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Differential gene expression profiles in peripheral blood inNortheast Chinese Han people with acute myocardial infarction

机译:外周血中差异基因表达谱东北汉族急性心肌梗死

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摘要

This study aimed to use gene chips to investigate differential gene expression profiles in the occurrence and development of acute myocardial infarction (AMI). The study included 12 AMI patients and 12 healthy individuals. Total mRNA of peripheral bloodwas extracted and reversed-transcribed to cDNA for microarray analysis. After establishing two pools with three subjects each (3 AMI patients and 3 healthy individuals), the remaining samples were used for RT-qPCR to confirm the microarray data. From the microarray results, seven genes were randomly selected for RT-qPCR. RT-qPCR results were analyzed by the 2-ΔΔCt method. Microarray analysis showed that 228 genes were up- regulated and 271 were down-regulated (p ≤ 0.05, |logFC| > 1). Gene ontology showed that these genes belong to 128 cellular components, 521 biological processes, and 151 molecular functions. KEGG pathway analysis showed that these genes are involved in 107 gene pathways. RT-qPCR results for the seven genes showed expression levels consistent with those obtained by microarray. Thus, microarray data could be used to select the pathogenic genes for AMI. Investigating the abnormal expression of these differentially expressed genes might suggest efficient strategies for the prevention, diagnosis, andtreatment of AMI.
机译:这项研究旨在使用基因芯片来研究急性心肌梗塞(AMI)发生和发展中的差异基因表达谱。该研究包括12名AMI患者和12名健康个体。提取外周血总mRNA并将其逆转录为cDNA以进行微阵列分析。建立两个池,每个池包含三个对象(3个AMI患者和3个健康个体)后,将其余样品用于RT-qPCR以确认微阵列数据。从微阵列结果中,随机选择了七个基因用于RT-qPCR。用2 -ΔΔCt方法分析RT-qPCR结果。基因芯片分析显示228个基因被上调,而271个基因被下调(p≤0.05,| logFC |> 1)。基因本体论表明这些基因属于128个细胞成分,521个生物学过程和151个分子功能。 KEGG通路分析表明,这些基因参与了107条基因通路。七个基因的RT-qPCR结果显示表达水平与通过微阵列获得的表达水平一致。因此,微阵列数据可用于选择AMI的致病基因。研究这些差异表达基因的异常表达可能提示预防,诊断和治疗的有效策略。AMI的治疗。

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