenotypes are unclear. Methods: We applied a prespecified, multistage workflow: two-sample and multivariable Mendelian randomization (MVMR; 731 immune traits across 12 hematologic cancers), two-step mediation Mendelian randomization (MR) of 91 circulating inflammatory proteins, MAGMA/FUMA gene and pathway enrichment, and external validation with trait-specific genetic risk scores (GRSs) in UK Biobank (UKB). We then performed Results: Eight immune phenotypes showed FDR-significant causal associations with malignancy, seven of which remained independent in MVMR. In acute myeloid leukemia (AML), Conclusion: This integrative analysis identified

Indexed as

InflammationLeukemia, Myeloid, AcuteReceptors, CCR2HumansProteomicsTHP-1 CellsCCR2 protein, humanReceptors, CCR2acute myeloid leukemiaARTNCCR2genetic risk scoreimmune cellsmediation analysisMendelian randomization

Identifiers

PMID41624379
PMCPMC12860421

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.