State Key Laboratory of Oncogenes and Related Genes, Institute for Personalized Medicine, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, 200030, China.
Institute of Nano Biomedicine and Engineering, Shanghai Engineering Research Centre for Intelligent Diagnosis and Treatment Instrument, Department of Instrument Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
J Nanobiotechnology. 2021 Sep 26;19(1):287. doi: 10.1186/s12951-021-01039-4.
Pancreatic cancer, at unresectable advanced stages, presents poor prognoses, which could be prevented by early pancreatic cancer diagnosis methods. Recently, a promising early-stage pancreatic cancer biomarker, extracellular vesicles (EVs) related glypican-1 (GPC1) mRNA, is found to overexpress in pancreatic cancer cells. Current mRNA detection methods usually require expensive machinery, strict preservation environments, and time-consuming processes to guarantee detection sensitivity, specificity, and stability. Herein, we propose a novel two-step amplification method (CHAGE) via the target triggered Catalytic Hairpin Assembly strategy combined with Gold-Enhanced point-of-care-testing (POCT) technology for sensitive visual detection of pancreatic cancer biomarker. First, utilizing the catalyzed hairpin DNA circuit, low expression of the GPC1 mRNA was changed into amplification product 1 (AP1, a DNA duplex) as the next detection targets of the paper strips. Second, the AP1 was loaded onto a lateral flow assay and captured with the gold signal nanoparticles to visualize results. Finally, the detected results can be further enhanced by depositing gold to re-enlarge the sizes of gold nanoparticles in detection zones. As a result, the CHAGE methodology lowers the detection limit of mRNA to 100 fM and provides results within 2 h at 37 °C. Furthermore, we demonstrate the successful application in discriminating pancreatic cancer cells by analyzing EVs' GPC1 mRNA expression levels. Hence, the CHAGE methodology proposed here provides a rapid and convenient POCT platform for sensitive detection of mRNAs through unique probes designs (COVID, HPV, etc.).
在不可切除的晚期阶段,胰腺癌预后较差,通过早期胰腺癌诊断方法可以预防。最近,一种有前途的早期胰腺癌生物标志物,细胞外囊泡(EVs)相关的磷脂酰聚糖-1(GPC1)mRNA,被发现过度表达于胰腺癌细胞中。目前的 mRNA 检测方法通常需要昂贵的仪器、严格的保存环境和耗时的过程,以保证检测的灵敏度、特异性和稳定性。在此,我们提出了一种新的两步放大方法(CHAGE),通过目标触发的催化发夹组装策略与金增强即时检测(POCT)技术相结合,用于敏感可视化检测胰腺癌生物标志物。首先,利用催化发夹 DNA 电路,将 GPC1 mRNA 的低表达转化为扩增产物 1(AP1,一种 DNA 双链),作为纸条的下一个检测目标。其次,AP1 加载到侧流分析中,并与金信号纳米颗粒结合以可视化结果。最后,通过沉积金来重新放大检测区域中的金纳米颗粒的尺寸,进一步增强检测结果。结果表明,CHAGE 方法将 mRNA 的检测下限降低到 100 fM,并在 37°C 下 2 小时内提供结果。此外,我们通过分析 EVs 的 GPC1 mRNA 表达水平,成功地应用于区分胰腺癌细胞。因此,这里提出的 CHAGE 方法通过独特的探针设计(COVID、HPV 等),为敏感检测 mRNA 提供了一种快速方便的 POCT 平台。