摘要
目的:探讨siRNA对人乳腺癌细胞株SK—BR-3的HER-2/neu基因表达的影响。方法:以HER-2/neu mRNA序列为模板设计合成2对siRNA序列,构建pGenesil-1-HER-2/neusiRNA重组质粒,转化感受态的大肠杆菌,质粒酶切、测序鉴定。转染SK—BR-3细胞48h后,提取RNA进行RT—PCR,采用方差分析(ANOVA),分析RNA干扰效应。结果:成功构建了pGenesil-1-HER-2/neu siRNA重组质粒,成功转染SK—BR-3细胞。重组质粒抑制HER-2/neu基因的表达接近54.45%(P=0.000)。结论:HER-2/neu siRNA重组质粒明显下调HER-2/neu基因在乳腺癌细胞中的表达。
Objective:To investigate the effects of siRNA to HER-2/neu gene of human breast cancer cell line SK-BR-3. Methods: Two pairs of siRNA were designed and synthesized according to the sequence of HER-2/neu mRNA. pGenesil-1-HER-2/neu siRNA recombinant plasmid was then constructed and used to transfected E coll. The constructed plasmids were confirmed by restriction cutting and DNA sequencing. SK-BR-3 cell line was then transfected, and at 48 h later, extracted for total RNA to be detected for expression of HER-2/neu mRNA by RT-PCR. The results was analyzed for gene-silencing effects using ANOVA. Results: pGenesil-l-HER-2/neu siRNA was constructed and SK-BR-3 transfected successfully. RT-PCR analyses found that nearly 54.45% of HER-2/neu mRNA expression in SK-BR-3 was suppressed ( P = 0. 000 ). Conclusions : pGenesil-1-HER-2/neu siRNA may significantly inhibit HER-2/neu gene expression in SK-BR-3.
出处
《广州医学院学报》
2010年第1期6-9,共4页
Academic Journal of Guangzhou Medical College