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The resveratrol analogue, 2,3′,4,5′-tetramethoxystilbene, does not inhibit CYP gene expression, enzyme activity and benzo[a]pyrene–DNA adduct formation in MCF-7 cells exposed to benzo[a]pyrene
Exposure to carcinogenic polycyclic aromatic hydrocarbons (PAHs) induces cytochrome P450 (CYP) 1A1 and 1B1 enzymes, which biotransform PAHs resulting in the formation of DNA adducts. We hypothesised that 2,3′,4,5′-tetramethoxystilbene (TMS), an analogue of resveratrol and a potent CYP1B1 inhibitor,...
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主要な著者: | , , |
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フォーマット: | Artigo |
言語: | Inglês |
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Oxford University Press
2011
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オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3162036/ https://ncbi.nlm.nih.gov/pubmed/21669939 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/mutage/ger024 |
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