利用基于肽核酸的微阵列分析胶质细胞肿瘤中微小RNA的表达

IF 1.9 Q2 MEDICINE, GENERAL & INTERNAL
Dae Cheol Kim, Young Zoon Kim
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引用次数: 1

摘要

目的:胶质瘤是最常见的原发性脑肿瘤。然而,它们的特征和预后很难辨别。目前重点是微小RNA(miRNA)作为神经胶质瘤的候选生物标志物。本研究的目的是通过在各种神经胶质肿瘤和正常组织样本中使用基于肽核酸(PNA)的微阵列来鉴定神经胶质肿瘤中的特异性miRNA模式。方法:对两个研究所病理档案中诊断为神经胶质瘤的病例的样本文件进行回顾性评估。应用微阵列技术对28例胶质细胞肿瘤的miRNA进行分析。为了验证结果,进行了定量实时聚合酶链式反应(RT-PCR)。使用2方法计算miRNA的表达。使用SPSS 20.0版(IBM Co.)比较miRNA的表达水平。结果:神经胶质瘤的miRNA表达谱显示,在胶质母细胞瘤和良性脑组织中检测到62个miRNA,具有不同的表达模式。miR-296-3p、miR-370和miR-371-5p的表达显示与恶性肿瘤有关。这些miRNA在使用甲基化O6甲基胍DNA甲基转移酶的胶质母细胞瘤中也增加。miR-296-3p的表达模式在基于PNA的微阵列和RT-PCR中显示出相同的趋势。结论:这些分析表明,新的miRNA可以作为诊断工具和靶向治疗剂,因为miRNA可以正向或负向调节胶质母细胞瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of microRNA expression in glial tumors by using a peptide nucleic acid-based microarray
Purpose: Glial tumors are the most common primary brain tumors. However, their characteristics and prognosis are difficult to discern. There is currently an emphasis on microRNAs (miRNA) as candidate biomarkers for glial tumors. The aim of this study is to identify the specific miRNA patterns in glial tumors by using peptide nucleic acid (PNA)based microarrays in an assortment of glial tumors and normal tissue samples. Methods: Sample files were retrospectively assessed for cases diagnosed as glial tumors at the pathological archives of two institutes. miRNAs of 28 cases of glial tumors were analyzed by microarray. In order to verify the results, quantitative real-time polymerase chain reaction (RT-PCR) was performed. miRNA expression was calculated using the 2 method. The expression level of the miRNAs was compared using SPSS version 20.0 (IBM Co.). Results: miRNA expression profiling of glial tumors revealed that 62 miRNAs were detected from glioblastoma and benign brain tissue, with different expression patterns. The expression of miR-296-3p, miR-370, and miR-371-5p was shown to be involved in malignancy. These miRNAs were also increased in the glioblastoma with methylated O6-methyguanine DNA methyltransferase. The expression pattern of miR-296-3p shows same tendency in PNA-based microarray and RT-PCR. Conclusion: These analyses suggest that novel miRNAs can be applicable as diagnostic tools and target therapeutic agents, since miRNAs can positively or negatively regulate glioblastomas.
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来源期刊
Precision and Future Medicine
Precision and Future Medicine MEDICINE, GENERAL & INTERNAL-
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