Department of Human Genetics, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Department of Human Genetics, Faculty of Medicine, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.
Int J Mol Sci. 2021 May 11;22(10):5058. doi: 10.3390/ijms22105058.
(1) Background: Glioblastoma multiforme (GBM) is among the most aggressive cancers with a poor prognosis. Treatment options are limited, clinicians lack efficient prognostic and predictive markers. Circulating miRNAs-besides being important regulators of cancer development-may have potential as diagnostic biomarkers of GBM. (2) Methods: In this study, profiling of 798 human miRNAs was performed on blood plasma samples from 6 healthy individuals and 6 patients with GBM, using a NanoString nCounter Analysis System. To validate our results, five miRNAs (hsa-miR-433-3p, hsa-miR-362-3p, hsa-miR-195-5p, hsa-miR-133a-3p, and hsa-miR-29a-3p) were randomly chosen for RT-qPCR detection. (3) Results: In all, 53 miRNAs were significantly differentially expressed in plasma samples of GBM patients when data were filtered for FC 1 and FDR 0.1. Target genes of the top 39 differentially expressed miRNAs were identified, and we carried out functional annotation and pathway enrichment analysis of target genes via GO and KEGG-based tools. General and cortex-specific protein-protein interaction networks were constructed from the target genes of top miRNAs to assess their functional connections. (4) Conclusions: We demonstrated that plasma microRNA profiles are promising diagnostic and prognostic molecular biomarkers that may find an actual application in the clinical practice of GBM, although more studies are needed to validate our results.
(1) 背景:多形性胶质母细胞瘤(GBM)是预后最差的侵袭性肿瘤之一。治疗方案有限,临床医生缺乏有效的预后和预测标志物。循环 miRNA 除了是癌症发展的重要调节剂外,还有可能成为 GBM 的诊断生物标志物。
(2) 方法:本研究使用 NanoString nCounter 分析系统,对 6 名健康个体和 6 名 GBM 患者的血浆样本进行了 798 个人类 miRNA 的分析。为了验证我们的结果,随机选择了 5 个 miRNA(hsa-miR-433-3p、hsa-miR-362-3p、hsa-miR-195-5p、hsa-miR-133a-3p 和 hsa-miR-29a-3p)进行 RT-qPCR 检测。
(3) 结果:当数据经过 FC 1 和 FDR 0.1 过滤时,所有 53 个 miRNA 在 GBM 患者的血浆样本中均有显著差异表达。鉴定了 top39 个差异表达 miRNA 的靶基因,并通过 GO 和 KEGG 工具对靶基因进行了功能注释和通路富集分析。从 top miRNA 的靶基因构建了通用和皮质特异性蛋白质-蛋白质相互作用网络,以评估它们的功能连接。
(4) 结论:我们证明了血浆 microRNA 谱是有前途的诊断和预后分子生物标志物,可能在 GBM 的临床实践中找到实际应用,尽管还需要更多的研究来验证我们的结果。