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大鼠肝癌细胞系修复O6-甲基鸟嘌呤-DNA的能力与其分化状态相关。

The capacity of rat hepatoma cell lines for O6-methylguanine-DNA repair correlates with their status of differentiation.

作者信息

Hesse S, Mezger M, Wiebel F J

出版信息

Carcinogenesis. 1984 Jul;5(7):975-8. doi: 10.1093/carcin/5.7.975.

Abstract

O6-Methylguanine-DNA methyltransferase activity, i.e., the capacity of cells to transfer the methyl group from O6-methylguanine in DNA to protein, was determined in 10 hepatoma cell lines, all derived from Reuber H35 hepatoma but differing in their status of differentiation. Methyltransferase activity of the six differentiated lines tested was at least 4-5 times higher than that of two dedifferentiated lines. The activity of the two poorly differentiated lines examined was low to intermediate. Some of the differentiated lines possessed methyltransferase activities comparable to those in hepatocytes freshly isolated from adult rat. The results suggest that certain differentiated hepatoma lines are capable of mimicking liver in the capacity for repair of O6-methylguanine lesions and in this respect may be useful as model systems for studying liver-specific effects of monofunctional alkylating agents.

摘要

测定了10种肝癌细胞系中的O6-甲基鸟嘌呤-DNA甲基转移酶活性,即细胞将DNA中O6-甲基鸟嘌呤上的甲基转移至蛋白质的能力,所有这些细胞系均源自鲁伯H35肝癌,但分化状态不同。所检测的6种分化细胞系的甲基转移酶活性至少比2种去分化细胞系高4至5倍。所检测的2种低分化细胞系的活性处于低到中等水平。一些分化细胞系的甲基转移酶活性与从成年大鼠新鲜分离的肝细胞相当。结果表明,某些分化的肝癌细胞系在修复O6-甲基鸟嘌呤损伤的能力方面能够模拟肝脏,在这方面可能作为研究单功能烷化剂肝脏特异性效应的模型系统。

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