Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina.
Center for Oral/Head & Neck Oncology Research, School of Dentistry, University of California Los Angeles, Los Angeles, California.
J Mol Diagn. 2020 Jan;22(1):50-59. doi: 10.1016/j.jmoldx.2019.08.004.
Previous efforts to evaluate the detection of human papilloma viral (HPV) DNA in whole saliva as a diagnostic measure for HPV-associated oropharyngeal cancer (HPV-OPC) have not shown sufficient clinical performance. We hypothesize that salivary exosomes are packaged with HPV-associated biomarkers, and efficient enrichment of salivary exosomes through isolation can enhance diagnostic and prognostic performance for HPV-OPC. In this study, an acoustofluidic (the fusion of acoustics and microfluidics) platform was developed to perform size-based isolation of salivary exosomes. These data showed that this platform is capable of consistently isolating exosomes from saliva samples, regardless of viscosity variation and collection method. Compared with the current gold standard, differential centrifugation, droplet digital RT-PCR analysis showed that the average yield of salivary exosomal small RNA from the acoustofluidic platform is 15 times higher. With this high-yield exosome isolation platform, we show that HPV16 DNA could be detected in isolated exosomes from the saliva of HPV-associated OPC patients at 80% concordance with tissues/biopsies positive for HPV16. Overall, these data demonstrated that the acoustofluidic platform can achieve high-purity and high-yield salivary exosome isolation for downstream salivary exosome-based liquid biopsy applications. Additionally, HPV16 DNA sequences in HPV-OPC patients are packaged in salivary exosomes and their isolation will enhance the detection of HPV16 DNA.
先前评估全唾液中人乳头瘤病毒 (HPV) DNA 作为 HPV 相关口咽癌 (HPV-OPC) 诊断指标的努力并未显示出足够的临床性能。我们假设唾液外泌体包裹着 HPV 相关的生物标志物,通过分离有效地富集唾液外泌体可以提高 HPV-OPC 的诊断和预后性能。在这项研究中,开发了一种声流(声学和微流控的融合)平台来进行基于大小的唾液外泌体分离。这些数据表明,该平台能够始终如一地从唾液样本中分离出外泌体,无论粘度变化和采集方法如何。与目前的金标准相比,微滴数字 RT-PCR 分析显示,声流平台分离的唾液外泌体小 RNA 的平均产量高 15 倍。利用这个高产量的外泌体分离平台,我们发现 HPV16 DNA 可以在与 HPV16 阳性的组织/活检相吻合的 HPV 相关 OPC 患者的唾液中分离出的外泌体中以 80%的一致性检测到。总的来说,这些数据表明声流平台可以实现高纯度和高产量的唾液外泌体分离,用于下游基于唾液外泌体的液体活检应用。此外,HPV-OPC 患者的 HPV16 DNA 序列被包装在唾液外泌体中,其分离将增强 HPV16 DNA 的检测。