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PAX1的DNA甲基化作为口腔鳞状细胞癌的生物标志物

DNA methylation of PAX1 as a biomarker for oral squamous cell carcinoma.

作者信息

Huang Yung-Kai, Peng Bou-Yu, Wu Chia-Yo, Su Chien-Tien, Wang Hui-Chen, Lai Hung-Cheng

机构信息

School of Oral Hygiene, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.

出版信息

Clin Oral Investig. 2014 Apr;18(3):801-8. doi: 10.1007/s00784-013-1048-6. Epub 2013 Aug 2.

Abstract

OBJECTIVES

DNA methylation has been shown to be a promising cancer biomarker. The aim of this study was to evaluate DNA methylation of three transcription factors, sex-determining region Y-box 1 (SOX1), paired box gene 1 (PAX1), and zinc-finger 582 (ZNF582), in detecting oral squamous cell carcinoma (OSCC).

MATERIALS AND METHODS

A case-control study was conducted at Taipei Medical University Hospital in Taiwan with 31 cases of various oral cavity squamous cell carcinomas and 40 controls. Questionnaire data assessing environmental exposure, such as alcohol consumption, cigarette smoking, and betel nut chewing, were obtained from each participant. DNA from oral swabs were analyzed for methylation using quantitative methylation polymerase chain reaction with TaqMan probes. Methylation status was determined using a methylation index.

RESULTS

Methylation levels of SOX1, PAX1, and ZNF582 were significantly higher in cancer patients (p = 0.02, p = 0.02, and p = 0.03, respectively). Patients with highly methylated SOX1, PAX1, and ZNF582 had an increased cancer risk with odds ratios (ORs) of 16.50 (95 % CI = 2.85-96.65), 60.57 (95 % CI = 5.85-629.94), and 5.07 (95 % CI = 1.08-23.76), respectively. Area under the curve (AUC) values were 0.85, 0.78, and 0.78 for PAX1, SOX1, and ZNF582, respectively. When stratified based on environmental exposure, the AUC of PAX1 methylation (PAX1 (m) ) was 0.94 in environmental exposure-naïve subjects and 0.85 for SOX1 methylation in subjects who chewed betel nut. In general, the sensitivity and specificity of PAX1 (m) were 87 and 80 % for OSCC detection. The sensitivity of PAX1 (m) in subjects who chewed betel nut was 83 %, with a specificity of 75 %.

CONCLUSIONS

Testing PAX1 DNA methylation using oral swabs is a promising method for oral cancer detection. Combined assessments regarding betel nut consumption and DNA methylation can improve OSCC screening.

CLINICAL RELEVANCE

The double E (environmental and epigenetic) assessment is a potential strategy in OSCC screening.

摘要

目的

DNA甲基化已被证明是一种很有前景的癌症生物标志物。本研究的目的是评估三种转录因子,即性别决定区Y盒1(SOX1)、配对盒基因1(PAX1)和锌指蛋白582(ZNF582)的DNA甲基化在检测口腔鳞状细胞癌(OSCC)中的作用。

材料与方法

在台湾台北医学大学医院进行了一项病例对照研究,纳入31例各种口腔鳞状细胞癌患者和40名对照者。从每位参与者处获取评估环境暴露情况的问卷数据,如饮酒、吸烟和嚼槟榔情况。使用带有TaqMan探针的定量甲基化聚合酶链反应分析口腔拭子中的DNA甲基化情况。使用甲基化指数确定甲基化状态。

结果

癌症患者中SOX1、PAX1和ZNF582的甲基化水平显著更高(分别为p = 0.02、p = 0.02和p = 0.03)。SOX1、PAX1和ZNF582高度甲基化的患者癌症风险增加,优势比(OR)分别为16.50(95%可信区间[CI]=2.85 - 96.65)、60.57(95%CI = 5.85 - 629.94)和5.07(95%CI = 1.08 - 23.76)。PAX1、SOX1和ZNF582的曲线下面积(AUC)值分别为0.85、0.78和0.78。根据环境暴露情况分层时,在未暴露于环境因素的受试者中,PAX1甲基化(PAX1(m))的AUC为0.94,在嚼槟榔的受试者中,SOX1甲基化的AUC为0.85。总体而言,PAX1(m)检测OSCC的敏感性和特异性分别为87%和80%。PAX1(m)在嚼槟榔受试者中的敏感性为83%,特异性为75%。

结论

使用口腔拭子检测PAX1 DNA甲基化是一种很有前景的口腔癌检测方法。结合嚼槟榔情况和DNA甲基化的评估可以改善OSCC筛查。

临床意义

双E(环境和表观遗传)评估是OSCC筛查的一种潜在策略。

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