001     126916
005     20240228140854.0
024 7 _ |a 10.1016/j.tiv.2014.09.004
|2 doi
024 7 _ |a pmid:25230394
|2 pmid
024 7 _ |a pmc:PMC4258613
|2 pmc
024 7 _ |a 0887-2333
|2 ISSN
024 7 _ |a 1879-3177
|2 ISSN
024 7 _ |a altmetric:2693978
|2 altmetric
037 _ _ |a DKFZ-2017-02944
041 _ _ |a eng
082 _ _ |a 610
100 1 _ |a Krais, Annette M
|b 0
245 _ _ |a Comparison of the metabolic activation of environmental carcinogens in mouse embryonic stem cells and mouse embryonic fibroblasts.
260 _ _ |a Amsterdam [u.a.]
|c 2015
|b Elsevier Science
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1522309540_19820
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a We compared mouse embryonic stem (ES) cells and fibroblasts (MEFs) for their ability to metabolically activate the environmental carcinogens benzo[a]pyrene (BaP), 3-nitrobenzanthrone (3-NBA) and aristolochic acid I (AAI), measuring DNA adduct formation by (32)P-postlabelling and expression of xenobiotic-metabolism genes by quantitative real-time PCR. At 2 μM, BaP induced Cyp1a1 expression in MEFs to a much greater extent than in ES cells and formed 45 times more adducts. Nqo1 mRNA expression was increased by 3-NBA in both cell types but induction was higher in MEFs, as was adduct formation. For AAI, DNA binding was over 450 times higher in MEFs than in ES cells, although Nqo1 and Cyp1a1 transcriptional levels did not explain this difference. We found higher global methylation of DNA in ES cells than in MEFs, which suggests higher chromatin density and lower accessibility of the DNA to DNA damaging agents in ES cells. However, AAI treatment did not alter DNA methylation. Thus mouse ES cells and MEFs have the metabolic competence to activate a number of environmental carcinogens, but MEFs have lower global DNA methylation and higher metabolic capacity than mouse ES cells.
536 _ _ |a 315 - Imaging and radiooncology (POF3-315)
|0 G:(DE-HGF)POF3-315
|c POF3-315
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a 3-nitrobenzanthrone
|2 NLM Chemicals
650 _ 7 |a Aristolochic Acids
|2 NLM Chemicals
650 _ 7 |a Benz(a)Anthracenes
|2 NLM Chemicals
650 _ 7 |a Carcinogens, Environmental
|2 NLM Chemicals
650 _ 7 |a DNA Adducts
|2 NLM Chemicals
650 _ 7 |a Benzo(a)pyrene
|0 3417WMA06D
|2 NLM Chemicals
650 _ 7 |a aristolochic acid I
|0 94218WFP5T
|2 NLM Chemicals
700 1 _ |a Mühlbauer, Karl-Rudolf
|0 P:(DE-He78)0a78151e49e9c847ad9e913a5c2b0ffe
|b 1
|u dkfz
700 1 _ |a Kucab, Jill E
|b 2
700 1 _ |a Chinbuah, Helena
|b 3
700 1 _ |a Cornelius, Michael G
|0 P:(DE-HGF)0
|b 4
700 1 _ |a Wei, Quan-Xiang
|0 P:(DE-HGF)0
|b 5
700 1 _ |a Hollstein, Monica
|0 P:(DE-He78)f3bec70c95e9e3dce0f39d54b3843118
|b 6
|u dkfz
700 1 _ |a Phillips, David H
|b 7
700 1 _ |a Arlt, Volker M
|b 8
700 1 _ |a Schmeiser, Heinz
|0 P:(DE-He78)5e6f79f3c71682d052bc2536749ca077
|b 9
|e Last author
|u dkfz
773 _ _ |a 10.1016/j.tiv.2014.09.004
|g Vol. 29, no. 1, p. 34 - 43
|0 PERI:(DE-600)1501079-x
|n 1
|p 34 - 43
|t Toxicology in vitro
|v 29
|y 2015
|x 0887-2333
909 C O |o oai:inrepo02.dkfz.de:126916
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 1
|6 P:(DE-He78)0a78151e49e9c847ad9e913a5c2b0ffe
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 4
|6 P:(DE-HGF)0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 5
|6 P:(DE-HGF)0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 6
|6 P:(DE-He78)f3bec70c95e9e3dce0f39d54b3843118
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 9
|6 P:(DE-He78)5e6f79f3c71682d052bc2536749ca077
913 1 _ |a DE-HGF
|l Krebsforschung
|1 G:(DE-HGF)POF3-310
|0 G:(DE-HGF)POF3-315
|2 G:(DE-HGF)POF3-300
|v Imaging and radiooncology
|x 0
|4 G:(DE-HGF)POF
|3 G:(DE-HGF)POF3
|b Gesundheit
914 1 _ |y 2015
915 _ _ |a Nationallizenz
|0 StatID:(DE-HGF)0420
|2 StatID
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0310
|2 StatID
|b NCBI Molecular Biology Database
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b TOXICOL IN VITRO : 2015
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Thomson Reuters Master Journal List
915 _ _ |a WoS
|0 StatID:(DE-HGF)0110
|2 StatID
|b Science Citation Index
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
915 _ _ |a WoS
|0 StatID:(DE-HGF)0111
|2 StatID
|b Science Citation Index Expanded
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
915 _ _ |a IF < 5
|0 StatID:(DE-HGF)9900
|2 StatID
920 1 _ |0 I:(DE-He78)C016-20160331
|k C016
|l Genetische Veränderungen bei der Karzinogenese
|x 0
920 1 _ |0 I:(DE-He78)E030-20160331
|k E030
|l Radiopharmazeutische Chemie
|x 1
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)C016-20160331
980 _ _ |a I:(DE-He78)E030-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21