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dc.contributor.authorLee, H.S.-
dc.contributor.authorYoon, J.-S.-
dc.contributor.authorSong, M.-
dc.contributor.authorShin, C.-Y.-
dc.contributor.authorChung, H.S.-
dc.contributor.authorRyu, J.-C.-
dc.date.accessioned2024-01-20T13:32:25Z-
dc.date.available2024-01-20T13:32:25Z-
dc.date.created2021-08-31-
dc.date.issued2012-12-
dc.identifier.issn2005-9752-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/128635-
dc.description.abstractLow-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.-
dc.languageEnglish-
dc.publisherKluwer Academic Publishers-
dc.subject3 (4, 5 dimethyl 2 thiazolyl) 2, 5 diphenyltetrazolium bromide-
dc.subjectaldehyde-
dc.subjectbutyraldehyde-
dc.subjectestrogen-
dc.subjectheptanaldehyde-
dc.subjecthexanal-
dc.subjectmessenger RNA-
dc.subjectnonanaldehyde-
dc.subjectoctanal-
dc.subjectpentanaldehyde-
dc.subjectpropionaldehyde-
dc.subjectunclassified drug-
dc.subjectair pollutant-
dc.subjectarticle-
dc.subjectcancer cell-
dc.subjectcancer cell culture-
dc.subjectcell adhesion-
dc.subjectcell hybridization-
dc.subjectcell proliferation-
dc.subjectcell viability-
dc.subjectcontrolled study-
dc.subjectcytotoxicity-
dc.subjectdown regulation-
dc.subjectenvironmental exposure-
dc.subjectgene expression-
dc.subjectgenetic analysis-
dc.subjectgenome analysis-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectimmune response-
dc.subjectin vitro study-
dc.subjectinflammation-
dc.subjectlung alveolus epithelium-
dc.subjectlung cancer-
dc.subjectmicroarray analysis-
dc.subjectnucleotide sequence-
dc.subjectspectrophotometry-
dc.subjectupregulation-
dc.titleGene expression profiling of low dose exposure of saturated aliphatic aldehydes in A549 human alveolar epithelial cells-
dc.typeArticle-
dc.identifier.doi10.1007/s13530-012-0140-7-
dc.description.journalClass1-
dc.identifier.bibliographicCitationToxicology and Environmental Health Sciences, v.4, no.4, pp.211 - 217-
dc.citation.titleToxicology and Environmental Health Sciences-
dc.citation.volume4-
dc.citation.number4-
dc.citation.startPage211-
dc.citation.endPage217-
dc.description.journalRegisteredClassscopus-
dc.identifier.scopusid2-s2.0-84872356063-
dc.type.docTypeArticle-
dc.subject.keywordPlus3 (4, 5 dimethyl 2 thiazolyl) 2, 5 diphenyltetrazolium bromide-
dc.subject.keywordPlusaldehyde-
dc.subject.keywordPlusbutyraldehyde-
dc.subject.keywordPlusestrogen-
dc.subject.keywordPlusheptanaldehyde-
dc.subject.keywordPlushexanal-
dc.subject.keywordPlusmessenger RNA-
dc.subject.keywordPlusnonanaldehyde-
dc.subject.keywordPlusoctanal-
dc.subject.keywordPluspentanaldehyde-
dc.subject.keywordPluspropionaldehyde-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusair pollutant-
dc.subject.keywordPlusarticle-
dc.subject.keywordPluscancer cell-
dc.subject.keywordPluscancer cell culture-
dc.subject.keywordPluscell adhesion-
dc.subject.keywordPluscell hybridization-
dc.subject.keywordPluscell proliferation-
dc.subject.keywordPluscell viability-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPluscytotoxicity-
dc.subject.keywordPlusdown regulation-
dc.subject.keywordPlusenvironmental exposure-
dc.subject.keywordPlusgene expression-
dc.subject.keywordPlusgenetic analysis-
dc.subject.keywordPlusgenome analysis-
dc.subject.keywordPlushuman-
dc.subject.keywordPlushuman cell-
dc.subject.keywordPlusimmune response-
dc.subject.keywordPlusin vitro study-
dc.subject.keywordPlusinflammation-
dc.subject.keywordPluslung alveolus epithelium-
dc.subject.keywordPluslung cancer-
dc.subject.keywordPlusmicroarray analysis-
dc.subject.keywordPlusnucleotide sequence-
dc.subject.keywordPlusspectrophotometry-
dc.subject.keywordPlusupregulation-
dc.subject.keywordAuthorA549-
dc.subject.keywordAuthorAldehydes-
dc.subject.keywordAuthorGene ontology (GO)-
dc.subject.keywordAuthorMicroarray-
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