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咖啡因对用乙基亚硝基脲处理后的细胞杀伤、诱变、DNA修复及DNA合成的影响。

Effect of caffeine on cell killing, mutation induction, DNA repair, and DNA synthesis after treatment with ethylnitrosourea.

作者信息

Goth-Goldstein R, Painter R B

出版信息

Carcinogenesis. 1981;2(12):1267-71. doi: 10.1093/carcin/2.12.1267.

Abstract

The effect of caffeine on cell killing, mutation induction, DNA repair, and inhibition of DNA synthesis was investigated in a clonal derivative of M3-1 Chinese hamster cells after treatment with N-ethyl-N-nitrosourea (ENU). Caffeine enhanced cell killing but had no effect on the mutation frequency/viable cells for the two genetic markers, 6-thioguanine resistance and ouabain resistance. The removal of ethylated purine bases from DNA was as follows: most of the 3-ethyladenine was lost in 20 h (greater than 85%) and approximately 45% of the 7-ethylguanine was lost in 45 h, whereas 75--93% of the O6-ethylguanine was still present at this time. Caffeine did not seem to influence these rates significantly. The ENU-induced inhibition of DNA synthesis was reversed by caffeine. It is concluded that the potentiation of ENU-induced cell killing by caffeine is caused by the increased frequency of DNA replication past damaged sites in parental DNA.

摘要

在用N-乙基-N-亚硝基脲(ENU)处理后,研究了咖啡因对M3-1中国仓鼠细胞的克隆衍生物中细胞杀伤、突变诱导、DNA修复和DNA合成抑制的影响。咖啡因增强了细胞杀伤作用,但对两种遗传标记物(6-硫鸟嘌呤抗性和哇巴因抗性)的突变频率/存活细胞没有影响。从DNA中去除乙基化嘌呤碱基的情况如下:大部分3-乙基腺嘌呤在20小时内丢失(超过85%),约45%的7-乙基鸟嘌呤在45小时内丢失,而此时仍有75%-93%的O6-乙基鸟嘌呤存在。咖啡因似乎没有显著影响这些速率。咖啡因逆转了ENU诱导的DNA合成抑制。结论是,咖啡因增强ENU诱导的细胞杀伤作用是由于亲代DNA中受损位点处DNA复制频率增加所致。

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