Evidence map›Paper›PMID 41501825›Full record

ArticleRespiratory research2026

Plasma extracellular vesicles-derived MicroRNAs as potential biomarkers in idiopathic pulmonary fibrosis.

Ju Kwang Lee, Jin-Kyung Park, Jae-Yong Nam, Ho Cheol Kim

Abstract read
In one paragraph

Article in Respiratory research, 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

The trial behind it

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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

4 authors.

Ju Kwang Lee *Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.ORCID http://orcid.org/0009-0005-5729-0170
Jin-Kyung Park *Central Research Center, CORESTEMCHEMON Inc., 222-1, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Republic of Korea.
Jae-Yong Nam *Central Research Center, CORESTEMCHEMON Inc., 222-1, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Republic of Korea. wodyd813@gmail.com.
Ho Cheol Kim *Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea. kimhocheol10@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with limited treatment options. Despite antifibrotic therapies, IPF prognosis remains poor, with a variable clinical course. IPF pathogenesis involves recurrent epithelial injury, dysregulated wound healing, and fibroblast activation, leading to excessive extracellular matrix deposition. MicroRNAs (miRNAs) are small regulatory RNAs that modulate gene expression and have been implicated in fibrotic pathways. Encapsulated within plasma-derived extracellular vesicles (EVs), miRNAs are stabilized and transported through the bloodstream, enabling non-invasive access to disease biomarkers for lung pathology.

methodsPlasma samples were obtained from 25 patients with IPF and 8 healthy controls, and the expression of plasma-derived EV miRNAs was analyzed using small RNA sequencing. The functional roles of selected miRNAs were further investigated in human alveolar epithelial cells (A549) and human normal lung fibroblast cells (NHLF) through in vitro experiments.

resultsEV miRNA levels were significantly elevated in patients with IPF. Differential expression analysis revealed upregulation of miR-146b-5p, miR-182-5p, and miR-199a-3p and downregulation of miR-92a-3p in the IPF group. Pathway analysis of predicted target genes indicated enrichment in biological processes relevant to IPF pathogenesis, including epithelial proliferation, wound healing, Wnt signaling, and immune regulation. In vitro experiments further demonstrated that overexpression of plasma-derived EV miRNAs modulated fibrogenic marker expression by either enhancing or suppressing TGF-β signaling, depending on the specific miRNA.

conclusionsThese findings indicate that the identified miRNAs might be involved in fibrotic responses in lung resident cells and may have potential as non-invasive biomarkers, providing preliminary mechanistic insights into the pathogenesis of IPF.

Indexed as

Extracellular VesiclesIdiopathic Pulmonary FibrosisMicroRNAsAgedBiomarkersFemaleHumansMaleMiddle AgedBiomarkersMicroRNAsExtracellular vesiclesIdiopathic pulmonary fibrosisMicroRNAs

Identifiers

PMID41501825
PMCPMC12870188

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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.