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首页> 外文期刊>Chinese Medical Journal >Effect of N, N' -dinitrosopiperazine on in vitro expression of human cytochrome P450 2E1
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Effect of N, N' -dinitrosopiperazine on in vitro expression of human cytochrome P450 2E1

机译:N,N'-二亚硝基哌嗪对人细胞色素P450 2E1体外表达的影响

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摘要

Objective To establish an in vitro heterogeneous expression model of human CYP2E1 (hCYP2E1) cDNA and investigate the effect of the chemical carcinogenic N, N'-dinitrosopiperazine (DNP) on the expression of CYP2E1. Methods Exogenous hCYP2E1 was introduced into the mouse derived NIH3T3 cells using the lipofectamine transfection technique. Integration of exogenous hCYP2E1 gene was identified by PCR and Southern blot. After treatment with various concentration of ethanol and DNP on the transfected NIH3T3 cell cultures, RT-PCR and Western blot was applied to detect the expression level of CYP2E1. Results Two cell clones with integration and stable expression of exogenous hCYP2E1 were obtained and designated as NIH3T3-2E1-A4 and NIH3T3-2E1-A8 respectively. The expression of both hCYP2E1 mRNA and protein products was promoted after either ethanol or DNP treatment. Conclusion The results suggested that the promoted expression of hCYP2E1 induced by DNP and/or ethanol is due to enhanced transcription. The mechanism of DNP carcinogenesis might be related to this in situ activated metabolism by CYP2E1.
机译:目的建立人CYP2E1(hCYP2E1)cDNA的体外异源表达模型,探讨化学致癌性N,N'-二亚硝基哌嗪(DNP)对CYP2E1表达的影响。方法采用脂转染胺转染技术,将外源hCYP2E1导入小鼠源性NIH3T3细胞。通过PCR和Southern印迹鉴定外源hCYP2E1基因的整合。在转染的NIH3T3细胞培养物中用不同浓度的乙醇和DNP处理后,采用RT-PCR和Western blot检测CYP2E1的表达水平。结果获得两个整合并稳定表达外源hCYP2E1的细胞克隆,分别命名为NIH3T3-2E1-A4和NIH3T3-2E1-A8。乙醇或DNP处理后均能促进hCYP2E1 mRNA和蛋白产物的表达。结论结果表明,DNP和/或乙醇诱导hCYP2E1的表达增强是由于转录增强。 DNP致癌的机制可能与CYP2E1的这种原位活化代谢有关。

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