PBMC gene expression profiles of female Bangladeshi adults chronically exposed to arsenic-contaminated drinking water.
Adult
Arsenic
/ toxicity
Arsenic Poisoning
Bangladesh
Chromosome Aberrations
DNA Methylation
/ drug effects
Drinking Water
/ analysis
Environmental Exposure
/ analysis
Female
Genome-Wide Association Study
Humans
Leukocytes, Mononuclear
/ drug effects
RNA-Seq
Transcriptome
Water Pollutants, Chemical
/ toxicity
Arsenic
Bangladesh
HEALS
PBMC
RNA-Seq
Journal
Environmental pollution (Barking, Essex : 1987)
ISSN: 1873-6424
Titre abrégé: Environ Pollut
Pays: England
ID NLM: 8804476
Informations de publication
Date de publication:
Apr 2020
Apr 2020
Historique:
received:
23
08
2019
revised:
06
11
2019
accepted:
22
11
2019
pubmed:
10
1
2020
medline:
24
6
2020
entrez:
10
1
2020
Statut:
ppublish
Résumé
Arsenic, a class I human carcinogen, is ubiquitously found throughout the environment and around the globe, posing a great public health concern. Notably, Bangladesh and regions of West Bengal have been found to have high levels (0.5-4600 μg/L) of arsenic drinking water contamination, and approximately 50 million of the world's 200 million people chronically exposed to arsenic in Bangladesh alone. This study was carried out to examine genome-wide gene expression changes in individuals chronically exposed to arsenic-contaminated drinking water. Our study population includes twenty-nine Bangladeshi female participants with urinary arsenic levels ranging from 22.32 to 1828.12 μg/g creatinine. RNA extracted from peripheral blood mononuclear cells (PBMCs) were evaluated using RNA-Sequencing analysis. Our results indicate that a total of 1,054 genes were significantly associated with increasing urinary arsenic levels (FDR p < 0.05), which include 418 down-regulated and 636 up-regulated genes. Further Ingenuity Pathway Analysis revealed potential target genes (DAPK1, EGR2, APP), microRNAs (miR-155, -338, -210) and pathways (NOTCH signaling pathway) related to arsenic carcinogenesis. The selection of female-only participants provides a homogenous study population since arsenic has significant sex dependent effects, and the wide exposure range provides new insight for key gene expression changes that correlate with increasing urinary arsenic levels.
Identifiants
pubmed: 31918125
pii: S0269-7491(19)34749-9
doi: 10.1016/j.envpol.2019.113672
pii:
doi:
Substances chimiques
Drinking Water
0
Water Pollutants, Chemical
0
Arsenic
N712M78A8G
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
113672Subventions
Organisme : NIEHS NIH HHS
ID : P42 ES010349
Pays : United States
Organisme : NIEHS NIH HHS
ID : R24 ES028532
Pays : United States
Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare no competing interests.