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Detection of methylation status of Epstein‐Barr virus DNA C promoter in the diagnosis of nasopharyngeal carcinoma

机译:检测EB病毒DNA C启动子甲基化状态在鼻咽癌诊断中的作用

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摘要

The detection of Epstein‐Barr virus (EBV) DNA load in nasopharyngeal (NP) brushing samples for diagnosis of nasopharyngeal carcinoma (NPC) has attracted great attention. Further improvements that eliminate the need for clinical settings will greatly extend its application. A total of 250 participants were recruited to obtain NP brushing samples. Brush sampling both with and without the guide of endoscopy was conducted in 38 NPC patients. EBV DNA load, EBV RNA transcript and EBV DNA C promoter methylation status were, respectively, evaluated. Typical latency II transcripts were observed in brushing samples from NPC patients but not controls. Unlike in tissues, multiple lytic gene transcripts were observed not only in NPC patients but also in controls. Apart from EBV RNA transcript, samples from NPC patients also showed higher levels of EBV DNA load and C promoter methylation degree than their controls. Qualitative analysis further showed that EBV DNA C promoter was methylated in all NPC patients but in only 18.4% of the control group. Combined analysis of EBV DNA methylated degree and EBV DNA load increased the sensitivity to 100% in the detection of NPC. Using qualitative methylated type as the criteria, up to 89.5% of samples collected via blind brushing showed consistent results with samples collected via endoscopy‐guided brushing from NPC patients. Detection of the methylation status of EBV DNA C promoter in NP brushing samples shows great potential in diagnosing NPC and may provide an appealing alternative for the non–invasive detection and screening of NPC without the need for clinical settings.
机译:在鼻咽(NP)刷洗样本中检测爱泼斯坦-巴尔病毒(EBV)DNA含量以诊断鼻咽癌(NPC)备受关注。无需临床设置的进一步改进将大大扩展其应用范围。总共招募了250名参与者以获得NP刷牙样本。 38例NPC患者在有无内镜检查的情况下均进行了刷式采样。分别评估了EBV DNA载量,EBV RNA转录本和EBV DNA C启动子甲基化状态。在从NPC患者的刷牙样品中观察到典型的潜伏期II转录本,但未在对照组中观察到。与组织不同,不仅在NPC患者中而且在对照中都观察到多种裂解基因转录本。除EBV RNA转录本外,来自NPC患者的样品还显示出比其对照组更高的EBV DNA负载水平和C启动子甲基化程度。定性分析进一步表明,在所有NPC患者中,EBV DNA C启动子均被甲基化,但对照组中只有18.4%。结合分析EBV DNA甲基化程度和EBV DNA载量可将NPC检测的灵敏度提高到100%。以定性甲基化类型为标准,盲刷法收集的样本中多达89.5%与NPC患者通过内窥镜引导刷牙收集的样本具有一致的结果。在NP刷洗样本中检测EBV DNA C启动子的甲基化状态显示出诊断NPC的巨大潜力,并且可能为非侵入性NPC的检测和筛查提供了一种有吸引力的替代方法,而无需临床设置。

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