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首页> 外文期刊>Gastroenterology research and practice >The Methylation Status and Expression of Epstein-Barr Virus Early Genes BARF1 and BHRF1 in Epstein-Barr Virus-Associated Gastric Carcinomas
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The Methylation Status and Expression of Epstein-Barr Virus Early Genes BARF1 and BHRF1 in Epstein-Barr Virus-Associated Gastric Carcinomas

机译:Epstein-Barr病毒相关胃癌中Epstein-Barr病毒早期基因BARF1和BHRF1的甲基化状态和表达

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Epstein-Barr virus (EBV) is an important DNA virus which establishes latent infection in human malignancies. Expression of EBV-encoded genes in the associated tumors is strongly modulated by promoter CpG methylation of EBV genome. This study aimed to explore the methylation status of the promoters of EBV BamHI-A rightward frame 1 (BARF1) and BamHI-H rightward open reading frame 1 (BHRF1) and their influence on transcriptional expression, to further understand the roles of BARF1 and BHRF1 in the occurrence of EBV-associated cancer. We evaluated the methylation status of BARF1 and BHRF1 promoters in 43 EBV-associated gastric carcinoma (EBVaGC) tissues and EBV-positive cell lines. Their expressions were evaluated by real-time quantitative PCR. We found that the promoters of BARF1 and BHRF1 were methylated by varying degrees in different EBV-positive cell lines and were almost hypermethylated in all EBVaGC tissues. The methylation status of BARF1 and BHRF1 promoters were significantly reduced by 5-Aza-CdR along with the increasing gene expressions. Hypermethylation of Ap and Hp mediates the frequent silencing of BARF1 and BHRF1 in EBV-associated tumors, which could be reactivated by a demethylation agent, suggesting that promoter demethylation and activation is important for BARF1 and BHRF1 transcription and their further action.
机译:Epstein-Barr病毒(EBV)是一种重要的DNA病毒,其在人类恶性肿瘤中建立了潜在感染。通过EBV基因组的启动子CpG甲基化强烈调节相关肿瘤中EBV编码基因的表达。本研究旨在探讨EBV BamHI-A向右框架1(BARF1)和BamHI-H向右开放阅读框架1(BHRF1)的甲基化状态及其对转录表达的影响,以进一步了解BARF1和BHRF1的作用在eBV相关癌症的发生中。我们在43个EBV相关胃癌(EBVAGC)组织和EBV阳性细胞系中评估了Barf1和BHRF1启动子的甲基化状态。它们的表达是通过实时定量PCR评估的。我们发现,通过不同的EBV阳性细胞系中的不同程度甲基化的促进剂甲基化,并在所有EBVAGC组织中几乎高甲基化。将BarF1和BHRF1启动子的甲基化状态明显减少5-αzA-CDR以及增加的基因表达。 AP和HP的高甲基化介导BARF1和BHRF1在EBV相关肿瘤中的频繁沉默,这可以通过去甲基化剂重新激活,表明启动子去甲基化和活化对于BARF1和BHRF1转录很重要及其进一步的作用。

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