Aberrant DNA Methylation: Implications in Racial Health Disparity.

Incidence and mortality rates of colorectal carcinoma (CRC) are higher in African Americans (AAs) than in Caucasian Americans (CAs). Deficient micronutrient intake due to dietary restrictions in racial/ethnic populations can alter genetic and molecular profiles leading to dysregulated methylation pa...

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Main Authors: Xuefeng Wang, Ping Ji, Yuanhao Zhang, Joseph F LaComb, Xinyu Tian, Ellen Li, Jennie L Williams
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4844165?pdf=render
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author Xuefeng Wang
Ping Ji
Yuanhao Zhang
Joseph F LaComb
Xinyu Tian
Ellen Li
Jennie L Williams
author_facet Xuefeng Wang
Ping Ji
Yuanhao Zhang
Joseph F LaComb
Xinyu Tian
Ellen Li
Jennie L Williams
author_sort Xuefeng Wang
collection DOAJ
description Incidence and mortality rates of colorectal carcinoma (CRC) are higher in African Americans (AAs) than in Caucasian Americans (CAs). Deficient micronutrient intake due to dietary restrictions in racial/ethnic populations can alter genetic and molecular profiles leading to dysregulated methylation patterns and the inheritance of somatic to germline mutations.Total DNA and RNA samples of paired tumor and adjacent normal colon tissues were prepared from AA and CA CRC specimens. Reduced Representation Bisulfite Sequencing (RRBS) and RNA sequencing were employed to evaluate total genome methylation of 5'-regulatory regions and dysregulation of gene expression, respectively. Robust analysis was conducted using a trimming-and-retrieving scheme for RRBS library mapping in conjunction with the BStool toolkit.DNA from the tumor of AA CRC patients, compared to adjacent normal tissues, contained 1,588 hypermethylated and 100 hypomethylated differentially methylated regions (DMRs). Whereas, 109 hypermethylated and 4 hypomethylated DMRs were observed in DNA from the tumor of CA CRC patients; representing a 14.6-fold and 25-fold change, respectively. Specifically; CHL1, 4 anti-inflammatory genes (i.e., NELL1, GDF1, ARHGEF4, and ITGA4), and 7 miRNAs (of which miR-9-3p and miR-124-3p have been implicated in CRC) were hypermethylated in DNA samples from AA patients with CRC. From the same sample set, RNAseq analysis revealed 108 downregulated genes (including 14 ribosomal proteins) and 34 upregulated genes (including POLR2B and CYP1B1 [targets of miR-124-3p]) in AA patients with CRC versus CA patients.DNA methylation profile and/or products of its downstream targets could serve as biomarker(s) addressing racial health disparity.
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spelling doaj.art-14cdba6a40924102b3b1d9e27f2a81d92022-12-21T19:28:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01114e015312510.1371/journal.pone.0153125Aberrant DNA Methylation: Implications in Racial Health Disparity.Xuefeng WangPing JiYuanhao ZhangJoseph F LaCombXinyu TianEllen LiJennie L WilliamsIncidence and mortality rates of colorectal carcinoma (CRC) are higher in African Americans (AAs) than in Caucasian Americans (CAs). Deficient micronutrient intake due to dietary restrictions in racial/ethnic populations can alter genetic and molecular profiles leading to dysregulated methylation patterns and the inheritance of somatic to germline mutations.Total DNA and RNA samples of paired tumor and adjacent normal colon tissues were prepared from AA and CA CRC specimens. Reduced Representation Bisulfite Sequencing (RRBS) and RNA sequencing were employed to evaluate total genome methylation of 5'-regulatory regions and dysregulation of gene expression, respectively. Robust analysis was conducted using a trimming-and-retrieving scheme for RRBS library mapping in conjunction with the BStool toolkit.DNA from the tumor of AA CRC patients, compared to adjacent normal tissues, contained 1,588 hypermethylated and 100 hypomethylated differentially methylated regions (DMRs). Whereas, 109 hypermethylated and 4 hypomethylated DMRs were observed in DNA from the tumor of CA CRC patients; representing a 14.6-fold and 25-fold change, respectively. Specifically; CHL1, 4 anti-inflammatory genes (i.e., NELL1, GDF1, ARHGEF4, and ITGA4), and 7 miRNAs (of which miR-9-3p and miR-124-3p have been implicated in CRC) were hypermethylated in DNA samples from AA patients with CRC. From the same sample set, RNAseq analysis revealed 108 downregulated genes (including 14 ribosomal proteins) and 34 upregulated genes (including POLR2B and CYP1B1 [targets of miR-124-3p]) in AA patients with CRC versus CA patients.DNA methylation profile and/or products of its downstream targets could serve as biomarker(s) addressing racial health disparity.http://europepmc.org/articles/PMC4844165?pdf=render
spellingShingle Xuefeng Wang
Ping Ji
Yuanhao Zhang
Joseph F LaComb
Xinyu Tian
Ellen Li
Jennie L Williams
Aberrant DNA Methylation: Implications in Racial Health Disparity.
PLoS ONE
title Aberrant DNA Methylation: Implications in Racial Health Disparity.
title_full Aberrant DNA Methylation: Implications in Racial Health Disparity.
title_fullStr Aberrant DNA Methylation: Implications in Racial Health Disparity.
title_full_unstemmed Aberrant DNA Methylation: Implications in Racial Health Disparity.
title_short Aberrant DNA Methylation: Implications in Racial Health Disparity.
title_sort aberrant dna methylation implications in racial health disparity
url http://europepmc.org/articles/PMC4844165?pdf=render
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