Shanghai Institute of Pediatric Research, Shanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
Department of Pediatric Neurosurgery, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
ACS Sens. 2022 Aug 26;7(8):2320-2327. doi: 10.1021/acssensors.2c00956. Epub 2022 Aug 4.
The sensitive analysis of microRNAs (miRNAs) in cerebrospinal fluid (CSF) holds promise for the minimally invasive early diagnosis of brain cancers such as pediatric medulloblastoma but remains challenging due partially to a lack of facile yet sensitive sensing methods. Herein, an enzyme-free triple-signal amplification electrochemical assay for miRNA was developed by integrating the target-triggered cyclic strand-displacement reaction (TCSDR), hybridization chain reaction (HCR), and methylene blue (MB) intercalation. In this assay, the presence of target miRNA (miR-9) initiated the TCSDR and produced primers that triggered the subsequent HCR amplification to generate copious double-stranded DNAs (dsDNAs) on the electrode surface. Intercalation of a large number of MB reporters into the long nicked double helixes of dsDNAs yielded a more enhanced signal of differential pulse voltammetry. The enzyme-free multiple-amplification approach allowed for highly sensitive (detection limit: 6.5 fM) and sequence-specific (single-base mismatch resolution) detection of miR-9 from tumor cells and human CSF with minimal sample consumption (10 μL). Moreover, the clinical utilization of this method was documented by accurate discrimination of five medulloblastoma patients from the nontumoral controls. In light of its sensitivity, specificity, and convenience of use, this electrochemical method was expected to facilitate the early detection of malignant brain tumors.
对脑脊液(CSF)中的微小 RNA(miRNAs)进行敏感分析有望实现脑癌(如小儿髓母细胞瘤)的微创早期诊断,但由于缺乏简便而灵敏的传感方法,这一目标仍然具有挑战性。在此,通过整合靶触发循环链置换反应(TCSDR)、杂交链式反应(HCR)和亚甲基蓝(MB)嵌入,开发了一种无酶三重信号扩增电化学测定 miRNA 的方法。在该测定中,靶 miRNA(miR-9)的存在引发了 TCSDR,并产生了引发随后 HCR 扩增的引物,从而在电极表面生成大量双链 DNA(dsDNA)。大量 MB 报告分子嵌入 dsDNA 的长缺口双链中,产生了差分脉冲伏安法的更增强信号。无酶多重扩增方法允许从肿瘤细胞和人 CSF 中高度灵敏(检测限:6.5 fM)和序列特异性(单碱基错配分辨率)检测 miR-9,同时消耗最小的样品量(10 μL)。此外,通过从非肿瘤对照中准确区分五个髓母细胞瘤患者,证明了该方法的临床应用。鉴于其灵敏度、特异性和使用方便性,这种电化学方法有望促进恶性脑肿瘤的早期检测。