Casciano D A
Division of Genetic Toxicology, National Center for Toxicological Research, Jefferson, AR 72079.
SAAS Bull Biochem Biotechnol. 1990 Jan;3:102-6.
Hepatocytes were exposed in vitro to the hepatocarcinogen N-hydroxy-2-aminofluorene (N-OH-AAF) in order to determine the nature and repair of DNA adducts formed. N-OH-AAF formed 3 DNA adducts, N-(deoxyguanosin-8yl)-2-acetylaminofluorene (dG-C8-AAF), N-(deoxyguanosin-8-yl)-2-aminofluorene (dG-C8-AF), and 3-(deoxyguanosin-N2-yl)-2-acetylaminofluorene (dG-N2-AAF). The removal of these adducts was measured up to 38 h following cessation of exposure to N-OH-AAF. The dG-C8-AAF adduct was removed with a half-life of about 10 h, while the other two remained relatively constant throughout the incubation period. The dG-C8-AAF adduct is probably responsible for the induction of unscheduled DNA synthesis (UDS) in this model in vitro system.
将肝细胞在体外暴露于肝癌致癌物N-羟基-2-氨基芴(N-OH-AAF),以确定形成的DNA加合物的性质和修复情况。N-OH-AAF形成了3种DNA加合物,即N-(脱氧鸟苷-8-基)-2-乙酰氨基芴(dG-C8-AAF)、N-(脱氧鸟苷-8-基)-2-氨基芴(dG-C8-AF)和3-(脱氧鸟苷-N2-基)-2-乙酰氨基芴(dG-N2-AAF)。在停止暴露于N-OH-AAF后长达38小时内测量这些加合物的去除情况。dG-C8-AAF加合物以约10小时的半衰期被去除,而其他两种在整个孵育期内保持相对恒定。在这个体外模型系统中,dG-C8-AAF加合物可能是诱导非预定DNA合成(UDS)的原因。