Qian Yating, Lu Yuanqing, Rui Can, Qian Yujia, Cai Manhong, Jia Ruizhe
Department of Obstetrics, Nanjing Medical University Affiliated Nanjing Maternal and Child Health Hospital, Nanjing, China.
Cell Physiol Biochem. 2016;39(4):1380-90. doi: 10.1159/000447842. Epub 2016 Sep 8.
This study aimed to identify the different expression of circular RNAs (circRNAs) in the placental tissues of pregnant women with preeclampsia (PE) and to provide a new avenue of research regarding the pathological mechanisms of PE.
In this study, we collected 40 placental tissues from PE patients and 35 placental tissues from gestational age-matched patients who gave premature birth. Arraystar circRNA Microarray Technology (KANGCHEN, Shanghai, China) was used to analyze the differential expression of circRNAs. According to the basic content of circRNAs in the two groups and their fold changes and due to the practicability of the designed divergent primers of each candidate circRNA, we selected three up-regulated circRNAs, hsa_circRNA_100782, hsa_circRNA_102682 and hsa_circRNA_104820, to validate the data. Real-time quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) was utilized to estimate the Ct values in both groups. We further evaluated the differences with a paired t-test and a receiver operating characteristic (ROC) curve.
Many circRNAs were found to be differentially expressed in PE placental tissues versus their controls; of these, 143 circRNAs were up-regulated and 158 were down-regulated. The expression levels of hsa_circRNA_100782 (p < 0.05), hsa_circRNA_102682 (p < 0.05), and hsa_circRNA_104820 (p < 0.0001) were validated as significantly up-regulated in the experimental group compared with the controls. Finally, we performed a literature comparison to forecast the possible mechanisms of circRNA function during PE.
circRNA expression significantly differed in placental PE tissues compared with controls. According to the circRNA microarray results and the existing papers, circRNAs may contribute to the pathogenesis of PE by acting as miRNA sponges; this possibility requires additional investigation in future studies.
本研究旨在鉴定子痫前期(PE)孕妇胎盘组织中环状RNA(circRNA)的差异表达,并为PE的病理机制提供新的研究途径。
在本研究中,我们收集了40例PE患者的胎盘组织和35例孕周匹配的早产患者的胎盘组织。使用Arraystar circRNA微阵列技术(中国上海康成)分析circRNA的差异表达。根据两组中circRNA的基本含量及其倍数变化,并考虑到每个候选circRNA设计的发散引物具有实用性,我们选择了三个上调的circRNA,即hsa_circRNA_100782、hsa_circRNA_102682和hsa_circRNA_104820,来验证数据。利用实时定量逆转录聚合酶链反应(qRT-PCR)来估计两组的Ct值。我们进一步采用配对t检验和受试者工作特征(ROC)曲线评估差异。
发现许多circRNA在PE胎盘组织与其对照组织中存在差异表达;其中,143个circRNA上调,158个circRNA下调。与对照组相比,实验组中hsa_circRNA_100782(p < 0.05)、hsa_circRNA_102682(p < 0.05)和hsa_circRNA_104820(p < 0.0001)的表达水平被证实显著上调。最后,我们进行了文献比较,以预测circRNA在PE过程中发挥功能的可能机制。
与对照组相比,circRNA在胎盘PE组织中的表达存在显著差异。根据circRNA微阵列结果和现有文献,circRNA可能通过充当miRNA海绵促进PE的发病机制;这种可能性需要在未来的研究中进一步探讨。