Viswanathan Muthusamy, Tsuchida Nobuo, Shanmugam Govindaswamy
Cancer Biology Division, Centre of Excellence in Genomic Studies, School of Biological Sciences, Madurai Kamaraj University, Madurai, India.
Int J Cancer. 2003 May 20;105(1):41-6. doi: 10.1002/ijc.11028.
Aberrant promoter hypermethylation of tumor-associated genes leading to their inactivation is a common event in many cancer types. Using a sensitive restriction-multiplex PCR method, we studied the promoter hypermethylation profile of the p16, p15, hMLH1, MGMT and E-cad genes in oral squamous cell carcinoma (OSCC) of Indians. We analyzed a total of 51 samples for the p15 tumor-suppressor gene and 99 samples for each of the remaining genes. Our studies indicate an incidence of promoter hypermethylation of 23% each for p16 and p15, 8% for hMLH1, 41% for MGMT and 35% for E-cad. We observed aberrant hypermethylation of the promoter region of at least 1 of these genes in 74.5% of cases (n = 51) for which all the 5 genes were studied. Abnormal methylation was detected in tumors irrespective of stage and location in the oral cavity, whereas no abnormal methylation was detectable in normal oral squamous tissues obtained from 25 OSCC patients. Detection of aberrant hypermethylation patterns of cancer-associated genes listed above is therefore suitable for diagnosis of OSCC in individuals at high risk for this disease.
肿瘤相关基因的异常启动子高甲基化导致其失活,这在许多癌症类型中是常见事件。我们使用一种灵敏的限制性多重聚合酶链反应方法,研究了印度人口腔鳞状细胞癌(OSCC)中p16、p15、hMLH1、MGMT和E-cad基因的启动子高甲基化谱。我们总共分析了51个样本中的p15肿瘤抑制基因,以及其余每个基因的99个样本。我们的研究表明,p16和p15的启动子高甲基化发生率均为23%,hMLH1为8%,MGMT为41%,E-cad为35%。在研究了所有5个基因的74.5%的病例(n = 51)中,我们观察到这些基因中至少有1个基因的启动子区域存在异常高甲基化。无论口腔癌的分期和位置如何,肿瘤中均检测到异常甲基化,而从25例OSCC患者获取的正常口腔鳞状组织中未检测到异常甲基化。因此,检测上述癌症相关基因的异常高甲基化模式适用于对该疾病高危个体的OSCC诊断。