Hall Gillian L, Shaw Richard J, Field E Anne, Rogers Simon N, Sutton David N, Woolgar Julia A, Lowe Derek, Liloglou Triantafillos, Field John K, Risk Janet M
Molecular Genetics and Oncology Group, Department of Clinical Dental Sciences, University of Liverpool, Liverpool L69 3GN, United Kingdom.
Cancer Epidemiol Biomarkers Prev. 2008 Aug;17(8):2174-9. doi: 10.1158/1055-9965.EPI-07-2867.
Management of the patient with oral epithelial dysplasia depends on the ability to predict malignant transformation. Histologic grading of this condition fails in this regard and is also subject to interpathologist and intrapathologist variability. This study uses longitudinal clinical samples to explore the prognostic value of a previously validated panel of methylation biomarkers in a cohort of patients with histologically proven oral dysplasia. Methylation enrichment pyrosequencing assays were used to provide the sensitivity of traditional methylation-specific PCR with the additional specificity advantages of a subsequent confirmatory sequencing reaction. In 57% (8 of 14) patients with a lesion that transformed to oral squamous cell carcinoma, 26% (26 of 100) of longitudinal samples collected over > or =3 years showed p16 methylation. Only 1% (2 of 184) of samples from 8% of patients (2 of 24) not undergoing malignant transformation within 3 years had p16 methylation. Both of these samples with p16 promoter methylation were the most recently collected and the patients remain under continuing clinical review. Promoter methylation of MGMT, CYGB, and CCNA1 did not correlate with malignant progression. We thus conclude that methylation of the p16 gene promoter shows promise as a predictor for malignant transformation (Fisher's exact, P = 0.002) in a subset of patients.
口腔上皮发育异常患者的管理取决于预测恶性转化的能力。在这方面,这种情况的组织学分级并不成功,并且还存在病理学家之间以及同一病理学家内部的差异。本研究使用纵向临床样本,在一组经组织学证实为口腔发育异常的患者中,探索一组先前经验证的甲基化生物标志物的预后价值。甲基化富集焦磷酸测序分析用于提供传统甲基化特异性PCR的灵敏度,并具有后续验证性测序反应的额外特异性优势。在病变转化为口腔鳞状细胞癌的患者中,57%(14例中的8例)在≥3年期间收集的纵向样本中,有26%(100例中的26例)显示p16甲基化。在3年内未发生恶性转化的患者中,8%(24例中的2例)的样本中只有1%(184例中的2例)有p16甲基化。这两个p16启动子甲基化的样本都是最近收集的,这些患者仍在接受持续的临床检查。MGMT、CYGB和CCNA1的启动子甲基化与恶性进展无关。因此,我们得出结论,p16基因启动子的甲基化有望作为一部分患者恶性转化的预测指标(Fisher精确检验,P = 0.002)。