Jayaram Hari, Phillips Jay I, Lozano Diana C, Choe Tiffany E, Cepurna William O, Johnson Elaine C, Morrison John C, Gattey Devin M, Saugstad Julie A, Keller Kate E
Glaucoma Service, National Institute for Health Research, Biomedical Research Centre for Ophthalmology, UCL Institute of Ophthalmology & Moorfields Eye Hospital, London, United Kingdom 2Casey Eye Institute, Oregon Health & Science University, Portland, Oregon, United States.
Anesthesiology & Perioperative Medicine, Oregon Health & Science University, Portland, Oregon, United States.
Invest Ophthalmol Vis Sci. 2017 Jun 1;58(7):2884-2890. doi: 10.1167/iovs.17-21844.
MicroRNAs (miRNAs) are small, endogenous noncoding RNAs that have been detected in human aqueous humor (AH). Prior studies have pooled samples to obtain sufficient quantities for analysis or used next-generation sequencing. Here, we used PCR arrays with preamplification to identify and compare miRNAs from individual AH samples between patients with primary open-angle glaucoma (POAG) and normal controls.
AH was collected before cataract surgery from six stable, medically treated POAG patients and eight age-matched controls. Following reverse transcription and preamplification, individual patient samples were profiled on Taqman Low Density MicroRNA Array Cards. Differentially expressed miRNAs were stratified for fold changes larger than ±2 and for significance of P < 0.05. Significant Kyoto Encyclopedia of Genes and Genomes pathways influenced by the differentially expressed miRNAs were identified using the predicted target module of the miRWalk 2.0 database.
This approach detected 181 discrete miRNAs, which were consistently expressed across all samples of both experimental groups. Significant up-regulation of miR-518d and miR-143, and significant down-regulation of miR-660, was observed in the AH of POAG patients compared with controls. These miRNAs were predicted to reduce cell proliferation and extracellular matrix remodeling, endocytosis, Wnt signaling, ubiquitin-mediated proteolysis, and adherens junction function.
This pilot study demonstrates that miRNA expression within the AH of POAG patients differs from age-matched controls. AH miRNAs exhibit potential as biomarkers of POAG, which merits further investigation in a larger case-controlled study. This technique provides a cost-effective and sensitive approach to assay miRNAs in individual patient samples without the need for pooling.
微小RNA(miRNA)是一类小的内源性非编码RNA,已在人房水(AH)中检测到。先前的研究通过汇集样本以获得足够的量用于分析或使用下一代测序技术。在此,我们使用带有预扩增的PCR阵列来鉴定和比较原发性开角型青光眼(POAG)患者与正常对照个体AH样本中的miRNA。
在白内障手术前从6例病情稳定、接受药物治疗的POAG患者和8例年龄匹配的对照者中收集房水。经过逆转录和预扩增后,在Taqman低密度微小RNA阵列卡上对个体患者样本进行分析。差异表达的miRNA根据大于±2的倍数变化和P<0.05的显著性进行分层。使用miRWalk 2.0数据库的预测靶标模块鉴定受差异表达miRNA影响的重要京都基因与基因组百科全书(KEGG)通路。
该方法检测到181种离散的miRNA,在两个实验组的所有样本中均持续表达。与对照组相比,在POAG患者的房水中观察到miR-518d和miR-143显著上调,miR-660显著下调。预计这些miRNA会减少细胞增殖和细胞外基质重塑、内吞作用、Wnt信号传导、泛素介导的蛋白水解以及黏附连接功能。
这项初步研究表明,POAG患者房水中的miRNA表达与年龄匹配的对照者不同。房水miRNA具有作为POAG生物标志物的潜力,这值得在更大规模的病例对照研究中进一步研究。该技术提供了一种经济高效且灵敏的方法来检测个体患者样本中的miRNA,无需汇集样本。