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Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids

In this study we aimed to explore the potential biological effect of ethanol exposure on healthy colon epithelial cells using normal human colon 3D organoid “mini-gut” cultures. In numerous published studies ethanol use has been shown to be an environmental risk factor for colorectal cancer (CRC) de...

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Autores principales: Devall, Matthew, Jennelle, Lucas T., Bryant, Jennifer, Bien, Stephanie, Peters, Ulrike, Powell, Steven, Casey, Graham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968849/
https://www.ncbi.nlm.nih.gov/pubmed/31951625
http://dx.doi.org/10.1371/journal.pone.0227116
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author Devall, Matthew
Jennelle, Lucas T.
Bryant, Jennifer
Bien, Stephanie
Peters, Ulrike
Powell, Steven
Casey, Graham
author_facet Devall, Matthew
Jennelle, Lucas T.
Bryant, Jennifer
Bien, Stephanie
Peters, Ulrike
Powell, Steven
Casey, Graham
author_sort Devall, Matthew
collection PubMed
description In this study we aimed to explore the potential biological effect of ethanol exposure on healthy colon epithelial cells using normal human colon 3D organoid “mini-gut” cultures. In numerous published studies ethanol use has been shown to be an environmental risk factor for colorectal cancer (CRC) development; however, the influence of ethanol exposure on normal colon epithelial cell biology remains poorly understood. We investigated the potential molecular effects of ethanol exposure in normal colon 3D organoids in a small pilot study (n = 3) using RNA-seq and ATAC-seq. We identify 1965 differentially expressed genes and 2217 differentially accessible regions of chromatin in response to ethanol treatment. Further, by cross-referencing our results with previously published analysis in colorectal cancer cell lines, we have not only validated a number of reported differentially expressed genes, but also identified several novel candidates for future investigation. In summary, our data highlights the potential importance for the use of normal colon 3D organoid models as a novel tool for the investigation of the relationship between the effects of environmental risk factors associated with colorectal cancer and the molecular mechanisms through which they confer this risk.
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spelling pubmed-69688492020-01-26 Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids Devall, Matthew Jennelle, Lucas T. Bryant, Jennifer Bien, Stephanie Peters, Ulrike Powell, Steven Casey, Graham PLoS One Research Article In this study we aimed to explore the potential biological effect of ethanol exposure on healthy colon epithelial cells using normal human colon 3D organoid “mini-gut” cultures. In numerous published studies ethanol use has been shown to be an environmental risk factor for colorectal cancer (CRC) development; however, the influence of ethanol exposure on normal colon epithelial cell biology remains poorly understood. We investigated the potential molecular effects of ethanol exposure in normal colon 3D organoids in a small pilot study (n = 3) using RNA-seq and ATAC-seq. We identify 1965 differentially expressed genes and 2217 differentially accessible regions of chromatin in response to ethanol treatment. Further, by cross-referencing our results with previously published analysis in colorectal cancer cell lines, we have not only validated a number of reported differentially expressed genes, but also identified several novel candidates for future investigation. In summary, our data highlights the potential importance for the use of normal colon 3D organoid models as a novel tool for the investigation of the relationship between the effects of environmental risk factors associated with colorectal cancer and the molecular mechanisms through which they confer this risk. Public Library of Science 2020-01-17 /pmc/articles/PMC6968849/ /pubmed/31951625 http://dx.doi.org/10.1371/journal.pone.0227116 Text en © 2020 Devall 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
Devall, Matthew
Jennelle, Lucas T.
Bryant, Jennifer
Bien, Stephanie
Peters, Ulrike
Powell, Steven
Casey, Graham
Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids
title Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids
title_full Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids
title_fullStr Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids
title_full_unstemmed Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids
title_short Modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3D colon organoids
title_sort modeling the effect of prolonged ethanol exposure on global gene expression and chromatin accessibility in normal 3d colon organoids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968849/
https://www.ncbi.nlm.nih.gov/pubmed/31951625
http://dx.doi.org/10.1371/journal.pone.0227116
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