Yang Hee Cheol, Rhee Won Jong
Department of Bioengineering and Nano-Bioengineering, Incheon National University, Incheon 22012, Korea.
Division of Bioengineering, Incheon National University, Incheon 22012, Korea.
J Clin Med. 2021 Jan 17;10(2):319. doi: 10.3390/jcm10020319.
Because cancers are heterogeneous, it is evident that multiplexed detection is required to achieve disease diagnosis with high accuracy and specificity. Extracellular vesicles (EVs) have been a subject of great interest as sources of novel biomarkers for cancer liquid biopsy. However, EVs are nano-sized particles that are difficult to handle; thus, it is necessary to develop a method that enables efficient and straightforward EV biomarker detection. In the present study, we developed a method for single step in situ detection of EV surface proteins and inner miRNAs simultaneously using a flow cytometer. CD63 antibody and molecular beacon-21 were investigated for multiplexed biomarker detection in normal and cancer EVs. A phospholipid-polymer-phospholipid conjugate was introduced to induce clustering of the EVs analyzed using nanoparticle tracking analysis, which enhanced the detection signals. As a result, the method could detect and distinguish cancer cell-derived EVs using a flow cytometer. Thus, single step in situ detection of multiple EV biomarkers using a flow cytometer can be applied as a simple, labor- and time-saving, non-invasive liquid biopsy for the diagnosis of various diseases, including cancer.
由于癌症具有异质性,显然需要进行多重检测才能实现具有高准确性和特异性的疾病诊断。细胞外囊泡(EVs)作为癌症液体活检新型生物标志物的来源,一直备受关注。然而,EVs是纳米级颗粒,难以处理;因此,有必要开发一种能够实现高效、直接的EV生物标志物检测的方法。在本研究中,我们开发了一种使用流式细胞仪同时原位单步检测EV表面蛋白和内部miRNA的方法。研究了CD63抗体和分子信标-21用于正常和癌症EVs中的多重生物标志物检测。引入磷脂-聚合物-磷脂共轭物以诱导使用纳米颗粒跟踪分析所分析的EVs聚集,从而增强检测信号。结果,该方法可以使用流式细胞仪检测和区分癌细胞衍生的EVs。因此,使用流式细胞仪对多种EV生物标志物进行原位单步检测可作为一种简单、省时省力、非侵入性的液体活检方法,用于诊断包括癌症在内的各种疾病。