首页> 外文期刊>Japanese journal of clinical oncology. >Methylation status and expression of human telomerase reverse transcriptase mRNA in relation to hypermethylation of the p16 gene in colorectal cancers as analyzed by bisulfite PCR-SSCP.
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Methylation status and expression of human telomerase reverse transcriptase mRNA in relation to hypermethylation of the p16 gene in colorectal cancers as analyzed by bisulfite PCR-SSCP.

机译:通过亚硫酸氢盐PCR-SSCP分析大肠癌中p16基因超甲基化的甲基化状态和人类端粒酶逆转录酶mRNA的表达。

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BACKGROUND: The expression level of human telomerase reverse transcriptase (hTERT) is correlated with telomerase activity and is expressed at high levels in malignant tumors. It is of interest whether expression of hTERT is regulated by methylation of the CpG island in the promoter of the hTERT gene. We examined hTERT expression and methylation status of the hTERT and other genes including p16. METHODS: We analyzed methylation status by bisulfite treatment and polymerase chain reaction with single-strand conformation polymorphism analysis (PCR-SSCP) and expression of the hTERT by RT-PCR, in 13 cancer cell lines, eight white blood cell samples and 24 colorectal cancer tissues. RESULTS: In the cancer cell lines, hTERT was expressed and the CpG island of the hTERT promoter was methylated. Most colorectal cancer tissues showed similar results. The promoter of hTERT was methylated in six cases, partially methylated in 17 cases and unmethylated in one case. All cases with methylation of hMLH1 or p16 also showed methylation of hTERT; however, some of the cases lacking p16 methylation also had hTERT methylation. CONCLUSION: Increased expression of hTERT is related to hypermethylation of hTERT in colorectal cancerous tissues as well as some cancer cell lines and disconcordant with hypermethylation of p16.
机译:背景:人类端粒酶逆转录酶(hTERT)的表达水平与端粒酶活性相关,并在恶性肿瘤中高水平表达。令人感兴趣的是,hTERT的表达是否受到hTERT基因启动子中CpG岛甲基化的调节。我们检查了hTERT和其他基因(包括p16)的hTERT表达和甲基化状态。方法:我们分析了亚硫酸氢盐处理和聚合酶链反应与单链构象多态性分析(PCR-SSCP)的甲基化状态,并通过RT-PCR分析了hTERT在13个癌细胞系,8个白细胞样品和24个结直肠癌中的表达组织。结果:在癌细胞系中,hTERT被表达,hTERT启动子的CpG岛被甲基化。大多数结直肠癌组织显示出相似的结果。 hTERT的启动子被甲基化6例,部分甲基化17例,未甲基化1例。所有hMLH1或p16甲基化的病例也显示hTERT甲基化。但是,一些缺乏p16甲基化的病例也有hTERT甲基化。结论:hTERT表达的增加与大肠癌组织及某些癌细胞系中hTERT的高甲基化有关,并与p16的高甲基化不一致。

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