Detection of miRNAs with a nanopore single-molecule counter

被引:0
|
作者
Gu, Li-Qun [1 ]
Wanunu, Meni [2 ]
Wang, Michael X. [3 ]
McReynolds, Larry [4 ]
Wang, Yong [1 ]
机构
[1] Univ Missouri, Dalton Cardiovasc Res Ctr, Columbia, MO 65211 USA
[2] Northeastern Univ, Dept Phys & Chem Chem Biol, Nanoscale Biophys Lab, Boston, MA 02115 USA
[3] Univ Missouri, Dept Pathol & Anat Sci, Ellis Fischel Canc Ctr, Columbia, MO 65203 USA
[4] New England Biolabs Inc, Div RNA Biol, Ipswich, MA 01938 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
biomarker; biosensor; diagnostics; lung cancer; miRNA; nanopore; noninvasive detection; PCR; IN-SITU DETECTION; MICRORNA EXPRESSION PROFILES; SEQUENCE-SPECIFIC DETECTION; INDIVIDUAL DNA STRANDS; FORMALIN-FIXED TISSUES; CELL LUNG-CANCER; ALPHA-HEMOLYSIN; ORIENTATION DISCRIMINATION; CIRCULATING MICRORNAS; SMALL RNAS;
D O I
10.1586/ERM.12.58
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
miRNAs are short noncoding RNA molecules that are important in regulating gene expression. Due to the correlation of their expression levels and various diseases, miRNAs are being investigated as potential biomarkers for molecular diagnostics. The fast-growing miRNA exploration demands rapid, accurate, low-cost miRNA detection technologies. This article will focus on two platforms of nanopore single-molecule approach that can quantitatively measure miRNA levels in samples from tissue and cancer patient plasma. Both nanopore methods are sensitive and specific, and do not need labeling, enzymatic reaction or amplification. In the next 5 years, the nanopore-based miRNA techniques will be improved and validated for noninvasive and early diagnosis of diseases.
引用
收藏
页码:573 / 584
页数:12
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