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Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples
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, mappin...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969622/ https://www.ncbi.nlm.nih.gov/pubmed/33731770 http://dx.doi.org/10.1038/s41598-021-85345-9 |
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author | Minet, Emmanuel Haswell, Linsey E. Corke, Sarah Banerjee, Anisha Baxter, Andrew Verrastro, Ivan De Abreu e Lima, Francisco Jaunky, Tomasz Santopietro, Simone Breheny, Damien Gaça, Marianna D. |
author_facet | Minet, Emmanuel Haswell, Linsey E. Corke, Sarah Banerjee, Anisha Baxter, Andrew Verrastro, Ivan De Abreu e Lima, Francisco Jaunky, Tomasz Santopietro, Simone Breheny, Damien Gaça, Marianna D. |
author_sort | Minet, Emmanuel |
collection | PubMed |
description | 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 | Online Article Text |
id | pubmed-7969622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79696222021-03-19 Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples Minet, Emmanuel Haswell, Linsey E. Corke, Sarah Banerjee, Anisha Baxter, Andrew Verrastro, Ivan De Abreu e Lima, Francisco Jaunky, Tomasz Santopietro, Simone Breheny, Damien Gaça, Marianna D. Sci Rep Article 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. Nature Publishing Group UK 2021-03-17 /pmc/articles/PMC7969622/ /pubmed/33731770 http://dx.doi.org/10.1038/s41598-021-85345-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Minet, Emmanuel Haswell, Linsey E. Corke, Sarah Banerjee, Anisha Baxter, Andrew Verrastro, Ivan De Abreu e Lima, Francisco Jaunky, Tomasz Santopietro, Simone Breheny, Damien Gaça, Marianna D. Application of text mining to develop AOP-based mucus hypersecretion genesets and confirmation with in vitro and clinical samples |
title | 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_short | 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 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969622/ https://www.ncbi.nlm.nih.gov/pubmed/33731770 http://dx.doi.org/10.1038/s41598-021-85345-9 |
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