Rosas S L, Koch W, da Costa Carvalho M G, Wu L, Califano J, Westra W, Jen J, Sidransky D
Department of Otolaryngology, Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland 21206-2198, USA.
Cancer Res. 2001 Feb 1;61(3):939-42.
Aberrant promoter hypermethylation is common in head and neck cancer and may be useful as a marker for cancer cells. We examined whether cells with tumor-specific aberrant DNA-methylation might be found in the saliva of affected patients. We tested 30 patients with primary head and neck tumors using methylation-specific PCR searching for promoter hypermethylation of the tumor suppressor gene p16 (CDKN2A), the DNA repair gene O6-methylguanine-DNA-methyltransferase (MGMT) and the putative metastasis suppressor gene death-associated protein kinase (DAP-K). Aberrant methylation of at least one of these genes was detected in 17 (56%) of 30 head and neck primary tumors; 14 (47%) of 30 at p16, 10 (33%) of 30 at Dap-K and 7 (23%) of 30 at MGMT. In 11 (65%) of 17 methylated primary tumors abnormal methylated DNA was detected in the matched saliva samples. Abnormal promoter methylation in saliva DNA was found in all tumor stages and more frequently in tumors located in the oral cavity. Moreover, none of the saliva from patients with methylation-negative tumors displayed methylation of any marker. Of 30 saliva samples from healthy control subjects (15 smokers and 15 nonsmokers), only one sample from a smoking patient was positive for DNA methylation at two target genes. Detection of aberrant promoter hypermethylation patterns of cancer-related genes in saliva of head and cancer patients is feasible and may be potentially useful for detecting and monitoring disease recurrence. Long-term longitudinal studies are needed to evaluate this approach for early detection of head and neck cancer in at-risk populations.
异常启动子高甲基化在头颈癌中很常见,可能作为癌细胞的一个标志物。我们研究了在受影响患者的唾液中是否能发现具有肿瘤特异性异常DNA甲基化的细胞。我们使用甲基化特异性PCR检测了30例原发性头颈肿瘤患者,寻找肿瘤抑制基因p16(CDKN2A)、DNA修复基因O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)和假定的转移抑制基因死亡相关蛋白激酶(DAP-K)的启动子高甲基化。在30例原发性头颈肿瘤中,17例(56%)检测到至少其中一个基因的异常甲基化;p16基因在30例中有14例(47%),Dap-K基因在30例中有10例(33%),MGMT基因在30例中有7例(23%)。在17例甲基化原发性肿瘤中的11例(65%)的匹配唾液样本中检测到异常甲基化DNA。在所有肿瘤分期的唾液DNA中均发现异常启动子甲基化,在口腔肿瘤中更为常见。此外,甲基化阴性肿瘤患者的唾液中均未显示任何标志物的甲基化。在30例健康对照受试者(15名吸烟者和1�名不吸烟者)的唾液样本中,只有1例来自吸烟患者的样本在两个靶基因处DNA甲基化呈阳性。检测头颈癌患者唾液中癌症相关基因的异常启动子高甲基化模式是可行的,可能对检测和监测疾病复发有潜在作用。需要进行长期纵向研究以评估这种方法在高危人群中对头颈癌的早期检测效果。