Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples

Abstract Mucus hypersecretion contributes to lung function impairment observed in COPD (chronic obstructive pulmonary disease), a tobacco smoking-related disease. A detailed mucus hypersecretion adverse outcome pathway (AOP) has been constructed from literature reviews, experimental and clinical dat...

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Autores principales: Emmanuel Minet, Linsey E. Haswell, Sarah Corke, Anisha Banerjee, Andrew Baxter, Ivan Verrastro, Francisco De Abreu e Lima, Tomasz Jaunky, Simone Santopietro, Damien Breheny, Marianna D. Gaça
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/085c7701b32246ae85c6953e73f896e5
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spelling oai:doaj.org-article:085c7701b32246ae85c6953e73f896e52021-12-02T13:17:42ZApplication of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples10.1038/s41598-021-85345-92045-2322https://doaj.org/article/085c7701b32246ae85c6953e73f896e52021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-85345-9https://doaj.org/toc/2045-2322Abstract Mucus hypersecretion contributes to lung function impairment observed in COPD (chronic obstructive pulmonary disease), a tobacco smoking-related disease. A detailed mucus hypersecretion adverse outcome pathway (AOP) has been constructed from literature reviews, experimental and clinical data, mapping key events (KEs) across biological organisational hierarchy leading to an adverse outcome. AOPs can guide the development of biomarkers that are potentially predictive of diseases and support the assessment frameworks of nicotine products including electronic cigarettes. Here, we describe a method employing manual literature curation supported by a focused automated text mining approach to identify genes involved in 5 KEs contributing to decreased lung function observed in tobacco-related COPD. KE genesets were subsequently confirmed by unsupervised clustering against 3 different transcriptomic datasets including (1) in vitro acute cigarette smoke and e-cigarette aerosol exposure, (2) in vitro repeated incubation with IL-13, and (3) lung biopsies from COPD and healthy patients. The 5 KE genesets were demonstrated to be predictive of cigarette smoke exposure and mucus hypersecretion in vitro, and less conclusively predict the COPD status of lung biopsies. In conclusion, using a focused automated text mining and curation approach with experimental and clinical data supports the development of risk assessment strategies utilising AOPs.Emmanuel MinetLinsey E. HaswellSarah CorkeAnisha BanerjeeAndrew BaxterIvan VerrastroFrancisco De Abreu e LimaTomasz JaunkySimone SantopietroDamien BrehenyMarianna D. GaçaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Emmanuel Minet
Linsey E. Haswell
Sarah Corke
Anisha Banerjee
Andrew Baxter
Ivan Verrastro
Francisco De Abreu e Lima
Tomasz Jaunky
Simone Santopietro
Damien Breheny
Marianna D. Gaça
Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
description Abstract Mucus hypersecretion contributes to lung function impairment observed in COPD (chronic obstructive pulmonary disease), a tobacco smoking-related disease. A detailed mucus hypersecretion adverse outcome pathway (AOP) has been constructed from literature reviews, experimental and clinical data, mapping key events (KEs) across biological organisational hierarchy leading to an adverse outcome. AOPs can guide the development of biomarkers that are potentially predictive of diseases and support the assessment frameworks of nicotine products including electronic cigarettes. Here, we describe a method employing manual literature curation supported by a focused automated text mining approach to identify genes involved in 5 KEs contributing to decreased lung function observed in tobacco-related COPD. KE genesets were subsequently confirmed by unsupervised clustering against 3 different transcriptomic datasets including (1) in vitro acute cigarette smoke and e-cigarette aerosol exposure, (2) in vitro repeated incubation with IL-13, and (3) lung biopsies from COPD and healthy patients. The 5 KE genesets were demonstrated to be predictive of cigarette smoke exposure and mucus hypersecretion in vitro, and less conclusively predict the COPD status of lung biopsies. In conclusion, using a focused automated text mining and curation approach with experimental and clinical data supports the development of risk assessment strategies utilising AOPs.
format article
author Emmanuel Minet
Linsey E. Haswell
Sarah Corke
Anisha Banerjee
Andrew Baxter
Ivan Verrastro
Francisco De Abreu e Lima
Tomasz Jaunky
Simone Santopietro
Damien Breheny
Marianna D. Gaça
author_facet Emmanuel Minet
Linsey E. Haswell
Sarah Corke
Anisha Banerjee
Andrew Baxter
Ivan Verrastro
Francisco De Abreu e Lima
Tomasz Jaunky
Simone Santopietro
Damien Breheny
Marianna D. Gaça
author_sort Emmanuel Minet
title Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
title_short Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
title_full Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
title_fullStr Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
title_full_unstemmed Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
title_sort application of text mining to develop aop-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/085c7701b32246ae85c6953e73f896e5
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