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Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment

BACKGROUND: Proteomic studies of respiratory disorders have the potential to identify protein biomarkers for diagnosis and disease monitoring. Utilisation of sensitive quantitative proteomic methods creates opportunities to determine individual patient proteomes. The aim of the current study was to...

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Autores principales: O'Neil, Serena E, Sitkauskiene, Brigita, Babusyte, Agne, Krisiukeniene, Algirda, Stravinskaite-Bieksiene, Kristina, Sakalauskas, Raimundas, Sihlbom, Carina, Ekerljung, Linda, Carlsohn, Elisabet, Lötvall, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206435/
https://www.ncbi.nlm.nih.gov/pubmed/21939520
http://dx.doi.org/10.1186/1465-9921-12-124
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author O'Neil, Serena E
Sitkauskiene, Brigita
Babusyte, Agne
Krisiukeniene, Algirda
Stravinskaite-Bieksiene, Kristina
Sakalauskas, Raimundas
Sihlbom, Carina
Ekerljung, Linda
Carlsohn, Elisabet
Lötvall, Jan
author_facet O'Neil, Serena E
Sitkauskiene, Brigita
Babusyte, Agne
Krisiukeniene, Algirda
Stravinskaite-Bieksiene, Kristina
Sakalauskas, Raimundas
Sihlbom, Carina
Ekerljung, Linda
Carlsohn, Elisabet
Lötvall, Jan
author_sort O'Neil, Serena E
collection PubMed
description BACKGROUND: Proteomic studies of respiratory disorders have the potential to identify protein biomarkers for diagnosis and disease monitoring. Utilisation of sensitive quantitative proteomic methods creates opportunities to determine individual patient proteomes. The aim of the current study was to determine if quantitative proteomics of bronchial biopsies from asthmatics can distinguish relevant biological functions and whether inhaled glucocorticoid treatment affects these functions. METHODS: Endobronchial biopsies were taken from untreated asthmatic patients (n = 12) and healthy controls (n = 3). Asthmatic patients were randomised to double blind treatment with either placebo or budesonide (800 μg daily for 3 months) and new biopsies were obtained. Proteins extracted from the biopsies were digested and analysed using isobaric tags for relative and absolute quantitation combined with a nanoLC-LTQ Orbitrap mass spectrometer. Spectra obtained were used to identify and quantify proteins. Pathways analysis was performed using Ingenuity Pathway Analysis to identify significant biological pathways in asthma and determine how the expression of these pathways was changed by treatment. RESULTS: More than 1800 proteins were identified and quantified in the bronchial biopsies of subjects. The pathway analysis revealed acute phase response signalling, cell-to-cell signalling and tissue development associations with proteins expressed in asthmatics compared to controls. The functions and pathways associated with placebo and budesonide treatment showed distinct differences, including the decreased association with acute phase proteins as a result of budesonide treatment compared to placebo. CONCLUSIONS: Proteomic analysis of bronchial biopsy material can be used to identify and quantify proteins using highly sensitive technologies, without the need for pooling of samples from several patients. Distinct pathophysiological features of asthma can be identified using this approach and the expression of these features is changed by inhaled glucocorticoid treatment. Quantitative proteomics may be applied to identify mechanisms of disease that may assist in the accurate and timely diagnosis of asthma. TRIAL REGISTRATION: ClinicalTrials.gov registration NCT01378039
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spelling pubmed-32064352011-11-03 Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment O'Neil, Serena E Sitkauskiene, Brigita Babusyte, Agne Krisiukeniene, Algirda Stravinskaite-Bieksiene, Kristina Sakalauskas, Raimundas Sihlbom, Carina Ekerljung, Linda Carlsohn, Elisabet Lötvall, Jan Respir Res Research BACKGROUND: Proteomic studies of respiratory disorders have the potential to identify protein biomarkers for diagnosis and disease monitoring. Utilisation of sensitive quantitative proteomic methods creates opportunities to determine individual patient proteomes. The aim of the current study was to determine if quantitative proteomics of bronchial biopsies from asthmatics can distinguish relevant biological functions and whether inhaled glucocorticoid treatment affects these functions. METHODS: Endobronchial biopsies were taken from untreated asthmatic patients (n = 12) and healthy controls (n = 3). Asthmatic patients were randomised to double blind treatment with either placebo or budesonide (800 μg daily for 3 months) and new biopsies were obtained. Proteins extracted from the biopsies were digested and analysed using isobaric tags for relative and absolute quantitation combined with a nanoLC-LTQ Orbitrap mass spectrometer. Spectra obtained were used to identify and quantify proteins. Pathways analysis was performed using Ingenuity Pathway Analysis to identify significant biological pathways in asthma and determine how the expression of these pathways was changed by treatment. RESULTS: More than 1800 proteins were identified and quantified in the bronchial biopsies of subjects. The pathway analysis revealed acute phase response signalling, cell-to-cell signalling and tissue development associations with proteins expressed in asthmatics compared to controls. The functions and pathways associated with placebo and budesonide treatment showed distinct differences, including the decreased association with acute phase proteins as a result of budesonide treatment compared to placebo. CONCLUSIONS: Proteomic analysis of bronchial biopsy material can be used to identify and quantify proteins using highly sensitive technologies, without the need for pooling of samples from several patients. Distinct pathophysiological features of asthma can be identified using this approach and the expression of these features is changed by inhaled glucocorticoid treatment. Quantitative proteomics may be applied to identify mechanisms of disease that may assist in the accurate and timely diagnosis of asthma. TRIAL REGISTRATION: ClinicalTrials.gov registration NCT01378039 BioMed Central 2011 2011-09-22 /pmc/articles/PMC3206435/ /pubmed/21939520 http://dx.doi.org/10.1186/1465-9921-12-124 Text en Copyright ©2011 O'Neil et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
O'Neil, Serena E
Sitkauskiene, Brigita
Babusyte, Agne
Krisiukeniene, Algirda
Stravinskaite-Bieksiene, Kristina
Sakalauskas, Raimundas
Sihlbom, Carina
Ekerljung, Linda
Carlsohn, Elisabet
Lötvall, Jan
Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment
title Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment
title_full Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment
title_fullStr Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment
title_full_unstemmed Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment
title_short Network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment
title_sort network analysis of quantitative proteomics on asthmatic bronchi: effects of inhaled glucocorticoid treatment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206435/
https://www.ncbi.nlm.nih.gov/pubmed/21939520
http://dx.doi.org/10.1186/1465-9921-12-124
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