| Literature DB >> 29486117 |
Xin-Yuan Qiu1, Lv-Yun Zhu1, Chu-Shu Zhu1, Jia-Xin Ma1, Tao Hou2, Xiao-Min Wu1, Si-Si Xie1, Lu Min1, De-An Tan3, Dong-Yi Zhang1, Lingyun Zhu1.
Abstract
MicroRNAs have been reported as related to multiple diseases and have potential applications in diagnosis and therapeutics. However, detection of miRNAs remains improvable, given their complexity, high cost, and low sensitivity as of currently. In this study, we attempt to build a novel platform that detects miRNAs at low cost and high efficacy. This detection system contains isothermal amplification, detecting and reporting process based on rolling circle amplification, CRISPR-Cas9, and split-horseradish peroxidase techniques. It is able to detect trace amount of miRNAs from samples with mere single-base specificity. Moreover, we demonstrated that such scheme can effectively detect target miRNAs in clinical serum samples and significantly distinguish patients of non-small cell lung cancer from healthy volunteers by detecting the previously reported biomarker: circulating let-7a. As the first to use CRISPR-Cas9 in miRNA detection, this method is a promising approach capable of being applied in screening, diagnosing, and prognosticating of multiple diseases.Entities:
Keywords: CRISPR-dCas9; biomarker; miRNA detection; rolling circle amplification; split reporter
Mesh:
Substances:
Year: 2018 PMID: 29486117 DOI: 10.1021/acssynbio.7b00446
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110