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在持续接触二乙基亚硝胺的大鼠肝细胞DNA中,O4-乙基脱氧胸苷会累积,而O6-乙基脱氧鸟苷则不会。

O4-ethyldeoxythymidine, but not O6-ethyldeoxyguanosine, accumulates in hepatocyte DNA of rats exposed continuously to diethylnitrosamine.

作者信息

Swenberg J A, Dyroff M C, Bedell M A, Popp J A, Huh N, Kirstein U, Rajewsky M F

出版信息

Proc Natl Acad Sci U S A. 1984 Mar;81(6):1692-5. doi: 10.1073/pnas.81.6.1692.

Abstract

In previous investigations into the mechanisms responsible for cell specificity in hepatocarcinogenesis, we have demonstrated that O6-methylguanine accumulates in the DNA of nonparenchymal cells (NPC) but is efficiently removed from hepatocellular DNA. O6-Alkylguanine may, therefore, be an important promutagenic lesion responsible for the induction of hepatic angiosarcomas after exposure to methylating agents, but other promutagenic DNA alkylation products--i.e., O4-alkylthymine--may be responsible for the initiation of hepatocellular carcinomas. F-344 male rats were provided drinking water containing diethylnitrosamine (DEN) at 40 ppm for 0, 2, 4, 8, 16, 28, 49, or 77 days, a regimen that selectively causes hepatocellular carcinomas. Hepatocytes and NPC were isolated by using low-speed differential centrifugation. DNA was purified by hydroxyapatite chromatography and hydrolyzed enzymatically, and O4-ethyldeoxythymidine (O4-EtdThd) and O6-ethyldeoxyguanosine (O6-EtdGuo) of hepatocyte and NPC DNA were quantitated by competitive radioimmunoassay using high-affinity monoclonal antibodies. O4-EtdThd accumulated in hepatocyte DNA during the first 28 days of DEN exposure, approximating a steady state at an O4-EtdThd-to-deoxythymidine molar ratio of approximately equal to 1 X 10(-5). This O4-EtdThd concentration was maintained from 28 to 77 days of DEN exposure. In contrast, O6-EtdGuo did not accumulate in hepatocyte DNA, its greatest concentration O6-EtdGuo-to-deoxyguanosine ratio (approximately equal to 3.7 X 10(-7) ) being detected after 2 days of exposure to DEN. O6-EtdGuo concentrations in hepatocyte DNA decreased with duration of exposure to DEN to an O6-EtdGuo-to-deoxyguanosine ratio of less than 2 X 10(-7) from 28 to 77 days. The data indicate that O4-EtdThd disappears from the DNA of hepatocytes less than 1/200th as fast as O6-EtdGuo. DNA from NPC contained approximately half as much O4-EtdThd as hepatocytes did, but greater than or equal to 2.5 times more O6-EtdGuo.

摘要

在先前对肝癌发生过程中细胞特异性机制的研究中,我们已经证明,O6-甲基鸟嘌呤在非实质细胞(NPC)的DNA中积累,但能从肝细胞DNA中有效清除。因此,O6-烷基鸟嘌呤可能是一种重要的促诱变损伤,导致接触甲基化剂后诱发肝血管肉瘤,但其他促诱变DNA烷基化产物——即O4-烷基胸腺嘧啶——可能是肝细胞癌起始的原因。给F-344雄性大鼠提供含40 ppm二乙基亚硝胺(DEN)的饮用水,持续0、2、4、8、16、28、49或77天,该方案可选择性地诱发肝细胞癌。通过低速差速离心分离肝细胞和NPC。通过羟基磷灰石色谱法纯化DNA并进行酶水解,使用高亲和力单克隆抗体通过竞争性放射免疫测定法定量肝细胞和NPC DNA中的O4-乙基脱氧胸腺嘧啶(O4-EtdThd)和O6-乙基脱氧鸟苷(O6-EtdGuo)。在DEN暴露的前28天,O4-EtdThd在肝细胞DNA中积累,在O4-EtdThd与脱氧胸腺嘧啶的摩尔比约为1×10⁻⁵时接近稳定状态。在DEN暴露的28至77天期间,该O4-EtdThd浓度保持不变。相比之下,O6-EtdGuo没有在肝细胞DNA中积累,在暴露于DEN 2天后检测到其最大浓度的O6-EtdGuo与脱氧鸟苷的比率(约为3.7×10⁻⁷)。从28至77天,随着DEN暴露时间的延长,肝细胞DNA中O6-EtdGuo的浓度下降至O6-EtdGuo与脱氧鸟苷的比率小于2×10⁻⁷。数据表明,O4-EtdThd从肝细胞DNA中消失的速度比O6-EtdGuo慢不到1/200。NPC的DNA中O4-EtdThd的含量约为肝细胞的一半,但O6-EtdGuo的含量比肝细胞多2.5倍或更多。

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