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The expression of Phase II drug-metabolizing enzymes in human B-lymphoblastoid TK6 cells.
Li, Xilin; Li, Yuxi; Ning, Kylie G; Chen, Si; Guo, Lei; Bonzo, Jessica A; Mei, Nan.
Afiliación
  • Li X; Division of Genetic and Molecular Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, USA.
  • Li Y; Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, USA.
  • Ning KG; Division of Genetic and Molecular Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, USA.
  • Chen S; Krieger School of Arts and Sciences, Johns Hopkins University, Baltimore, MD, USA.
  • Guo L; Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, USA.
  • Bonzo JA; Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, USA.
  • Mei N; Division of Pharmacology/Toxicology for Immunology and Inflammation, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD, USA.
Article en En | MEDLINE | ID: mdl-35895929
ABSTRACT
In vitro genotoxicity testing plays an important role in chemical risk assessment. The human B-lymphoblastoid cell line TK6 is widely used as a standard cell line for regulatory safety evaluations. Like many other mammalian cell lines, TK6 cells have limited metabolic capacity; therefore, usually require a source of exogenous metabolic activation for use in genotoxicity testing. Previously, we developed a set of TK6-derived cell lines that individually express one of fourteen cytochrome P450s (CYPs). In the present study, we surveyed a panel of major Phase II drug-metabolizing enzymes to characterize their baseline expression in TK6 cells. These results may serve as a reference enzymatic profile of this commonly used cell line.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Daño del ADN / Mamíferos Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: J Environ Sci Health C Toxicol Carcinog Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Daño del ADN / Mamíferos Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: J Environ Sci Health C Toxicol Carcinog Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos