Rapid and ultra-sensitive early detection of cervical cancer using CRISPR/ Cas12-based assay based on methylated SEPT9

被引:4
作者
Xu, Wenfei [1 ]
Peng, Jie [3 ]
Guo, Chao [1 ]
Chai, Yingjie [1 ]
Zhou, Haimeng [1 ]
Wang, Jiasi [2 ]
Li, Xuhui [1 ]
机构
[1] Yangtze Delta Reg Inst Tsinghua Univ, Zhejiang Prov Key Lab Appl Enzymol, Zhejiang 314006, Peoples R China
[2] Sun Yat sen Univ, Sch Biomed Engn, Guangdong Prov Key Lab Sensor Technol & Biomed Ins, Shenzhen Campus, Shenzhen 518107, Peoples R China
[3] Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou 310006, Peoples R China
关键词
CRISPR; Cas12a; Methylated SEPT9; MSRE; RPA; Cervical cancer detection; DNA METHYLATION;
D O I
10.1016/j.snb.2022.133231
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cervical cancer is the fourth most common tumor in women with high mortalities. Early diagnosis can improve the survival rate. Nevertheless, there is still a lack of specific biomarkers and efficient methods for the diagnosis of cervical cancer with excellent sensitivity and specificity. In this work, we identified the methylated SEPT9 (mSEPT9) as a specific biomarker for the diagnosis of cervical cancer. We developed a novel method using methylation-sensitive restriction endonuclease (MSRE) combined with recombinase polymerase amplification (RPA)-based CRISPR/Cas12a system (MeCRISPR) for rapid and ultrasensitive detection of mSEPT9. We demonstrated the MeCRISPR enabled to detect 1 copy/mu L of mSEPT9 and distinguishes 0.01% mSEPT9 from large amounts of gDNA. This method could be completed in 60 min without any complicated instruments, which is favorable for point-of-care testing (POCT). We applied MeCRISPR to detect mSEPT9 in clinical cervical cancer patients. The sensitivity and specificity were 100% and 92.3% respectively. Our results demonstrate that mSEPT9 is a promising biomarker for cervical cancer. The MeCRISPR is a sensitive and simple method to analyze the methylated gene which holds great potential for screening cancer in a low-resource setting.
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页数:8
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