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Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma
BACKGROUND: : With the increasing incidence of asthma, more attention is focused on the diverse and complex nutritional and environmental triggers of asthma exacerbations. Currently, there are no established risk assessment tools to evaluate asthma triggering potentials of most of the nutritional an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717055/ https://www.ncbi.nlm.nih.gov/pubmed/31692590 http://dx.doi.org/10.2147/PGPM.S217535 |
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author | Hachim, Mahmood Yaseen Hachim, Ibrahim Yaseen Elemam, Noha M Hamoudi, Rifat A |
author_facet | Hachim, Mahmood Yaseen Hachim, Ibrahim Yaseen Elemam, Noha M Hamoudi, Rifat A |
author_sort | Hachim, Mahmood Yaseen |
collection | PubMed |
description | BACKGROUND: : With the increasing incidence of asthma, more attention is focused on the diverse and complex nutritional and environmental triggers of asthma exacerbations. Currently, there are no established risk assessment tools to evaluate asthma triggering potentials of most of the nutritional and environmental triggers encountered by asthmatic patients. PURPOSE: The objective of this study is to devise a reliable workflow, capable of estimating the toxicogenomic effect of such factors on key player genes in asthma pathogenesis. METHODS: Gene expression extracted from publicly available datasets of asthmatic bronchial epithelium were subjected to a comprehensive analysis of differential gene expression to identify significant genes involved in asthma development and progression. The identified genes were subjected to Gene Set Enrichment Analysis using a total of 31,826 gene sets related to chemical, toxins, and drugs to identify common agents that share similar asthma-related targets genes and signaling pathways. RESULTS: Our analysis identified 225 differentially expressed genes between severe asthmatic and healthy bronchial epithelium. Gene Set Enrichment Analysis of the identified genes showed that they are involved in response to toxic substances and organic cyclic compounds and are targeted by 41 specific diets, plants products, and plants related toxins (eg adenine, arachidonic acid, baicalein, caffeic acid, corilagin, curcumin, ellagic acid, luteolin, microcystin-RR, phytoestrogens, protoporphyrin IX, purpurogallin, rottlerin, and salazinic acid). Moreover, the identified chemicals share interesting inflammation-related pathways like NF-κB. CONCLUSION: Our analysis was able to explain and predict the toxicity in terms of stimulating the differentially expressed genes between severe asthmatic and healthy epithelium. Such an approach can pave the way to generate a cost-effective and reliable source for asthma-specific toxigenic reports thus allowing the asthmatic patients, physicians, and medical researchers to be aware of the potential triggering factors with fatal consequences. |
format | Online Article Text |
id | pubmed-6717055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-67170552019-11-05 Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma Hachim, Mahmood Yaseen Hachim, Ibrahim Yaseen Elemam, Noha M Hamoudi, Rifat A Pharmgenomics Pers Med Original Research BACKGROUND: : With the increasing incidence of asthma, more attention is focused on the diverse and complex nutritional and environmental triggers of asthma exacerbations. Currently, there are no established risk assessment tools to evaluate asthma triggering potentials of most of the nutritional and environmental triggers encountered by asthmatic patients. PURPOSE: The objective of this study is to devise a reliable workflow, capable of estimating the toxicogenomic effect of such factors on key player genes in asthma pathogenesis. METHODS: Gene expression extracted from publicly available datasets of asthmatic bronchial epithelium were subjected to a comprehensive analysis of differential gene expression to identify significant genes involved in asthma development and progression. The identified genes were subjected to Gene Set Enrichment Analysis using a total of 31,826 gene sets related to chemical, toxins, and drugs to identify common agents that share similar asthma-related targets genes and signaling pathways. RESULTS: Our analysis identified 225 differentially expressed genes between severe asthmatic and healthy bronchial epithelium. Gene Set Enrichment Analysis of the identified genes showed that they are involved in response to toxic substances and organic cyclic compounds and are targeted by 41 specific diets, plants products, and plants related toxins (eg adenine, arachidonic acid, baicalein, caffeic acid, corilagin, curcumin, ellagic acid, luteolin, microcystin-RR, phytoestrogens, protoporphyrin IX, purpurogallin, rottlerin, and salazinic acid). Moreover, the identified chemicals share interesting inflammation-related pathways like NF-κB. CONCLUSION: Our analysis was able to explain and predict the toxicity in terms of stimulating the differentially expressed genes between severe asthmatic and healthy epithelium. Such an approach can pave the way to generate a cost-effective and reliable source for asthma-specific toxigenic reports thus allowing the asthmatic patients, physicians, and medical researchers to be aware of the potential triggering factors with fatal consequences. Dove 2019-08-26 /pmc/articles/PMC6717055/ /pubmed/31692590 http://dx.doi.org/10.2147/PGPM.S217535 Text en © 2019 Hachim et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Hachim, Mahmood Yaseen Hachim, Ibrahim Yaseen Elemam, Noha M Hamoudi, Rifat A Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma |
title | Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma |
title_full | Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma |
title_fullStr | Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma |
title_full_unstemmed | Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma |
title_short | Toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma |
title_sort | toxicogenomic analysis of publicly available transcriptomic data can predict food, drugs, and chemical-induced asthma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717055/ https://www.ncbi.nlm.nih.gov/pubmed/31692590 http://dx.doi.org/10.2147/PGPM.S217535 |
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