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在仓鼠中用肼或二甲基亚硝胺诱导肝癌过程中DNA鸟嘌呤的甲基化。

Methylation of DNA guanine during the course of induction of liver cancer in hamsters by hydrazine or dimethylnitrosamine.

作者信息

Bosan W S, Shank R C, MacEwen J D, Gaworski C L, Newberne P M

出版信息

Carcinogenesis. 1987 Mar;8(3):439-44. doi: 10.1093/carcin/8.3.439.

Abstract

Hydrazine is carcinogenic to the mouse and rat, but three earlier studies have reported no carcinogenicity of hydrazine in the hamster. Administration of hydrazine to mice, rats and hamsters results in rapid methylation of liver DNA guanine for which endogenous formaldehyde appears to be the source of the methyl moiety. Hamsters were given hydrazine sulfate at 170, 340 and 510 mg/l in the drinking water for 2 years [average dose of 4.6, 8.3 and 10.3 mg hydrazine (free base)/kg body wt over the 2-year period], during which levels of methylation of DNA guanine in liver, kidney and lung, and histopathologic examinations of these tissues were carried out; dimethylnitrosamine, as a positive control, was administered at 10 mg/l in the drinking water (average dose of 1.1 mg/kg body wt over the 4-month measurement period). Both 7-methylguanine and O6-methylguanine were readily detectable at 6 months exposure in hamsters given hydrazine or dimethylnitrosamine; in hydrazine-treated animals only trace amounts of these bases could be detected after 12 months exposure; these bases were again detected in liver DNA at exposure times of 18 and 24 months. Hepatocellular carcinomas were observed in hamsters treated at the highest dose of hydrazine sulfate after 78 weeks of exposure; the incidence of liver cancer was dose-related over the course of the experiment: 32% for hamsters exposed to 510 mg hydrazine sulfate/l, 12% for 340 mg/l and none at 170 mg/l. Hamsters given dimethylnitrosamine developed high levels of 7-methylguanine and even higher levels of O6-methylguanine and both liver cholangiocellular carcinomas (73% incidence), as reported before, and hepatocellular carcinomas (27% incidence), a new finding. These results demonstrate for the first time that hydrazine is a liver carcinogen in the hamster and provide new information regarding the accumulation of DNA damage during the entire induction period for the carcinomas.

摘要

肼对小鼠和大鼠具有致癌性,但此前有三项研究报告称肼对仓鼠无致癌性。给小鼠、大鼠和仓鼠施用肼会导致肝脏DNA鸟嘌呤迅速甲基化,内源性甲醛似乎是甲基部分的来源。给仓鼠饮用含170、340和510 mg/l硫酸肼的水,持续2年[在2年期间,平均剂量分别为4.6、8.3和10.3 mg肼(游离碱)/kg体重],在此期间,对肝脏、肾脏和肺中DNA鸟嘌呤的甲基化水平以及这些组织进行组织病理学检查;作为阳性对照,给仓鼠饮用含10 mg/l二甲基亚硝胺的水(在4个月的测量期内,平均剂量为1.1 mg/kg体重)。在接触肼或二甲基亚硝胺6个月的仓鼠中,7-甲基鸟嘌呤和O6-甲基鸟嘌呤都很容易检测到;在接触肼的动物中,接触12个月后只能检测到微量的这些碱基;在接触18个月和24个月时,这些碱基再次在肝脏DNA中被检测到。在接触78周后,观察到接受最高剂量硫酸肼治疗的仓鼠发生了肝细胞癌;在实验过程中,肝癌的发病率与剂量相关:接触510 mg硫酸肼/l的仓鼠为32%,340 mg/l的为12%,170 mg/l的无一发病。如前所述,给仓鼠施用二甲基亚硝胺后,7-甲基鸟嘌呤水平较高,O6-甲基鸟嘌呤水平更高,同时出现了肝胆管细胞癌(发病率73%)和肝细胞癌(发病率27%)这一新发现。这些结果首次证明肼是仓鼠的肝脏致癌物,并提供了关于癌症整个诱导期DNA损伤积累的新信息。

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