Department of General Surgery , Huashan Hospital, Fudan University , Shanghai , 200040 China.
Department of Medicine , Roswell Park Comprehensive Cancer Center , Buffalo , New York 14263 , United States.
ACS Sens. 2018 Aug 24;3(8):1471-1479. doi: 10.1021/acssensors.8b00230. Epub 2018 Jul 31.
Exosomes are small extracellular vesicles released by cells for cell-cell communication. They play important roles in cancer development, metastasis, and drug resistance. Exosomal proteins have been demonstrated by many studies as promising biomarkers for cancer screening, diagnosis, and monitoring. Among many detection techniques, surface plasmon resonance (SPR) is a highly sensitive, label-free, and real-time optical detection method. Commercial prism-based wavelength/angular-modulated SPR sensors afford high sensitivity and resolution, but their large footprint and high cost limit their adaptability for clinical settings. Recently, a nanoplasmonic exosome (nPLEX) assay was developed to detect exosomal proteins for ovarian cancer diagnosis. However, comparing with conventional SPR biosensors, the broad applications of nanoplasmonic biosensors are limited by the difficult and expensive fabrication of nanostructures. We have developed an intensity-modulated, compact SPR biosensor (25 cm × 10 cm × 25 cm) which uses a conventional SPR sensing mechanism and does not require nanostructure fabrication. Calibration from glycerol showed that the compact SPR biosensor offered sensitivity of 9.258 × 10%/RIU and resolution of 8.311 × 10 RIU. We have demonstrated the feasibility of the compact SPR biosensor in lung cancer diagnosis using exosomal epidermal growth factor receptor (EGFR) and programmed death-ligand 1 (PD-L1) as biomarkers. It detected a higher level of exosomal EGFR from A549 nonsmall cell lung cancer (NSCLC) cells than BEAS-2B normal cells. With human serum samples, the compact SPR biosensor detected similar levels of exosomal EGFR in NSCLC patients and normal controls, and higher expression of exosomal PD-L1 in NSCLC patients than normal controls. The compact SPR biosensor showed higher detection sensitivity than ELISA and similar sensing accuracy as ELISA. It is a simple and user-friendly sensing platform, which may serve as an in vitro diagnostic test for cancer.
外泌体是细胞释放的用于细胞间通讯的小细胞外囊泡。它们在癌症发展、转移和耐药性中发挥重要作用。许多研究表明,外泌体蛋白是癌症筛查、诊断和监测的有前途的生物标志物。在许多检测技术中,表面等离子体共振(SPR)是一种高灵敏度、无标记和实时的光学检测方法。商用棱镜式波长/角度调制 SPR 传感器具有高灵敏度和分辨率,但它们的大尺寸和高成本限制了它们在临床环境中的适应性。最近,开发了一种纳米等离子体外泌体(nPLEX)检测法来检测外泌体蛋白以进行卵巢癌诊断。然而,与传统的 SPR 生物传感器相比,纳米等离子体生物传感器的广泛应用受到制造纳米结构的困难和昂贵的限制。我们开发了一种强度调制、紧凑的 SPR 生物传感器(25cm×10cm×25cm),该传感器使用传统的 SPR 传感机制,不需要制造纳米结构。从甘油的校准结果表明,紧凑的 SPR 生物传感器提供了 9.258×10%/RIU 的灵敏度和 8.311×10 RIU 的分辨率。我们已经证明了紧凑的 SPR 生物传感器在使用外泌体表皮生长因子受体(EGFR)和程序性死亡配体 1(PD-L1)作为生物标志物进行肺癌诊断中的可行性。它从 A549 非小细胞肺癌(NSCLC)细胞中检测到比 BEAS-2B 正常细胞更高水平的外泌体 EGFR。用人血清样本,紧凑的 SPR 生物传感器在 NSCLC 患者和正常对照组中检测到类似水平的外泌体 EGFR,并在 NSCLC 患者中检测到更高水平的外泌体 PD-L1。紧凑的 SPR 生物传感器的检测灵敏度高于 ELISA,与 ELISA 的传感准确性相当。它是一种简单易用的传感平台,可作为癌症的体外诊断测试。