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Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects
PURPOSE: Alcohol consumption has been purported to influence many diseases. MicroRNAs (miRNAs) may be influenced by compounds found in alcohol. In this investigation, we test the hypothesis that total alcohol, beer, wine, and hard liquor influence miRNA expression. METHODS: We studied 1447 colorecta...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400787/ https://www.ncbi.nlm.nih.gov/pubmed/28303484 http://dx.doi.org/10.1007/s10552-017-0882-2 |
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author | Mullany, Lila E. Herrick, Jennifer S. Wolff, Roger K. Stevens, John R. Slattery, Martha L. |
author_facet | Mullany, Lila E. Herrick, Jennifer S. Wolff, Roger K. Stevens, John R. Slattery, Martha L. |
author_sort | Mullany, Lila E. |
collection | PubMed |
description | PURPOSE: Alcohol consumption has been purported to influence many diseases. MicroRNAs (miRNAs) may be influenced by compounds found in alcohol. In this investigation, we test the hypothesis that total alcohol, beer, wine, and hard liquor influence miRNA expression. METHODS: We studied 1447 colorectal (CR) cancer cases with normal CR mucosa and carcinoma miRNA expression data along with alcohol consumption data. We analyzed long-term and long-term and current (LTC) alcohol use for beer, liquor, and wine with miRNA expression between paired carcinoma and normal colon and rectal tissues, adjusting for multiple comparisons using the positive false discovery rate q-value. MiRNAs associated significantly with alcohol were examined with all-cause mortality (ACM). MiRNAs associated significantly with ACM were examined with RNA-Seq data. RESULTS: Expression of 84 miRNAs was associated significantly with LTC wine use in normal rectal mucosa. Higher expression of two of these miRNAs significantly worsened ACM: hsa-miR-210 (Hazard Ratio [HR] 1.12, 95% CI (1.03, 1.21), p-value = 0.004), and hsa-miR-92a-1-5p (HR 1.20, 95% CI (1.04, 1.38), p-value = 0.013). These miRNAs were downregulated across levels of LTC wine consumption. CONCLUSIONS: Our results suggest that wine influences miRNA expression in rectal cancer, supporting the hypothesis that components in alcohol influence miRNA expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10552-017-0882-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5400787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-54007872017-05-08 Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects Mullany, Lila E. Herrick, Jennifer S. Wolff, Roger K. Stevens, John R. Slattery, Martha L. Cancer Causes Control Original Paper PURPOSE: Alcohol consumption has been purported to influence many diseases. MicroRNAs (miRNAs) may be influenced by compounds found in alcohol. In this investigation, we test the hypothesis that total alcohol, beer, wine, and hard liquor influence miRNA expression. METHODS: We studied 1447 colorectal (CR) cancer cases with normal CR mucosa and carcinoma miRNA expression data along with alcohol consumption data. We analyzed long-term and long-term and current (LTC) alcohol use for beer, liquor, and wine with miRNA expression between paired carcinoma and normal colon and rectal tissues, adjusting for multiple comparisons using the positive false discovery rate q-value. MiRNAs associated significantly with alcohol were examined with all-cause mortality (ACM). MiRNAs associated significantly with ACM were examined with RNA-Seq data. RESULTS: Expression of 84 miRNAs was associated significantly with LTC wine use in normal rectal mucosa. Higher expression of two of these miRNAs significantly worsened ACM: hsa-miR-210 (Hazard Ratio [HR] 1.12, 95% CI (1.03, 1.21), p-value = 0.004), and hsa-miR-92a-1-5p (HR 1.20, 95% CI (1.04, 1.38), p-value = 0.013). These miRNAs were downregulated across levels of LTC wine consumption. CONCLUSIONS: Our results suggest that wine influences miRNA expression in rectal cancer, supporting the hypothesis that components in alcohol influence miRNA expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10552-017-0882-2) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-03-16 2017 /pmc/articles/PMC5400787/ /pubmed/28303484 http://dx.doi.org/10.1007/s10552-017-0882-2 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Mullany, Lila E. Herrick, Jennifer S. Wolff, Roger K. Stevens, John R. Slattery, Martha L. Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects |
title | Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects |
title_full | Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects |
title_fullStr | Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects |
title_full_unstemmed | Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects |
title_short | Alterations in microRNA expression associated with alcohol consumption in rectal cancer subjects |
title_sort | alterations in microrna expression associated with alcohol consumption in rectal cancer subjects |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400787/ https://www.ncbi.nlm.nih.gov/pubmed/28303484 http://dx.doi.org/10.1007/s10552-017-0882-2 |
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