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Scanometric microRNA (Scano-miR) Array Profiling of Prostate Cancer Markers Using Spherical Nucleic Acid (SNA)-Gold Nanoparticle Conjugates

机译:scanometric微小RNa(达钺-mIR)使用球形核酸(sNa)-Gold纳米颗粒偶联物前列腺癌标志物的阵列剖面

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摘要

We report the development of a novel Scanometric MicroRNA (Scano-miR) platform for the detection of relatively low abundance miRNAs with high specificity and reproducibility. The Scano-miR system was able to detect 1 fM concentrations of miRNA in serum with single nucleotide mismatch specificity. Indeed, it provides increased sensitivity for miRNA targets compared to molecular fluorophore-based detection systems, where 88% of the low abundance miRNA targets could not be detected under identical conditions. The application of the Scano-miR platform to high density array formats demonstrates its utility for high throughput and multiplexed miRNA profiling from various biological samples. To assess the accuracy of the Scano-miR system, we analyzed the miRNA profiles of samples from victims of prostate cancer (CaP), the most common noncutaneous malignancy and the second leading cause of cancer death among American men. The platform exhibits 98.8% accuracy when detecting deregulated miRNAs involved in CaP, which demonstrates its potential utility in profiling and identifying clinical and research biomarkers.
机译:我们报告了一种新型扫描仪微瘤(Scano-MiR)平台的开发,用于检测具有高特异性和再现性的相对低丰度MIRNA。 Scano-MIR系统能够在血清中检测1 FM浓度的miRNA,具有单一核苷酸不匹配特异性。实际上,与基于分子荧光团的检测系统相比,它为miRNA靶提供了增加的敏感性,其中88%的低丰度miRNA靶不能在相同的条件下检测到。 Scano-MIR平台对高密度阵列格式的应用演示了其用于各种生物样品的高通量和多路复用miRNA分析的实用性。为了评估Scano-miR系统的准确性,我们分析了来自前列腺癌(帽)的受害者的样品的miRNA谱,是美国男性中最常见的非正式恶性肿瘤和癌症死亡的第二个主要原因。当检测概要概念的Derigoged MiRNA时,该平台展示了98.8%的准确性,这证明了其在分析和识别临床和研究生物标志物中的潜在效用。

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