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Differential Gene Expression Induced by Two Genotoxic N-nitroso Carcinogens, Phenobarbital and Ethanol in Mouse Liver Examined with Oligonucleotide Microarray and Quantitative Real-time PCR

机译:寡核苷酸芯片和实时荧光定量PCR检测两种遗传毒性N-亚硝基致癌物苯巴比妥和乙醇在小鼠肝脏中的差异基因表达

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References(28) Cited-By(7) It is known that genotoxic N-nitroso carcinogens induce DNA damage in mouse liver within a few hours and induce mutations within 28 days after their administration. However, related-gene expression changes at these time points in liver were not fully elucidated. Differential gene expression induced by two genotoxic N-nitroso carcinogens in mouse liver was examined 4 h and 28 days after their administration with in-house oligonucleotide microarray (268 genes) and quantitative real-time PCR, and compared to that of a non-genotoxic carcinogen and a non-carcinogenic toxin. Diethylnitrosamine (DEN, 80 mg/kg bw), dipropylnitrosamine (DPN, 250 mg/kg bw), phenobarbital sodium (30 mg/kg bw) and ethanol (1000 mg/kg bw) were injected intraperitoneally into groups of male 9-week-old B6C3F1 mice and liver was dissected after 4 h and 28 days. mRNA from pooled livers was reverse-transcribed to cDNA, and Cy3- and Cy5-labeled cDNA was competitively hybridized with in-house made microarray, scanned and analyzed; additionally, quantitative real-time PCR was performed for selected genes. Differential gene expression between two genotoxic N-nitroso carcinogens and phenobarbital and ethanol was observed in 11 genes 4 h after administration, including seven tumor suppressor p53 target genes, viz. c-Jun, Ccng1, Mdm2, p21, Bax, Hsp27 and Snk; the other genes were Mbd1, Hmox-1, Ccnf and Rad52. However, only some degree of differential gene expression of p21, Ccng1 and Snk was observed 28 days after administration; no other differentially-expressed genes were evident. The present results suggest that DEN and DPN induce differential gene expression in p53 target genes in liver within a few hours after administration and that these acute responses remained only partially in liver after 28 days.
机译:参考文献(28)被引依据(7)已知,遗传毒性N-亚硝基致癌物在给药后数小时内会在小鼠肝脏中引起DNA损伤,并在28天内引起突变。但是,尚未完全阐明在这些时间点肝脏中的相关基因表达变化。在使用内部寡核苷酸微阵列(268个基因)和定量实时PCR进行给药后4小时和28天,检查了两种遗传毒性N-亚硝基致癌物在小鼠肝脏中诱导的差异基因表达,并与非遗传毒性进行了比较致癌物和非致癌毒素。将二乙基亚硝胺(DEN,80 mg / kg bw),二丙基亚硝胺(DPN,250 mg / kg bw),苯巴比妥钠(30 mg / kg bw)和乙醇(1000 mg / kg bw)腹膜内注射到男性9周组中4 h和28天后,解剖了B6C3F1型老小鼠和肝脏。将合并肝脏的mRNA反转录为cDNA,然后将Cy3和Cy5标记的cDNA与内部微阵列竞争杂交,进行扫描和分析。另外,对选定的基因进行定量实时PCR。给药后4小时,在11个基因中观察到两种遗传毒性N-亚硝基致癌物与苯巴比妥和乙醇之间的差异基因表达,包括七个抑癌p53靶基因。 c-Jun,Ccng1,Mdm2,p21,Bax,Hsp27和Snk;其他基因是Mbd1,Hmox-1,Ccnf和Rad52。但是,给药后28天仅观察到p21,Ccng1和Snk的某种程度的差异基因表达。没有其他差异表达的基因明显。目前的结果表明,DEN和DPN在给药后数小时内诱导肝中p53靶基因的差异基因表达,并且这些急性反应在28天后仅部分保留在肝中。

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