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Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine
Here we describe a collaboration between industry, the National Health Service (NHS) and academia that sought to demonstrate how early understanding of both pharmacology and genomics can improve strategies for the development of precision medicines. Diseased tissue ethically acquired from patients s...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924641/ https://www.ncbi.nlm.nih.gov/pubmed/31860681 http://dx.doi.org/10.1371/journal.pone.0226564 |
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author | Cowan, Karen Macluskie, Graeme Finch, Michael Palmer, Colin N. A. Hair, Jane Bylesjo, Max Lynagh, Sarah Brankin, Pamela McNeil, Marian Low, Carolyn Mallinson, David Gourlay, Elaine M. Child, Hannah Cheyne, Linda Bunton, David C. |
author_facet | Cowan, Karen Macluskie, Graeme Finch, Michael Palmer, Colin N. A. Hair, Jane Bylesjo, Max Lynagh, Sarah Brankin, Pamela McNeil, Marian Low, Carolyn Mallinson, David Gourlay, Elaine M. Child, Hannah Cheyne, Linda Bunton, David C. |
author_sort | Cowan, Karen |
collection | PubMed |
description | Here we describe a collaboration between industry, the National Health Service (NHS) and academia that sought to demonstrate how early understanding of both pharmacology and genomics can improve strategies for the development of precision medicines. Diseased tissue ethically acquired from patients suffering from chronic obstructive pulmonary disease (COPD), was used to investigate inter-patient variability in drug efficacy using ex vivo organocultures of fresh lung tissue as the test system. The reduction in inflammatory cytokines in the presence of various test drugs was used as the measure of drug efficacy and the individual patient responses were then matched against genotype and microRNA profiles in an attempt to identify unique predictors of drug responsiveness. Our findings suggest that genetic variation in CYP2E1 and SMAD3 genes may partly explain the observed variation in drug response. |
format | Online Article Text |
id | pubmed-6924641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69246412020-01-07 Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine Cowan, Karen Macluskie, Graeme Finch, Michael Palmer, Colin N. A. Hair, Jane Bylesjo, Max Lynagh, Sarah Brankin, Pamela McNeil, Marian Low, Carolyn Mallinson, David Gourlay, Elaine M. Child, Hannah Cheyne, Linda Bunton, David C. PLoS One Research Article Here we describe a collaboration between industry, the National Health Service (NHS) and academia that sought to demonstrate how early understanding of both pharmacology and genomics can improve strategies for the development of precision medicines. Diseased tissue ethically acquired from patients suffering from chronic obstructive pulmonary disease (COPD), was used to investigate inter-patient variability in drug efficacy using ex vivo organocultures of fresh lung tissue as the test system. The reduction in inflammatory cytokines in the presence of various test drugs was used as the measure of drug efficacy and the individual patient responses were then matched against genotype and microRNA profiles in an attempt to identify unique predictors of drug responsiveness. Our findings suggest that genetic variation in CYP2E1 and SMAD3 genes may partly explain the observed variation in drug response. Public Library of Science 2019-12-20 /pmc/articles/PMC6924641/ /pubmed/31860681 http://dx.doi.org/10.1371/journal.pone.0226564 Text en © 2019 Cowan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Cowan, Karen Macluskie, Graeme Finch, Michael Palmer, Colin N. A. Hair, Jane Bylesjo, Max Lynagh, Sarah Brankin, Pamela McNeil, Marian Low, Carolyn Mallinson, David Gourlay, Elaine M. Child, Hannah Cheyne, Linda Bunton, David C. Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine |
title | Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine |
title_full | Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine |
title_fullStr | Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine |
title_full_unstemmed | Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine |
title_short | Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine |
title_sort | application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924641/ https://www.ncbi.nlm.nih.gov/pubmed/31860681 http://dx.doi.org/10.1371/journal.pone.0226564 |
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