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开发并验证一种新型基于鼻咽拭子的 Epstein-Barr 病毒 C 启动子甲基化定量检测方法,用于鼻咽癌的检测。

Development and analytical validation of a novel nasopharynx swab-based Epstein-Barr virus C promoter methylation quantitative assay for nasopharyngeal carcinoma detection.

机构信息

Department of Cancer Prevention, Sun Yat-sen University Cancer Center, Guangzhou, P.R. China.

State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-sen University Cancer Center, Guangzhou, P.R. China.

出版信息

Clin Chem Lab Med. 2023 Aug 4;62(1):187-198. doi: 10.1515/cclm-2023-0510. Print 2024 Jan 26.

DOI:10.1515/cclm-2023-0510
PMID:37531579
Abstract

OBJECTIVES

Epstein-Barr virus (EBV) C promoter (Cp) hypermethylation, a crucial factor for EBV latent infection of nasopharyngeal epithelial cells, has been recognized as a promising biomarker for nasopharyngeal carcinoma (NPC) detection. In this study, we develop a novel EBV Cp methylation quantification (E-CpMQ) assay and evaluate its diagnostic performance for NPC detection.

METHODS

A novel qPCR assay for simultaneous quantification of methylated- and unmethylated EBV Cp was developed by the combinational modification of MethyLight and QASM, with an innovative calibrator to improve the detection accuracy and consistency. The NP swab samples and synthetic standards were used for the analytical validation of the E-CpMQ. The diagnostic efficacy of the developed E-CpMQ assay was validated in 137 NPC patients and 137 non-NPC controls.

RESULTS

The E-CpMQ assay can detect the EBV Cp methylation ratio in one reaction system under 10 copies with 100 % recognition specificity, which is highly correlated to pyrosequencing with a correlation coefficient over 0.99. The calibrated E-CpMQ assay reduces the coefficient of variation by an average of 55.5 % with a total variance of less than 0.06 units standard deviation (SD). Linear methylation ratio detection range from 4.76 to 99.01 %. The sensitivity and specificity of the E-CpMQ respectively are 96.4 % (95 % CI: 91.7-98.8 %), 89.8 % (95 % CI: 83.5-94.3 %).

CONCLUSIONS

The developed E-CpMQ assay with a calibrator enables accurate and reproducible EBV Cp methylation ratio quantification and offers a sensitive, specific, cost-effective method for NPC early detection.

摘要

目的

Epstein-Barr 病毒(EBV)C 启动子(Cp)超甲基化是 EBV 潜伏感染鼻咽上皮细胞的关键因素,已被认为是鼻咽癌(NPC)检测的有前途的生物标志物。在本研究中,我们开发了一种新型 EBV Cp 甲基化定量(E-CpMQ)检测方法,并评估了其用于 NPC 检测的诊断性能。

方法

通过对 MethyLight 和 QASM 的联合修饰,开发了一种用于同时定量甲基化和未甲基化 EBV Cp 的新型 qPCR 检测方法,并采用创新的校准品来提高检测的准确性和一致性。NP 拭子样本和合成标准品用于 E-CpMQ 的分析验证。对 137 名 NPC 患者和 137 名非 NPC 对照组的开发的 E-CpMQ 检测方法的诊断效果进行了验证。

结果

E-CpMQ 检测方法在 10 拷贝以下的一个反应体系中可检测到 EBV Cp 甲基化比率,具有 100%的识别特异性,与焦磷酸测序高度相关,相关系数超过 0.99。校准后的 E-CpMQ 检测方法平均降低了 55.5%的变异系数,总方差小于 0.06 个标准差(SD)。线性甲基化比率检测范围为 4.76 至 99.01%。E-CpMQ 的灵敏度和特异性分别为 96.4%(95%CI:91.7-98.8%)和 89.8%(95%CI:83.5-94.3%)。

结论

该研究开发的具有校准品的 E-CpMQ 检测方法能够准确、可重复地定量 EBV Cp 甲基化比率,为 NPC 的早期检测提供了一种敏感、特异、经济有效的方法。

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