Zhang Yabing, Cao Ai-Lin, Dong Chun
Department of Cardiology, The First people's Hospital of Jining, Jining, Shandong, China (mainland).
Department of Cardiology, Affiliated Hospital of Jining Medical College, Jining, Shandong, China (mainland).
Med Sci Monit. 2017 Feb 19;23:911-918. doi: 10.12659/msm.897607.
BACKGROUND MiR-27b is reportedly involved with many diseases (e.g., gastric cancer) by acting on different signaling pathways. In this study, we aimed at understanding the relationship between miR-27b and hypertension and its underlying molecular mechanism. MATERIAL AND METHODS Peripheral blood was collected from patients with hypertension, and statistical analysis was performed to study the association between rs10719 and risk of hypertension. Tissue samples were collected from patients with lung cancer, and the expression of miR-27b and DROSHA was determined using Western blot analysis and real-time PCR. RESULTS We first searched the miRNA database online, and identified DROSHA as a virtual target of miR-27b with the "seed sequence" located within the 3'-UTR of the target gene, and then validated DROSHA to be the direct gene via luciferase reporter assay system. We also established the negative regulatory relationship between miR-27b and DROSHA via studying the relative luciferase activity. We also conducted real-time PCR to study the mRNA and protein expression level of miR-27b among different groups. Furthermore, we conducted real-time PCR and densitometry analysis to study the mRNA and protein expression level of DROSHA among different groups of cells treated with scramble control, miR-27b mimics, DROSHA siRNA, and miR-27b inhibitors to verify the negative regulatory relationship between MiR-27b and DROSHA. CONCLUSIONS The presence of rs10719 disrupted the interaction between miR-27b and DROSHA, which might be the underlying mechanism of the observation that rs10719 is significantly associated with risk of primary hypertension.
背景 据报道,MiR-27b通过作用于不同的信号通路参与多种疾病(如胃癌)。在本研究中,我们旨在了解MiR-27b与高血压之间的关系及其潜在的分子机制。
材料与方法 收集高血压患者的外周血,进行统计分析以研究rs10719与高血压风险之间的关联。收集肺癌患者的组织样本,使用蛋白质印迹分析和实时荧光定量PCR测定MiR-27b和DROSHA的表达。
结果 我们首先在线搜索miRNA数据库,通过“种子序列”位于靶基因3'-UTR内,将DROSHA鉴定为MiR-27b的虚拟靶标,然后通过荧光素酶报告基因检测系统验证DROSHA是直接作用的基因。我们还通过研究相对荧光素酶活性建立了MiR-27b与DROSHA之间的负调控关系。我们还进行了实时荧光定量PCR,以研究不同组中MiR-27b的mRNA和蛋白质表达水平。此外,我们进行了实时荧光定量PCR和光密度分析,以研究用乱序对照、MiR-27b模拟物、DROSHA siRNA和MiR-27b抑制剂处理的不同组细胞中DROSHA的mRNA和蛋白质表达水平,以验证MiR-27b与DROSHA之间的负调控关系。
结论 rs10719的存在破坏了MiR-27b与DROSHA之间的相互作用,这可能是rs10719与原发性高血压风险显著相关这一观察结果的潜在机制。