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在喂食二甲基亚硝胺的大鼠肝脏血管肉瘤发生过程中DNA损伤的持续性

Persistence of DNA damage during development of liver angiosarcoma in rats fed dimethylnitrosamine.

作者信息

Abanobi S E, Farber E, Sarma D S

出版信息

Cancer Res. 1979 May;39(5):1592-6.

PMID:570883
Abstract

Chronic feeding of a diet containing dimethylnitrosamine (50 ppm) to rats resulted in liver DNA damage monitored as slow sedimentation of the DNA compared to that of the control in alkaline sucrose gradients. The damage in rat liver DNA could be seen within 2 days after beginning the feeding of diets containing the carcinogen and was progressive with the time of feeding, up to 8 weeks. Extended feeding up to 15 or 31 weeks did not result in a proportionate increase in the damage to the DNA. The DNA damage observed at 8 weeks persisted until 31 weeks, at which time liver angiosarcoma was present. Despite the fact that the DNA damage induced by dimethylnitrosamine appears to involve the bulk of the liver DNA, the tumors developed were entirely from vascular endothelium. The implication of these results in the initiation of carcinogenesis is discussed.

摘要

给大鼠长期喂食含二甲基亚硝胺(50 ppm)的饲料,导致肝脏DNA损伤,在碱性蔗糖梯度中,与对照组相比,DNA沉降缓慢可作为监测指标。在开始喂食含致癌物的饲料后2天内,即可观察到大鼠肝脏DNA损伤,且随着喂食时间的延长,这种损伤持续加重,直至8周。延长喂食至15周或31周,并未导致DNA损伤成比例增加。8周时观察到的DNA损伤一直持续到31周,此时肝脏血管肉瘤已经出现。尽管二甲基亚硝胺诱导的DNA损伤似乎涉及大部分肝脏DNA,但所形成的肿瘤完全来源于血管内皮。文中讨论了这些结果在致癌作用起始过程中的意义。

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