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Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial

Regular aspirin use reduces colon adenoma and carcinoma incidence. UDP-glucuronosyltransferases (UGT) are involved in aspirin metabolism and clearance, and variant alleles in UGT1A6 have been shown to alter salicylic acid metabolism and risk of colon neoplasia. In a randomized, cross-over, placebo-c...

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Autores principales: Thomas, Sushma S., Makar, Karen W., Li, Lin, Zheng, Yingye, Yang, Peiying, Levy, Lisa, Rudolph, Rebecca Y., Lampe, Paul D., Yan, Min, Markowitz, Sanford D., Bigler, Jeannette, Lampe, Johanna W., Potter, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664722/
https://www.ncbi.nlm.nih.gov/pubmed/26697360
http://dx.doi.org/10.1016/j.gdata.2015.08.029
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author Thomas, Sushma S.
Makar, Karen W.
Li, Lin
Zheng, Yingye
Yang, Peiying
Levy, Lisa
Rudolph, Rebecca Y.
Lampe, Paul D.
Yan, Min
Markowitz, Sanford D.
Bigler, Jeannette
Lampe, Johanna W.
Potter, John D.
author_facet Thomas, Sushma S.
Makar, Karen W.
Li, Lin
Zheng, Yingye
Yang, Peiying
Levy, Lisa
Rudolph, Rebecca Y.
Lampe, Paul D.
Yan, Min
Markowitz, Sanford D.
Bigler, Jeannette
Lampe, Johanna W.
Potter, John D.
author_sort Thomas, Sushma S.
collection PubMed
description Regular aspirin use reduces colon adenoma and carcinoma incidence. UDP-glucuronosyltransferases (UGT) are involved in aspirin metabolism and clearance, and variant alleles in UGT1A6 have been shown to alter salicylic acid metabolism and risk of colon neoplasia. In a randomized, cross-over, placebo-controlled trial of 44 healthy men and women, homozygous for UGT1A6*1 or UGT1A6*2, we explored differences between global epithelial and stromal expression, using Affymetrix U133 + 2.0 microarrays and tested effects of 60-day aspirin supplementation (325 mg/d) on epithelial and stromal gene expression and colon prostaglandin E2 (PGE2) levels. We conducted a comprehensive study of differential gene expression between normal human colonic epithelium and stroma from healthy individuals. Although no statistically significant differences in gene expression were observed in response to aspirin or UGT1A6 genotype, we have identified the genes uniquely and reproducibly expressed in each tissue type and have analyzed the biologic processes they represent. Here we describe in detail how the data, deposited in the Gene Expression Omnibus (GEO) – accession number GSE71571 – was generated including the basic analysis as contained in the manuscript published in BMC Medical Genetics with the PMID 25927723 (Thomas et al., 2015 [9]).
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spelling pubmed-46647222015-12-22 Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial Thomas, Sushma S. Makar, Karen W. Li, Lin Zheng, Yingye Yang, Peiying Levy, Lisa Rudolph, Rebecca Y. Lampe, Paul D. Yan, Min Markowitz, Sanford D. Bigler, Jeannette Lampe, Johanna W. Potter, John D. Genom Data Data in Brief Regular aspirin use reduces colon adenoma and carcinoma incidence. UDP-glucuronosyltransferases (UGT) are involved in aspirin metabolism and clearance, and variant alleles in UGT1A6 have been shown to alter salicylic acid metabolism and risk of colon neoplasia. In a randomized, cross-over, placebo-controlled trial of 44 healthy men and women, homozygous for UGT1A6*1 or UGT1A6*2, we explored differences between global epithelial and stromal expression, using Affymetrix U133 + 2.0 microarrays and tested effects of 60-day aspirin supplementation (325 mg/d) on epithelial and stromal gene expression and colon prostaglandin E2 (PGE2) levels. We conducted a comprehensive study of differential gene expression between normal human colonic epithelium and stroma from healthy individuals. Although no statistically significant differences in gene expression were observed in response to aspirin or UGT1A6 genotype, we have identified the genes uniquely and reproducibly expressed in each tissue type and have analyzed the biologic processes they represent. Here we describe in detail how the data, deposited in the Gene Expression Omnibus (GEO) – accession number GSE71571 – was generated including the basic analysis as contained in the manuscript published in BMC Medical Genetics with the PMID 25927723 (Thomas et al., 2015 [9]). Elsevier 2015-09-01 /pmc/articles/PMC4664722/ /pubmed/26697360 http://dx.doi.org/10.1016/j.gdata.2015.08.029 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data in Brief
Thomas, Sushma S.
Makar, Karen W.
Li, Lin
Zheng, Yingye
Yang, Peiying
Levy, Lisa
Rudolph, Rebecca Y.
Lampe, Paul D.
Yan, Min
Markowitz, Sanford D.
Bigler, Jeannette
Lampe, Johanna W.
Potter, John D.
Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial
title Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial
title_full Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial
title_fullStr Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial
title_full_unstemmed Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial
title_short Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial
title_sort tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial
topic Data in Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664722/
https://www.ncbi.nlm.nih.gov/pubmed/26697360
http://dx.doi.org/10.1016/j.gdata.2015.08.029
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