Gene expression profiling of low dose exposure of saturated aliphatic aldehydes in A549 human alveolar epithelial cells

Authors
Lee, H.S.Yoon, J.-S.Song, M.Shin, C.-Y.Chung, H.S.Ryu, J.-C.
Issue Date
2012-12
Publisher
Kluwer Academic Publishers
Citation
Toxicology and Environmental Health Sciences, v.4, no.4, pp.211 - 217
Abstract
Low-molecular weight saturated aliphatic aldehydes (LSAAs), which include propanal, butanal, pentanal, hexanal, octanal, nonanal and heptanal, are volatile organic compounds (VOCs). They are ubiquitous in the environment of our daily life. Although LSAAs are harmful, with mutagenic and carcinogenic effects, the mechanisms underlying the toxicity of volatile aldehydes are still unclear. Therefore, in this study, we performed genome-wide expression profile analysis of A549 human alveolar epithelial cells exposed to seven LSSAs. We selected genes whose expression was changed more than 1.5-fold in A549 cells exposed to LSAAs by analysis of gene expression profiles using human oligonucleotide chips. Through gene expression profiling, we showed that LSSAs are related to the key biological processes defense response, inflammatory response and immune response in gene ontology (GO) analysis. In addition, we identified two genes that were up-regulated (GREB1, BC009808) and four that were down-regulated (UCP1, TCP11, FNDC3A, LOC645206) by all the tested LSAAs. Our data suggest that LSAAs exert toxic effects on A549 cells by modulating mRNA expression. Moreover, we suggest that genes expressed in response to LSAAs represent a molecular signature that can be widely used, in combination with more traditional techniques, to assess and predict the toxicity caused by exposure to LSAAs. ? 2012 Korean Society of Environmental Risk Assessment and Health Science and Springer Science+Business Media Dordrecht.
Keywords
3 (4, 5 dimethyl 2 thiazolyl) 2, 5 diphenyltetrazolium bromide; aldehyde; butyraldehyde; estrogen; heptanaldehyde; hexanal; messenger RNA; nonanaldehyde; octanal; pentanaldehyde; propionaldehyde; unclassified drug; air pollutant; article; cancer cell; cancer cell culture; cell adhesion; cell hybridization; cell proliferation; cell viability; controlled study; cytotoxicity; down regulation; environmental exposure; gene expression; genetic analysis; genome analysis; human; human cell; immune response; in vitro study; inflammation; lung alveolus epithelium; lung cancer; microarray analysis; nucleotide sequence; spectrophotometry; upregulation; 3 (4, 5 dimethyl 2 thiazolyl) 2, 5 diphenyltetrazolium bromide; aldehyde; butyraldehyde; estrogen; heptanaldehyde; hexanal; messenger RNA; nonanaldehyde; octanal; pentanaldehyde; propionaldehyde; unclassified drug; air pollutant; article; cancer cell; cancer cell culture; cell adhesion; cell hybridization; cell proliferation; cell viability; controlled study; cytotoxicity; down regulation; environmental exposure; gene expression; genetic analysis; genome analysis; human; human cell; immune response; in vitro study; inflammation; lung alveolus epithelium; lung cancer; microarray analysis; nucleotide sequence; spectrophotometry; upregulation; A549; Aldehydes; Gene ontology (GO); Microarray
ISSN
2005-9752
URI
https://pubs.kist.re.kr/handle/201004/128635
DOI
10.1007/s13530-012-0140-7
Appears in Collections:
KIST Article > 2012
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