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5-氟尿嘧啶掺入小鼠骨髓细胞DNA后的DNA修复

DNA repair following incorporation of 5-fluorouracil into DNA of mouse bone marrow cells.

作者信息

Schuetz J D, Wallace H J, Diasio R B

机构信息

Department of Pharmacology and Comprehensive Cancer Center, University of Alabama, Birmingham 35294.

出版信息

Cancer Chemother Pharmacol. 1988;21(3):208-10. doi: 10.1007/BF00262771.

Abstract

5-Fluorouracil (FUra) was previously demonstrated to be incorporated into DNA at cytotoxic concentrations in mouse bone marrow cells. Subsequently, we showed that under these conditions FUra exhibited a time-dependent removal from DNA accompanied by a decrease in DNA strand length. In the present study we utilized hydroxyurea to inhibit semiconservative DNA synthesis while monitoring DNA repair by measuring the incorporation of [3H]dThd into double-stranded DNA (DNAds), which can be separated from DNA at the replication fork (DNAss) by benzoylated-naphthoylated-DEAE cellulose. Under these conditions we assessed DNA repair in cells that had previously been exposed for 1 h to varying cytotoxic concentrations of FUra. The results demonstrate an increase in labelling of DNAds with increasing FUra concentrations, with no appreciable increase in incorporation of label into DNAss. In conclusion, this study demonstrates that DNA repair occurs following incorporation of FUra. The failure to repair DNA damage at higher FUra concentrations may have a role in the cytotoxicity of this drug.

摘要

5-氟尿嘧啶(FUra)先前已被证明在小鼠骨髓细胞中,在细胞毒性浓度下会掺入DNA。随后,我们表明在这些条件下,FUra从DNA中呈现出时间依赖性的去除,并伴随着DNA链长度的减少。在本研究中,我们利用羟基脲抑制半保留DNA合成,同时通过测量[3H]dThd掺入双链DNA(DNAds)来监测DNA修复,DNAds可通过苯甲酰化-萘甲酰化-DEAE纤维素与复制叉处的DNA(DNAss)分离。在这些条件下,我们评估了先前暴露于不同细胞毒性浓度的FUra 1小时的细胞中的DNA修复情况。结果表明,随着FUra浓度的增加,DNAds的标记增加,而标记掺入DNAss中没有明显增加。总之,本研究表明FUra掺入后会发生DNA修复。在较高FUra浓度下未能修复DNA损伤可能在该药物的细胞毒性中起作用。

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