<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Krivoshiev BV</submitter><funding>FP7 Health</funding><funding>Agentschap voor Innovatie door Wetenschap en Technologie</funding><pagination>492-502</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6060682</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(3)</volume><pubmed_abstract>The flame retardant, 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO), has been receiving great interest given its superior fire protection properties, and its predicted low level of persistence, bioaccumulation, and toxicity. However, empirical toxicological data that are essential for a complete hazard assessment are severely lacking. In this study, we attempted to identify the potential toxicological modes of action by transcriptome (RNA-seq) profiling of the human liver hepatocellular carcinoma cell line, HepG2. Such insight may help in identifying compounds of concern and potential toxicological phenotypes. DOPO was found to have little cytotoxic potential, with lower effective concentrations compared to other flame retardants studied in the same cell line. Differentially exp</pubmed_abstract><journal>Toxicology research</journal><pubmed_title>Transcriptome profiling of HepG2 cells exposed to the flame retardant 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO).</pubmed_title><pmcid>PMC6060682</pmcid><funding_grant_id>264600</funding_grant_id><pubmed_authors>Beemster GTS</pubmed_authors><pubmed_authors>Blust R</pubmed_authors><pubmed_authors>Sprangers K</pubmed_authors><pubmed_authors>Cuypers B</pubmed_authors><pubmed_authors>Krivoshiev BV</pubmed_authors><pubmed_authors>Husson SJ</pubmed_authors><pubmed_authors>Laukens K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome profiling of HepG2 cells exposed to the flame retardant 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO).</name><description>The flame retardant, 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO), has been receiving great interest given its superior fire protection properties, and its predicted low level of persistence, bioaccumulation, and toxicity. However, empirical toxicological data that are essential for a complete hazard assessment are severely lacking. In this study, we attempted to identify the potential toxicological modes of action by transcriptome (RNA-seq) profiling of the human liver hepatocellular carcinoma cell line, HepG2. Such insight may help in identifying compounds of concern and potential toxicological phenotypes. DOPO was found to have little cytotoxic potential, with lower effective concentrations compared to other flame retardants studied in the same cell line. Differentially exp</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 May</publication><modification>2025-04-19T17:55:52.322Z</modification><creation>2019-08-04T07:25:50Z</creation></dates><accession>S-EPMC6060682</accession><cross_references><pubmed>30090599</pubmed><doi>10.1039/c8tx00006a</doi></cross_references></HashMap>