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An exploration of nucleic acid liquid biopsy using a glucose meter

机译:使用血糖仪进行核酸液体活检的探索

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摘要

The development of non-invasive techniques for the diagnosis of cancer, characterization of mutation and monitoring treatment response could greatly reduce the morbidity and mortality caused by cancer. Nevertheless, the extremely low amount of cell free nucleic acids makes liquid biopsy a very challenging task. Herein, taking advantage of the pocket size, reliable quantitative results and simple operation of the pocket-sized personal glucose meter (PGM), we report an approach of circulating microRNA-21 (miR-21) detection with high precision and low cost. Via target-induced release of invertase from the DNA–invertase conjugate, which could convert sucrose into glucose, the detection of miR-21 in serum was linked to PGM readings. Combining the DNAzyme feedback amplification (DFA) program and highly efficient enzymatic turnover, an ultralow detection limit of 7 × 10–16 M for miR-21 was achieved using a PGM as the reporter. The high sensitivity and selectivity of the proposed method meets the requirement of quantifying cell free nucleic acids in serum. In addition, this approach fills the shortage of quantitative RT-PCR and next-generation sequencing in quantifying miRNAs with a short length and greatly reduces the cost of detection. We believe that widely used personal diagnosis devices could hold an important place in the booming area of liquid biopsy.
机译:用于癌症诊断,突变表征和监测治疗反应的非侵入性技术的发展可以大大降低癌症引起的发病率和死亡率。然而,极少的无细胞核酸数量使液体活检成为一项非常艰巨的任务。本文中,我们利用袖珍型个人血糖仪(PGM)的袖珍大小,可靠的定量结果和简单操作的优势,报告了一种以高精度和低成本进行循环microRNA-21(miR-21)检测的方法。通过靶标诱导的可从蔗糖转化为葡萄糖的DNA-蔗糖酶结合物中蔗糖酶的释放,血清中miR-21的检测与PGM读数相关。结合DNAzyme反馈扩增(DFA)程序和高效的酶转化,使用PGM作为报告基因,miR-21的检测限达到了7×10 –16 M的超低水平。所提方法的高灵敏度和选择性满足定量血清中无细胞核酸的要求。另外,这种方法填补了定量RT-PCR和下一代测序在短长度miRNA定量方面的不足,并大大降低了检测成本。我们相信,广泛使用的个人诊断设备可以在液体活检蓬勃发展的领域中占有重要地位。

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