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巢式甲基化特异性PCR 检测食管癌病人血清中p16 基因启动子区过甲基化

Detection of Promoter Hypermethylation in the Serum of Esophageal Squamous Cell Carcinoma Patients by Nested Methylation-Specific-Polymerase Chain Reaction

  • 摘要: 目的 检测食管鳞状细胞癌(squamous cell carcinoma,SCC)患者外周血血清中p16基因启动子区的甲基化状态,探讨p16基因启动子的过甲基化在食管鳞状细胞癌筛查及早期诊断中的意义。方法 利用巢式甲基化特异性PCR(nMSP)法检测食管鳞状细胞癌患者外周血血清与正常人血清中p16基因启动子的甲基化状态,并与普通甲基化特异性PCR(MSP)法进行了比较。结果 56例SCC血清样品中nMSP法发现34例p16基因启动子的过甲基化,MSP法只检出15例,而22例正常人血清中都未检测到p16基因启动子的过甲基化。测序结果进一步验证了方法的可靠性。结论 利用巢式MSP(nMSP)法检测外周血血清中p16基因启动子的甲基化,可为食管癌的筛查、早期诊断及预后判断提供有价值的信息。

     

    Abstract: Objective  This study was designed to detect the methylation status of the promoter region of p16 gene in DNA extracted serum from esophageal squamous cell carcinoma (SCC), and evaluate the role of p16 gene promoter hypermethylation in esophageal SCC screening and early diagnosis. Methods  Nested methylation-specific PCR (nMSP) was used to detect p16 promoter hypermethylation in serum DNA from 56 esophageal squamous cell carcinoma (SCC) and cont rol serum samples from 22 healthy individuals. Compared methylation-specific PCR(MSP), nMSP was more sensitive. Results  Aberrant promoter rmethylation of the p16 gene was found in 34 of 56 serum samples using nMSP, and only 15 cases was detected using MSP. No aberrant promoter methylation was detected in the peripheral serum of the healthy individuals. Conclusion  The detection of p16 gene promoter hypermethylation in the serum of esophageal SCC patient s can give the useful information for tumor early diagnosis, follow-up study of esophageal SCC patient s. nMSP is a simple, sensitive, and specific method for rapid analysis of the promoter methylation status of many genes.

     

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