Isothermal circular strand displacement-based assay for microRNA detection in liquid biopsy

被引:7
|
作者
Bellassai, Noemi [1 ]
D'Agata, Roberta [1 ]
Spoto, Giuseppe [1 ,2 ]
机构
[1] Univ Catania, Dipartimento Sci Chim, Viale Andrea Doria 6, I-95125 Catania, Italy
[2] Univ Catania, Consorzio Interuniv Ist Nazl Biostrutture & Biosi, Dipartimento Sci Chim, Viale Andrea Doria 6, Catania, Italy
关键词
MicroRNA; Liquid biopsy; Isothermal amplification; Nucleic acid amplification; Microfluidic devices; Osteoarthritis; LUNG-CANCER; ULTRASENSITIVE DETECTION; NUCLEIC-ACID; OSTEOARTHRITIS; AMPLIFICATION; MIRNA; BIOMARKERS; PROBES; KNEE; DNA;
D O I
10.1007/s00216-022-04228-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Extracellular miRNAs are promising targets for developing new assays for the early diagnosis and prognosis of diseases based on liquid biopsy. The detection of miRNAs in liquid biopsies is challenged by their short sequence length, low concentration, and interferences with bodily fluid components. Isothermal circular strand displacement polymerization has emerged as a convenient method for nucleic acid amplification and detection. Herein, we describe an innovative strategy for microRNA detection directly from biological fluids based on hairpin probe-assisted isothermal amplification reaction. We designed and optimized the assay to detect target analytes in 1 mu L of the complex media's biological matrix using a microfluidic device for the straightforward analysis of multiple samples. We validated the assay to detect circulating miR-127-5p in synovial fluid, recently indicated as a predictive biomarker for osteoarthritis disease. The combined use of a mutant polymerase operating with high yield and a primer incorporating locked nucleic acid nucleosides allowed detection of miR-127-5p with 34 fmol L-1 LOD. We quantified circulating miR-127-5p directly in synovial fluid, thus demonstrating that the assay may be employed for the convenient detection of 4.3 +/- 0.5 pmol L-1 concentrated miRNAs in liquid biopsy samples.
引用
收藏
页码:6431 / 6440
页数:10
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