Simple Isothermal and Label-Free Strategy for Colorectal Cancer Potential Biomarker miR-625-5p Detection

被引:3
作者
Chen, Yifei [1 ]
Ye, Lizhen [1 ]
Chen, Hui [1 ]
Fan, Tingting [1 ]
Qiu, Cheng [1 ,2 ]
Chen, Yan [2 ]
Jiang, Yuyang [1 ,2 ,3 ]
机构
[1] Tsinghua Shenzhen Int Grad Sch, State Key Lab Chem Oncogen, Guangdong Prov Key Lab Chem Biol, Shenzhen 518055, Peoples R China
[2] Shenzhen Univ, Hlth Sci Ctr, Sch Pharmaceut Sci, Shenzhen 518060, Peoples R China
[3] Tsinghua Univ, Sch Pharmaceut Sci, Beijing 100084, Peoples R China
来源
BIOSENSORS-BASEL | 2023年 / 13卷 / 01期
基金
芬兰科学院;
关键词
colorectal cancer; miR-625-5p; strand displacement amplification; SYBR Gold; MICRORNA; AMPLIFICATION; BIOSENSOR;
D O I
10.3390/bios13010078
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
miRNA is considered a novel biomarker for cancer diagnosis and due to its low level in vivo, the development of new detection methods for it has become a research hotspot in recent years. Here, we firstly found that miR-625-5p was significantly upregulated in colorectal cancer tissues by means of differential expression analysis of the dbDEMC database and clinical validation. Subsequently, it was found that miR-625-5p promoted cell proliferation and migration but inhibited apoptosis through phenotypic experiments; thus, we initially identified miR-625-5p as a potential biomarker for colorectal cancer. Moreover, in order to monitor slight changes in the miR-625-5p level, we developed a novel detection method for it based on strand displacement amplification (SDA). In this system, a hairpin was designed to recognize and pair with miR-625-5p, which was used as a primer to initiate SDA, and a large number of complementary DNAs were generated via cyclic amplification, followed by the addition of SYBR Gold to achieve quantitative analysis of miR-625-5p. Moreover, this method showed a good response to miR-625-5p with a detection limit of 8.6 pM and a dynamic range of 0.01 to 200 nM, and the specificity of it was verified using a set of other miRNAs as an interference. Finally, we set up different concentrations of biologic samples for detection to verify the practicability of the method. The results of this study indicate that this detection method has great potential in clinical diagnosis.
引用
收藏
页数:14
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