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Circular RNAs promote TRPM3 expression by inhibiting hsa-miR-130a-3p in coronary artery disease patients

机译:环状RNA通过抑制hsa-miR-130a-3p在冠心病患者中促进TRPM3表达

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摘要

We investigated the differential expression of circular RNAs (circRNAs) in plasma samples from three coronary artery disease (CAD) patients to identify putative therapeutic targets. We identified 24 differentially expressed circRNAs (18 up-regulated and 6 down-regulated) and 7 differentially expressed mRNAs (6 up-regulated and 1 down-regulated) in CAD patients based on competing endogenous RNA (ceRNA) microarray analysis. MiR-221(p = 0.001), miR-155(p = 0.049), and miR-130a (p = 0.001) were downregulated in CAD patients based on qRT-PCR analysis of another independent population of 932 study subjects (648 CAD subjects and 284 controls). We constructed a hsa-miR-130a-3p-mediated circRNA-mRNA ceRNA network using the miRanda database. This included 9 circRNAs (hsa_circ_0089378, hsa_circ_0083357, hsa_circ_0082824, hsa_circ_0068942, hsa_circ_0057576, hsa_circ_0054537, hsa_circ_0051172, hsa_circ_0032970, and hsa_circ_0006323) and 1 mRNA (transient receptor potential cation channel subfamily M member 3 [TRPM3]). We have shown that 9 circRNAs promote TRPM3 expression by inhibiting hsa-miR-130a-3p in CAD patients.
机译:我们调查了来自三名冠状动脉疾病(CAD)患者血浆样品中环状RNA(circRNA)的差异表达,以确定推定的治疗靶标。基于竞争内源RNA(ceRNA)微阵列分析,我们在CAD患者中鉴定了24个差异表达的circRNA(18个上调和6个下调)和7个差异表达的mRNA(6个上调和1个下调)。根据对另外932个研究对象的独立人群(648个CAD受试者)的qRT-PCR分析,在CAD患者中下调了MiR-221(p = 0.001),miR-155(p = 0.049)和miR-130a(p = 0.001)。和284个控件)。我们使用miRanda数据库构建了一个hsa-miR-130a-3p介导的circRNA-mRNA ceRNA网络。其中包括9个circRNA(hsa_circ_0089378,hsa_circ_0083357,hsa_circ_0082824,hsa_circ_0068942,hsa_circ_0057576,hsa_circ_0054537,hsa_circ_0051172,hsa_circ_0032970和hsa_circ_0006323)和1个mRNA(瞬时受体电位阳离子通道3TR3)。我们已经显示,有9种circRNA通过抑制CAD患者中的hsa-miR-130a-3p来促进TRPM3表达。

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