Yang Zhaoqi, Qin Lan, Yang Dutao, Chen Weixia, Qian Yue, Jin Jian
School of Pharmaceutical Sciences, Jiangnan University Wuxi 214122 China
RSC Adv. 2019 Aug 30;9(47):27341-27346. doi: 10.1039/c9ra04663a. eCollection 2019 Aug 29.
Since microRNA-205 (miR-205) is a predictive biomarker for anti-radiation of nasopharyngeal carcinoma (NPC), quantitative detection of miR-205 is important for developing personalized strategies for the treatment of NPC. In this investigation, based on the graphene oxide sensor and duplex specific nuclease (DSN) for fluorescence signal amplification, a highly sensitive detection method for miR-205 was designed. A target-recycling mechanism is employed, where a single miR-205 target triggers the cleavage of many DNA signal probes. The method shows the ability to analyze miR-205 in solution, and it can detect miR-205 at concentrations as low as 132 pmol L with a linear range of 5-40 nmol L. Furthermore, the method is specific in that it distinguishes between a target miRNA and a sequence with single base, double base and three base mismatches, as well as other miRNAs. Considering simplicity and excellent sensitivity/specificity, it is promising for applications in radioresistance studies as well as the early clinical diagnosis of NPC.
由于微小RNA-205(miR-205)是鼻咽癌(NPC)抗辐射的预测生物标志物,因此miR-205的定量检测对于制定NPC个性化治疗策略至关重要。在本研究中,基于氧化石墨烯传感器和用于荧光信号放大的双链特异性核酸酶(DSN),设计了一种高灵敏度的miR-205检测方法。采用了靶循环机制,其中单个miR-205靶标触发许多DNA信号探针的切割。该方法能够分析溶液中的miR-205,其线性范围为5-40 nmol/L,能够检测低至132 pmol/L浓度的miR-205。此外,该方法具有特异性,能够区分靶标微小RNA与具有单碱基、双碱基和三碱基错配的序列以及其他微小RNA。考虑到其简便性和出色的灵敏度/特异性,该方法在放射抗性研究以及NPC的早期临床诊断中具有应用前景。