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首页> 外文期刊>Cardiovascular Diabetology >No detectable differential microRNA expression between non-atherosclerotic arteries of type 2 diabetic patients (treated or untreated with metformin) and non-diabetic patients
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No detectable differential microRNA expression between non-atherosclerotic arteries of type 2 diabetic patients (treated or untreated with metformin) and non-diabetic patients

机译:2型糖尿病患者(用二甲双胍治疗或未治疗)和非糖尿病患者的非动脉粥样硬化动脉之间未检测到差异性microRNA表达

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Type 2 diabetes mellitus (T2DM) is an independent risk factor of cardiovascular disease (CVD), however, the underlying mechanisms are largely unknown. Using non-atherosclerotic internal thoracic arteries (ITAs) obtained from coronary artery bypass grafting, we previously identified a distinct elevation in the level of proteins comprising the arterial basement membrane in T2DM patients not treated with metformin. Altered transcription of genes encoding these proteins has not been observed, indicating alternative mechanisms of dysregulation. In this study we screened for differential expression of arterial microRNAs (miRNAs) in T2DM patients to test the hypothesis that the arterial protein signature of diabetic patients is associated with dysregulation at the miRNA level, and further to lay the foundation for novel hypotheses addressing the increased CVD risk of T2DM patients. MiRNA isolated from fresh frozen ITAs [from 18 T2DM- (10 of which were subject to metformin treatment) and 30 non-diabetes mellitus (non-DM) patients] were analyzed by microarray, and miRNAs isolated from formalin-fixated paraffin-embedded (FFPE) ITAs were analyzed by quantitative PCR (qPCR) in an independent study group [26 T2DM- (15 of which were subject to metformin treatment) and 26 non-DM patients] to determine expression levels of miRNAs in a pre-defined panel of 12 miRNAs. Unexpectedly, no miRNAs were found to be affected by T2DM status in either of the two study groups. Our data suggest that alternatives to microRNA dysregulation underlie T2DM-associated protein changes in non-atherosclerotic arteries.
机译:2型糖尿病(T2DM)是心血管疾病(CVD)的独立危险因素,但是其基本机制尚不清楚。使用从冠状动脉搭桥术获得的非动脉粥样硬化性胸腔内动脉(ITAs),我们先前在未接受二甲双胍治疗的T2DM患者中发现了构成动脉基底膜的蛋白质水平明显升高。尚未观察到编码这些蛋白质的基因的转录改变,这表明异常调节的替代机制。在这项研究中,我们筛选了T2DM患者中动脉microRNA(miRNA)的差异表达,以检验以下假设:糖尿病患者的动脉蛋白签名与miRNA水平的调节异常有关,并进一步为解决假说增加的新假设奠定了基础T2DM患者的CVD风险。通过微阵列分析从新鲜冷冻ITAs(从18例T2DM-(其中10例接受二甲双胍治疗)和30例非糖尿病(非DM)患者中分离出的miRNA),以及从福尔马林固定石蜡包埋的( FFPE)在独立研究组[26名T2DM-(其中15名接受二甲双胍治疗)和26名非DM患者]中通过定量PCR(qPCR)分析了ITA,以确定miRNA在预定义组中的表达水平。 12个miRNA。出乎意料的是,两个研究组中的任何一个都没有发现miRNA受T2DM状态的影响。我们的数据表明,microRNA失调的替代方法是非动脉粥样硬化动脉中T2DM相关蛋白变化的基础。

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