Publication:
Toxicity screening of air extracts representing different source sectors in the Greater Toronto and Hamilton areas: In vitro oxidative stress, pro-inflammatory response, and toxicogenomic analysis

dc.contributor.authorS. Halappanavaren_US
dc.contributor.authorD. Wuen_US
dc.contributor.authorA. Boyadzhieven_US
dc.contributor.authorA. Solorio-Rodriguezen_US
dc.contributor.authorA. Williamsen_US
dc.contributor.authorN. Jariyasopiten_US
dc.contributor.authorA. Sainien_US
dc.contributor.authorT. Harneren_US
dc.contributor.otherSiriraj Hospitalen_US
dc.contributor.otherHealth Canadaen_US
dc.contributor.otherEnvironment Canadaen_US
dc.date.accessioned2022-08-04T08:03:06Z
dc.date.available2022-08-04T08:03:06Z
dc.date.issued2021-12-01en_US
dc.description.abstractIn the present study, the suitability and sensitivity of different in vitro toxicity endpoints were determined to evaluate and distinguish the specific contributions of polycyclic aromatic carbon (PAC) mixtures from various sites in Toronto (Canada), to pulmonary toxicity. Air samples were collected for two-month periods from April 2014 to March 2015 from one location, and from August 2016 to August 2017 from multiple locations reflecting different geographical areas in Toronto, and the Greater Toronto Area, with varying source emissions including background, traffic, urban, industrial and residential sites. Relative concentrations of PACs and their derivatives in these air samples were characterised. In vitro cytotoxicity, pro-inflammatory, and oxidative stress assays were employed to assess the acute pulmonary effects of urban-air-derived air pollutants. In addition, global transcriptional profiling was utilized to understand how these chemical mixtures exert their harmful effects. Lastly, the transcriptomic data and the chemical profiles for each site and season were used to relate the biological response back to individual constituents. Site-specific responses could not be derived; however, the Spring season was identified as the most responsive through benchmark concentration analysis. A combination of correlational analysis and principal component analysis revealed that nitrated and oxygenated polycyclic aromatic hydrocarbons (PAHs) drive the response at lower concentrations while specific PAHs drive the response at the highest concentration tested. Unsubstituted PAHs are the current targets for analysis as priority pollutants. The present study highlights the importance of by-products of PAH degradation in the assessment of risk. The study also demonstrates the usefulness of in vitro toxicity assays to derive meaningful data in support of risk assessment.en_US
dc.identifier.citationMutation Research - Genetic Toxicology and Environmental Mutagenesis. Vol.872, (2021)en_US
dc.identifier.doi10.1016/j.mrgentox.2021.503415en_US
dc.identifier.issn18793592en_US
dc.identifier.issn13835718en_US
dc.identifier.other2-s2.0-85116676355en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/75915
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85116676355&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectEnvironmental Scienceen_US
dc.titleToxicity screening of air extracts representing different source sectors in the Greater Toronto and Hamilton areas: In vitro oxidative stress, pro-inflammatory response, and toxicogenomic analysisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85116676355&origin=inwarden_US

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