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- W2149613746 abstract "Abstract The morphological cell transforming activities of three dihydrodiols of benzo[c]chrysene (B[c]C), trans−B[c]C-7,8-diol, trans−B[c]C-9,10-diol, and trans−B[c]C-1,2-diol were compared to those of B[c]C in order to study the possible routes of metabolic activation in transformable C3H10T1/2 mouse embryo fibroblasts. B[c]C-treated C3H10T1/2 cells exhibited a concentration-related increase in morphologically transformed foci over a concentration range of 0–3 μg/ml. At 3 μg/ml, B[c]C induced 1.23 Type II & III foci/dish, with 73% of the dishes exhibiting Type II or Type III foci, and a survival of 87%. trans−B[c]C-7,8-diol produced concentration-related responses over a range of 0–5 μg/ml. At 3 μg/ml, trans−B[c]C-7,8-diol produced 1.13 Type II & III foci/dish with 72% of the dishes exhibiting foci, and a survival of 76%. trans−B[c]C-9,10-diol was inactive as a morphological cell transforming agent over a concentration range of 0–3 μg/ml. trans−B[c]C-1,2-diol was also inactive as a morphological cell transforming agent over a concentration range of 0–3 μg/ml. These results suggest that a K-region dihydrodiol of B[c]C, trans−B[cC-7,8-diol, may play a role in the ability of B[c]C to morphologically transform C3H10T1/2 cells." @default.
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- W2149613746 date "2000-12-01" @default.
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- W2149613746 title "Evaluation of Benzo[c]Chrysene Dihydrodiols in the Morphological Cell Transformation of Mouse Embryo Fibroblast C3H10T1/2CL8 Cells" @default.
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- W2149613746 doi "https://doi.org/10.1080/10406630008028534" @default.
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