Sputum exosomes: promising biomarkers for idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF is complex, we aimed to characterise microRNA (miRNA) content of exosomes from sputum of patients with IPF. Using miRNA quantitative PCR arr...

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Published inThorax Vol. 74; no. 3; pp. 309 - 312
Main Authors Njock, Makon-Sébastien, Guiot, Julien, Henket, Monique A, Nivelles, Olivier, Thiry, Marc, Dequiedt, Franck, Corhay, Jean-Louis, Louis, Renaud E, Struman, Ingrid
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Published England BMJ Publishing Group Ltd and British Thoracic Society 01.03.2019
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Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF is complex, we aimed to characterise microRNA (miRNA) content of exosomes from sputum of patients with IPF. Using miRNA quantitative PCR array, we found a substantial dysregulation of sputum exosomal miRNA levels between patients with IPF and healthy subjects and identified a unique signature of three miRNAs. Interestingly, we found a negative correlation between miR-142-3p and diffusing capacity of the lungs for carbon monoxide/alveolar volume. This is the first characterisation of miRNA content of sputum-derived exosomes in IPF that identified promising biomarkers for diagnosis and disease severity.
AbstractList Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF is complex, we aimed to characterise microRNA (miRNA) content of exosomes from sputum of patients with IPF. Using miRNA quantitative PCR array, we found a substantial dysregulation of sputum exosomal miRNA levels between patients with IPF and healthy subjects and identified a unique signature of three miRNAs. Interestingly, we found a negative correlation between miR-142-3p and diffusing capacity of the lungs for carbon monoxide/alveolar volume. This is the first characterisation of miRNA content of sputum-derived exosomes in IPF that identified promising biomarkers for diagnosis and disease severity.
Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF is complex, we aimed to characterise microRNA (miRNA) content of exosomes from sputum of patients with IPF. Using miRNA quantitative PCR array, we found a substantial dysregulation of sputum exosomal miRNA levels between patients with IPF and healthy subjects and identified a unique signature of three miRNAs. Interestingly, we found a negative correlation between miR-142-3p and diffusing capacity of the lungs for carbon monoxide/alveolar volume. This is the first characterisation of miRNA content of sputum-derived exosomes in IPF that identified promising biomarkers for diagnosis and disease severity.Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF is complex, we aimed to characterise microRNA (miRNA) content of exosomes from sputum of patients with IPF. Using miRNA quantitative PCR array, we found a substantial dysregulation of sputum exosomal miRNA levels between patients with IPF and healthy subjects and identified a unique signature of three miRNAs. Interestingly, we found a negative correlation between miR-142-3p and diffusing capacity of the lungs for carbon monoxide/alveolar volume. This is the first characterisation of miRNA content of sputum-derived exosomes in IPF that identified promising biomarkers for diagnosis and disease severity.
Author Guiot, Julien
Dequiedt, Franck
Thiry, Marc
Henket, Monique A
Louis, Renaud E
Struman, Ingrid
Njock, Makon-Sébastien
Nivelles, Olivier
Corhay, Jean-Louis
AuthorAffiliation 3 Laboratory of Pneumology, GIGA-I3 , University of Liège , Liège , Belgium
2 Pneumology Department , CHU Liège , Liège , Belgium
1 Laboratory of Molecular Angiogenesis, GIGA-R , University of Liège , Liège , Belgium
4 Laboratoire de Biologie Cellulaire et Tissulaire, GIGA-R , University of Liège , Liège , Belgium
5 Laboratoire de Signalisation et Interactions des Protéines, GIGA-R , University of Liège , Liège , Belgium
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/30244194$$D View this record in MEDLINE/PubMed
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Issue 3
Keywords interstitial fibrosis
idiopathic pulmonary fibrosis
Language English
License This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
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Snippet Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF...
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SubjectTerms Age
Ambulatory care
Biochemistry, biophysics & molecular biology
Biochimie, biophysique & biologie moléculaire
Biomarkers
Biomarkers - metabolism
Brief Communication
Case-Control Studies
Cytochrome
Disease
Exosomes - metabolism
Experiments
Female
Gene expression
Humans
idiopathic pulmonary fibrosis
Idiopathic Pulmonary Fibrosis - diagnosis
Idiopathic Pulmonary Fibrosis - etiology
Idiopathic Pulmonary Fibrosis - metabolism
interstitial fibrosis
Life sciences
Male
MicroRNAs
MicroRNAs - metabolism
Patients
Principal components analysis
Pulmonary fibrosis
Sciences du vivant
Sensitivity and Specificity
Sputum - metabolism
Studies
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Title Sputum exosomes: promising biomarkers for idiopathic pulmonary fibrosis
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