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Analysis of differential expression of hypoxia-inducible microRNA-210 gene targets in mild and severe preeclamptic patients

机译:缺氧诱导微小RONA-210基因靶标在轻度和严重的初期患者中的差异分析

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摘要

Preeclampsia (PE) is a multi-system disorder that is specific to human pregnancy. Inadequate oxygenation of uterus and placenta is considered as one of the leading causes for the disease. MicroRNA-210(miR-210) is one of the prime molecules that has emerged in response to hypoxia. The objective of this study was to determine miR-210 expression patterns in plasma from severe PE and mild PE patients, and how that affects the expression of miR-210 target genes. The expression levels of miR-210 were validated using reverse transcription-quantitative PCR in plasma of severe PE (15) and mild PE (15) patients in comparison to controls subjects (15) with normal pregnancy. Then, the association between miR-210 and its downstream genes was validated by using human miR-210 targets RT2 profiler PCR Array. Both the categories (mild and severe) showed significantly high miR-210 expression levels. Also out of the 84 hypoxia miR-210 associated genes screened using mRNA, 18 genes were found to be differentially expressed in severe PE whereas 16 genes in mild PE cases with varying magnitude. All the genes in both the PE groups were found downregulated in comparison to controls. These downregulated genes expressed in both the cases were shown to be participating in immunosuppression, apoptosis, cell growth, signaling, angiogenesis, DNA repair. This study provides novel data on the genes that work downstream of miR-210 and how dysregulated expression of miR-210 can affect their expression and in turn functioning which can be associated with PE risk and severity. This study is the very first to determine the effect of miR-210 expression levels on associated genes in plasma samples.
机译:Preclampsia(PE)是一种特异于人性妊娠的多系统障碍。子宫和胎盘的不充分氧合被认为是疾病的主要原因之一。 MicroRNA-210(miR-210)是响应缺氧而出现的主要分子之一。本研究的目的是确定来自严重PE和轻度PE患者的血浆中的miR-210表达模式,以及影响miR-210靶基因的表达。使用严重PE(15)和轻度PE(15)患者的血浆中的逆转录定量PCR验证MIR-210的表达水平,与正常妊娠进行对象(15)。然后,通过使用人miR-210靶标RT2分析器PCR阵列验证MIR-210与其下游基因之间的关联。类别(轻度和严重)都显示出明显高的miR-210表达水平。在使用mRNA筛选的84个缺氧miR-210相关基因中,发现18个基因以严重的体积差异表达,而在温和的体积中的16个基因,具有不同的幅度。与对照相比,每种PE组的所有基因都被发现下调。这些案例中表达的这些下调基因显示出参与免疫抑制,细胞凋亡,细胞生长,信号传导,血管生成,DNA修复。该研究提供了关于MIR-210下游的基因的新数据,以及MiR-210的失调表达如何影响它们的表达,并且可以与体育风险和严重程度相关联。该研究是首先确定miR-210表达水平对血浆样品中相关基因的影响。

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