Evidence map›Paper›PMID 41274972›Full record

ArticleScientific reports2025

hsa_circ_0001818 regulates the function of macrophages in sepsis by inhibiting miR-17-3p, miR-433-3p, and miR-642a-5p.

Chang Tian, Min Zhao, Xijia Zhou, Shan Cong, Ke Wang

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Chang TianDepartment of Respiratory and Critical Care Medicine, The Second Hospital of Jilin University, Changchun, 130041, Jilin, P. R. China.
Min ZhaoDepartment of Respiratory and Critical Care Medicine, Tianjin Chest Hospital, Tianjin, 300010, P. R. China.
Xijia ZhouDepartment of Respiratory and Critical Care Medicine, The Second Hospital of Jilin University, Changchun, 130041, Jilin, P. R. China.
Shan CongDepartment of Respiratory and Critical Care Medicine, The Second Hospital of Jilin University, Changchun, 130041, Jilin, P. R. China.
Ke WangDepartment of Respiratory and Critical Care Medicine, The Second Hospital of Jilin University, Changchun, 130041, Jilin, P. R. China. wke@jlu.edu.cn.

Funding

Disciplinary Crossing and Integration and innovation project of Norman Bethune Health Science Center of Jilin University 2022JBGS07Doctoral Fund Project of Affiliated Hospital of Hebei University 2023BSJJ03President's Scientific Research Fund Project of Hebei University XZJJ202319the Department of Education of Hebei Province QN2024025the Department of Science and Technology of Jilin Province 20240305080YY
6 · The paper itself

Abstract

Sepsis is a leading cause of death due to severe infections. Macrophages are important players in regulating the development of sepsis. Notably, hsa_circ_0001818 is highly expressed in the serum exosomes of sepsis patients and has shown potential as a diagnostic marker for the condition. However, its regulatory role in sepsis remains unclear. Here, we reported that hsa_circ_0001818 expression in macrophages is increased in sepsis. After hsa_circ_0001818 silencing, the apoptotic rate and release of inflammatory cytokines decreased, while phagocytic function of macrophages increased. In contrast, after hsa_circ_0001818 overexpression, the apoptotic rate and the release of inflammatory factors increased, whereas phagocytic function of macrophages decreased. In addition, mechanistic studies and rescue experiments confirmed that hsa_circ_0001818 adsorbs miR-17-3p, miR-433-3p, and miR-642a-5p as sponges, competitively inhibiting the expression of downstream target genes and regulating macrophage function. That is, hsa_circ_0001818 increased the apoptosis rate of macrophages through the miR-17-3p/caspase-3 (CASP3) axis, inhibited the phagocytic function of macrophages by adsorbing miR-433-3p and miR-642a-5p, and increased the secretion level of macrophage inflammatory factors by regulating the zinc finger and BTB domain-containing 20 (ZBTB20)/nuclear factor kappa-B (NF-κB) axis through miR-433-3p and miR-642a-5p. This study revealed the important role of hsa_circ_0001818 in sepsis and provided a new theoretical basis for the precise treatment of sepsis.

Indexed as

MacrophagesMicroRNAsRNA, CircularSepsisAnimalsApoptosisCaspase 3Gene Expression RegulationHumansMaleMicePhagocytosisCaspase 3MicroRNAsRNA, CircularApoptosisHsa_circ_0001818Inflammatory responseMacrophagePhagocytosisSepsis

Identifiers

PMID41274972
PMCPMC12749644

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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.