Dumbbell probe initiated multi-rolling circle amplification assisted CRISPR/Cas12a for highly sensitive detection of clinical microRNA

被引:2
|
作者
Shen, Xudan [1 ]
Lin, Ziwei [1 ]
Jiang, Xianfeng [1 ]
Zhu, Xinlan [1 ]
Zeng, Su [1 ]
Cai, Sheng [1 ,2 ]
Liu, Hui [1 ]
机构
[1] Zhejiang Univ, Sir Run Run Shaw Hosp, Coll Pharmaceut Sci, Clin Res Ctr,Sch Med, Hangzhou 310020, Zhejiang, Peoples R China
[2] Zhejiang Univ, Jinhua Inst, Jinhua 321299, Zhejiang, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
microRNA; Rolling circle amplification; CRISPR/Cas12a; Clinical sample; NUCLEIC-ACID DETECTION; MESENCHYMAL TRANSITION;
D O I
10.1016/j.bios.2024.116676
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel miRNA detection technique named Dumbbell probe initiated multi-Rolling Circle Amplification assisted CRISPR/Cas12a (DBmRCA) was developed relying on the ligation-free dumbbell probe and the high-sensitivity CRISPR/Cas12a signal out strategy. This DBmRCA assay streamlines miRNA quantification within a mere 30-min timeframe and with exceptional analytical precision. The efficacy of this method was validated by assessing miRNA levels in clinical samples, revealing distinct expression panel of miR-200a and miR-126 in lung cancer/ adjacent/normal tissue specimens. Moreover, a predictive model was established to classify benign and malignant tumor. Due to its time efficiency, enhanced sensitivity, and streamlined workflow, this assay would be a reliable tool for miRNA analysis in clinical settings, offering potential guidance for early diagnosis and treatment of lung cancer.
引用
收藏
页数:7
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