About: Toxic Effects of Methylated Benzo[a]pyrenes in Rat Liver Stem-Like Cells     Goto   Sponge   NotDistinct   Permalink

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  • AhR-mediated activity of five selected MeBaP isomers was estimated in the DR-CALUX reporter gene assay performed in rat hepatoma cells. We identified 1-MeBaP as the most potent inducer of AhR activation, stable DNA adduct formation, checkpoint kinase 1 and p53 phosphorylation, and apoptosis. These effects suggest that 1-MeBaP is a potent genotoxin eliciting a typical sequence of events ascribed to carcinogenic PAHs. Importantly, 1-MeBaP and 3-MeBaP were found to be potent AhR agonists, 1 order of magnitude more potent than BaP, thus suggesting that the AhR-dependent modulations of gene expression, deregulation of cell survival mechanisms, and further nongenotoxic effects associated with AhR activation may further contribute to their tumor promotion and carcinogenicity.
  • AhR-mediated activity of five selected MeBaP isomers was estimated in the DR-CALUX reporter gene assay performed in rat hepatoma cells. We identified 1-MeBaP as the most potent inducer of AhR activation, stable DNA adduct formation, checkpoint kinase 1 and p53 phosphorylation, and apoptosis. These effects suggest that 1-MeBaP is a potent genotoxin eliciting a typical sequence of events ascribed to carcinogenic PAHs. Importantly, 1-MeBaP and 3-MeBaP were found to be potent AhR agonists, 1 order of magnitude more potent than BaP, thus suggesting that the AhR-dependent modulations of gene expression, deregulation of cell survival mechanisms, and further nongenotoxic effects associated with AhR activation may further contribute to their tumor promotion and carcinogenicity. (en)
Title
  • Toxic Effects of Methylated Benzo[a]pyrenes in Rat Liver Stem-Like Cells
  • Toxic Effects of Methylated Benzo[a]pyrenes in Rat Liver Stem-Like Cells (en)
skos:prefLabel
  • Toxic Effects of Methylated Benzo[a]pyrenes in Rat Liver Stem-Like Cells
  • Toxic Effects of Methylated Benzo[a]pyrenes in Rat Liver Stem-Like Cells (en)
skos:notation
  • RIV/68081707:_____/11:00365862!RIV12-AV0-68081707
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA525/08/1590), Z(AV0Z50040702), Z(AV0Z50390512), Z(MZE0002716202)
http://linked.open...iv/cisloPeriodika
  • 6
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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http://linked.open...dnocenehoVysledku
  • 235646
http://linked.open...ai/riv/idVysledku
  • RIV/68081707:_____/11:00365862
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Ah receptor; DNA adducts; WB F344 cells (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [20D58962D718]
http://linked.open...i/riv/nazevZdroje
  • Chemical Research in Toxicology
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
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http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 24
http://linked.open...iv/tvurceVysledku
  • Ciganek, M.
  • Krčmář, P.
  • Machala, M.
  • Marvanová, S.
  • Milcová, Alena
  • Neča, J.
  • Pěnčíková, K.
  • Topinka, Jan
  • Vondráček, Jan
  • Trilecová, L.
  • Hulínková, P.
  • Krčková, S.
  • Pálková, L.
http://linked.open...ain/vavai/riv/wos
  • 000291896700011
http://linked.open...n/vavai/riv/zamer
issn
  • 0893-228X
number of pages
http://bibframe.org/vocab/doi
  • 10.1021/tx200049x
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