Zhuang Jianjian, Jiang Hong, Lou Jiang, Zhang Yu
Department of Clinical pharmacology, Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province, Affiliated Hangzhou First People's Hospital, Cancer Center, Westlake University School of Medicine, Hangzhou, Zhejiang, 310006, China.
Department of Clinical pharmacology, Affiliated Hangzhou First People's Hospital, Cancer Center, Westlake University School of Medicine, Hangzhou, Zhejiang, 310006, China.
Talanta. 2025 Feb 1;283:127162. doi: 10.1016/j.talanta.2024.127162. Epub 2024 Nov 6.
Epidermal Growth Factor Receptor (EGFR) is an important target for the early evaluation, treatment, and postoperative follow-up in non-small cell lung cancer (NSCLC). Current detection technologies suffer from extended detection time and high rate of false positive amplification. Therefore, the development of rapid, highly sensitive and specific detection methods is of great significance for improving the diagnosis and treatment of lung cancer. In this study, we proposed a fast and sensitive detection method termed Thermus thermophilus Argonaute (Ttago)-Coupled-Multiplex-digital-recombinase polymerase amplification (RPA)-Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas12a (TCMDC) detection method, integrating EGFR mutation template enrichment. Based on the cleavage principle of TtAgo, the wild type (WT) template was enriched under the action of double-guide DNA. Two CRISPR RNAs, not restricted by protospacer adjacent motif (PAM) sites, were introduced to target EGFR genes. By combining RPA with CRISPR-Cas12a, we established a single-pot, ultra-sensitive (1 copy, 0.1 %), and visually detectable method for EGFR detection. We further verified the feasibility of this approach using clinical serum samples from lung cancer patients, achieving rapid (within 1 h) and visual detection of EGFR, thereby presenting a promising clinical tool for the detection of lung cancer.
表皮生长因子受体(EGFR)是非小细胞肺癌(NSCLC)早期评估、治疗及术后随访的重要靶点。目前的检测技术存在检测时间长和假阳性扩增率高的问题。因此,开发快速、高灵敏且特异的检测方法对改善肺癌的诊断和治疗具有重要意义。在本研究中,我们提出了一种快速灵敏的检测方法,即嗜热栖热菌Argonaute(TtAgo)偶联多重数字重组酶聚合酶扩增(RPA)-成簇规律间隔短回文重复序列(CRISPR)/Cas12a(TCMDC)检测方法,并整合了EGFR突变模板富集。基于TtAgo的切割原理,野生型(WT)模板在双引导DNA作用下得以富集。引入两条不受原间隔序列临近基序(PAM)位点限制的CRISPR RNA靶向EGFR基因。通过将RPA与CRISPR-Cas12a相结合,我们建立了一种单管、超灵敏(1拷贝,0.1%)且可视觉检测的EGFR检测方法。我们进一步使用肺癌患者的临床血清样本验证了该方法的可行性,实现了EGFR的快速(1小时内)且可视化检测,从而为肺癌检测提供了一种有前景的临床工具。