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Molecular Dosimetry of Endogenous and Exogenous O(6)-Methyl-dG and N7-Methyl-G Adducts Following Low Dose [D(3)]-Methylnitrosourea Exposures in Cultured Human Cells

[Image: see text] For DNA-reactive chemicals, a low dose linear assessment of cancer risk is the science policy default. In the present study, we quantitated the endogenous and exogenous N7-methyl-G and O(6)-methyl-dG adducts in human lymphoblastoid cells exposed to low dose [D(3)]-methylnitrosourea...

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Detalles Bibliográficos
Autores principales: Sharma, Vyom, Collins, Leonard B., Clement, Jean M., Zhang, Zhenfa, Nakamura, Jun, Swenberg, James A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998766/
https://www.ncbi.nlm.nih.gov/pubmed/24628573
http://dx.doi.org/10.1021/tx5000602
Descripción
Sumario:[Image: see text] For DNA-reactive chemicals, a low dose linear assessment of cancer risk is the science policy default. In the present study, we quantitated the endogenous and exogenous N7-methyl-G and O(6)-methyl-dG adducts in human lymphoblastoid cells exposed to low dose [D(3)]-methylnitrosourea. Endogenous amounts of both adducts remained nearly constant, while the exogenous adducts showed linear dose-responses. The data show that O(6)-methyl-dG adducts ≥1.8/10(8) dG correlated with published studies that demonstrated significant increases of mutations under these conditions. The combined results do not support linear extrapolations to zero when data are available for science-based regulations.