<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nellis M</submitter><funding>UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES</funding><funding>University of Texas Medical Branch Center for Environmental Toxicology</funding><funding>NCATS NIH HHS</funding><funding>EMORY UNIVERSITY</funding><funding>Brown Foundation</funding><funding>NIEHS NIH HHS</funding><funding>National Institutes of Health</funding><funding>Health Effects Institute</funding><funding>Arkansas Biosciences Institute</funding><pagination>152987</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9062885</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>463</volume><pubmed_abstract>1,3-Butadiene (BD) exposure is known to cause numerous adverse health effects, including cancer, in animals and humans. BD is metabolized to reactive epoxide intermediates, which are genotoxic, but it is not well know what other effects BD has on cellular metabolism. We examined the effects of exposure to BD on the mouse lung metabolome in the genetically heterogeneous collaborative cross outbred mouse model. Mice were exposed to 3 concentra-tions of BD for 10 days (2, 20, and 200 ppm), and lung tissues were analyzed using high-resolution mass spectrometry-based metabolomics. As compared to controls (0 ppm BD), BD had extensive effects on lung metabolism at all concentrations of exposure, including the lowest concentration of 2 ppm, as reflected by reprogramming of multiple metabolic pathw</pubmed_abstract><journal>Toxicology</journal><pubmed_title>Lung metabolome of 1,3-butadiene exposed Collaborative Cross mice reflects metabolic phenotype of human lung cancer.</pubmed_title><pmcid>PMC9062885</pmcid><funding_grant_id>P30ES019776</funding_grant_id><funding_grant_id>UL1TR000039</funding_grant_id><funding_grant_id>R21ES019684</funding_grant_id><funding_grant_id>UL1 TR000039</funding_grant_id><funding_grant_id>T32 ES007254</funding_grant_id><funding_grant_id>P30 ES030285</funding_grant_id><funding_grant_id>R21ES023046</funding_grant_id><funding_grant_id>R21 ES019684</funding_grant_id><funding_grant_id>P30 ES019776</funding_grant_id><funding_grant_id>HEI4907-RFPA09-5/12-1</funding_grant_id><funding_grant_id>R21 ES031824</funding_grant_id><funding_grant_id>R21 ES023046</funding_grant_id><funding_grant_id>R21ES031824</funding_grant_id><funding_grant_id>T32ES007254</funding_grant_id><funding_grant_id>F32 ES013107</funding_grant_id><pubmed_authors>Nellis M</pubmed_authors><pubmed_authors>Liu K</pubmed_authors><pubmed_authors>Caperton CO</pubmed_authors><pubmed_authors>Hallberg LM</pubmed_authors><pubmed_authors>Ameredes BT</pubmed_authors><pubmed_authors>Jones DP</pubmed_authors><pubmed_authors>Go YM</pubmed_authors><pubmed_authors>Boysen G</pubmed_authors><pubmed_authors>Tran V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lung metabolome of 1,3-butadiene exposed Collaborative Cross mice reflects metabolic phenotype of human lung cancer.</name><description>1,3-Butadiene (BD) exposure is known to cause numerous adverse health effects, including cancer, in animals and humans. BD is metabolized to reactive epoxide intermediates, which are genotoxic, but it is not well know what other effects BD has on cellular metabolism. We examined the effects of exposure to BD on the mouse lung metabolome in the genetically heterogeneous collaborative cross outbred mouse model. Mice were exposed to 3 concentra-tions of BD for 10 days (2, 20, and 200 ppm), and lung tissues were analyzed using high-resolution mass spectrometry-based metabolomics. As compared to controls (0 ppm BD), BD had extensive effects on lung metabolism at all concentrations of exposure, including the lowest concentration of 2 ppm, as reflected by reprogramming of multiple metabolic pathw</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-18T13:24:10.508Z</modification><creation>2025-02-19T01:30:39.001Z</creation></dates><accession>S-EPMC9062885</accession><cross_references><pubmed>34648870</pubmed><doi>10.1016/j.tox.2021.152987</doi></cross_references></HashMap>