Evidence map›Paper›PMID 41756236›Full record

ArticleFrontiers in pharmacology2026

LYVE-1 identifies asthma and drives PDGF-BB-induced proliferation, migration, and oxidative stress in airway smooth muscle cells via the PI3K/Akt pathway.

Yunbo Tang, Nan Zhou, Xiaohui Ni

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. 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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yunbo Tang *Department of Respiratory and Critical Care Medicine, Nantong Second People's Hospital, Nantong, Jiangsu, China.
Nan Zhou *Department of Respiratory and Critical Care Medicine, Nantong Second People's Hospital, Nantong, Jiangsu, China.
Xiaohui NiDepartment of Respiratory and Critical Care Medicine, Nantong Second People's Hospital, Nantong, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Asthma is a chronic inflammatory airway disease characterized by airflow limitations, airway remodeling, and immune dysregulation. Lymphatic vessel endothelial hyaluronan receptor-1 (LYVE-1) has recently been implicated in inflammatory and remodeling processes in the body. However, its clinical significance and mechanistic role in asthma are unclear. This study aimed to investigate the association between soluble LYVE-1 (sLYVE-1) levels and asthma severity, airway inflammation, and remodeling, and to elucidate its regulatory role in airway smooth muscle cell (ASMC) activation via the PI3K/Akt signaling pathway. Methods: A total of 238 participants were enrolled, including 80 healthy controls, 72 patients with asthma who were in remission, and 86 patients with acute asthma. Clinical characteristics, pulmonary function parameters, inflammatory and remodeling biomarkers, and serum sLYVE-1 levels were assessed. Correlation analyses were performed to evaluate the relationship between sLYVE-1 and disease-related parameters. Mechanistic studies were conducted Results: Serum sLYVE-1 levels were significantly elevated in patients with asthma and progressively increased with disease severity. sLYVE-1 levels were inversely correlated with forced expiratory volume in one second (FEV1) and FEV1/FVC and positively correlated with total immune globulin E (IgE), eosinophil counts, T-helper cell type 2 (Th2) and T-helper cell type 17 (Th17) cell proportions, fractional exhaled nitric oxide (FeNO), type 2 cytokines, and airway remodeling-associated mediators, including vascular endothelial growth factor A (VEGF-A), stromal-derived factor 1α (SDF-1α), transforming growth factor-β1 (TGF-β1), matrix metalloproteinases-9 (MMP-9), and hyaluronan (all Conclusion: Elevated circulating sLYVE-1 levels are closely associated with asthma severity, airway inflammation, and airway remodeling. Mechanistically, LYVE-1 promoted PDGF-BB-induced ASMC activation through PI3K/Akt signaling, highlighting LYVE-1 as a potential biomarker and potential therapeutic target for asthma.

Indexed as

airway inflammationairway remodelingasthmaPI3K/Akt pathwaysLYVE-1

Identifiers

PMID41756236
PMCPMC12932558

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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.