Biomedical Engineering Program, North Dakota State University, 1401 Centennial Blvd, Engineering Administration, Room 203, Fargo, North Dakota 58102, United States.
Department of Pharmaceutical Sciences, North Dakota State University, 1401 Albrecht Blvd., Fargo, North Dakota 58102, United States.
Anal Chem. 2023 Jul 11;95(27):10353-10361. doi: 10.1021/acs.analchem.3c01218. Epub 2023 Jun 20.
Pancreatic cancer patients predominantly present with advanced disease at diagnosis, contributing to its high mortality. A noninvasive, fast screening method to detect this disease is an unmet need. Tumor-derived extracellular vesicles (tdEVs) bearing information from parental cells have emerged as a promising cancer diagnostic biomarker. However, most tdEV-based assays have impractical sample volumes and time-consuming, complex, and costly techniques. To overcome these limitations, we developed a novel diagnostic method for pancreatic cancer screening. Our approach utilizes the mitochondrial DNA to nuclear DNA ratio of EVs as a collective cell-specific characteristic. We introduce EvIPqPCR, a fast method that combines immunoprecipitation (IP) and qPCR quantification to detect tumor-derived EVs directly from serum. Importantly, our method employs DNA isolation-free and duplexing probes for qPCR, saving at least 3 h. This technique has the potential to serve as a translational assay for cancer screening with a weak correlation to prognosis biomarkers and sufficient discriminatory power among healthy controls, pancreatitis, and pancreatic cancer cases.
胰腺癌患者在诊断时主要表现为晚期疾病,这导致其死亡率很高。因此,我们需要一种非侵入性、快速的筛查方法来检测这种疾病。携带来自亲代细胞信息的肿瘤衍生细胞外囊泡 (tdEVs) 已成为一种很有前途的癌症诊断生物标志物。然而,大多数基于 tdEV 的检测方法需要不切实际的样本量,且技术耗时、复杂且昂贵。为了克服这些限制,我们开发了一种用于胰腺癌筛查的新型诊断方法。我们的方法利用 EVs 中的线粒体 DNA 与核 DNA 比值作为细胞特异性的集体特征。我们引入了 EvIPqPCR,这是一种快速的方法,它结合了免疫沉淀 (IP) 和 qPCR 定量,可直接从血清中检测肿瘤衍生的 EVs。重要的是,我们的方法采用无 DNA 分离和双链探针进行 qPCR,可节省至少 3 小时。该技术具有作为癌症筛查的转化性检测方法的潜力,与预后生物标志物的相关性较弱,并且在健康对照组、胰腺炎和胰腺癌病例之间具有足够的区分能力。