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鼻咽癌中爱泼斯坦-巴尔病毒编码的微小RNA的调控网络、表达谱及其潜在的靶宿主基因

Regulation network and expression profiles of Epstein-Barr virus-encoded microRNAs and their potential target host genes in nasopharyngeal carcinomas.

作者信息

Zeng ZhaoYang, Huang HongBin, Huang LiLi, Sun MengXi, Yan QiJia, Song YaLi, Wei Fang, Bo Hao, Gong ZhaoJian, Zeng Yong, Li Qiao, Zhang WenLing, Li XiaYu, Xiang Bo, Li XiaoLing, Li Yong, Xiong Wei, Li GuiYuan

机构信息

Hunan Provincial Tumor Hospital, Xiangya School of Medicine, Central South University, Changsha, 410013, China.

Key Laboratory of Carcinogenesis of Ministry of Health, Key Laboratory of Carcinogenesis and Cancer Invasion of Ministry of Education, Cancer Research Institute, Central South University, Changsha, 410078, China.

出版信息

Sci China Life Sci. 2014 Mar;57(3):315-326. doi: 10.1007/s11427-013-4577-y. Epub 2014 Feb 16.

Abstract

Epstein-Barr virus (EBV) is associated with nasopharyngeal carcinoma (NPC) tumorigenesis. However, the mechanism(s) connecting EBV infection and NPC remain unclear. Recently, a new class of EBV microRNAs (miRNAs) has been described. To determine how EBV miRNAs control the expression of host genes, and to understand their potential role in NPC tumorigenesis, we profiled the expression of 44 mature EBV miRNAs and potential host genes in NPC and non-tumor nasopharyngeal epithelial tissues. We found that 40 EBV miRNAs from the BART transcript were highly expressed in NPC. Analysis of potential BART miRNA target genes revealed that 3140 genes and several important pathways might be involved in the carcinogenesis of NPC. A total of 105 genes with potential EBV miRNA binding sites were significantly downregulated, suggesting that EBV miRNAs may regulate these genes and contribute to NPC carcinogenesis. An EBV miRNA and host gene regulation network was generated to provide useful clues for validating of EBV miRNA functions in NPC tumorigenesis.

摘要

爱泼斯坦-巴尔病毒(EBV)与鼻咽癌(NPC)的肿瘤发生有关。然而,连接EBV感染与NPC的机制仍不清楚。最近,一类新的EBV微小RNA(miRNA)已被描述。为了确定EBV miRNA如何控制宿主基因的表达,并了解它们在NPC肿瘤发生中的潜在作用,我们分析了44种成熟EBV miRNA和潜在宿主基因在NPC和非肿瘤鼻咽上皮组织中的表达。我们发现来自BART转录本的40种EBV miRNA在NPC中高表达。对潜在的BART miRNA靶基因的分析表明,3140个基因和几个重要途径可能参与了NPC的致癌过程。共有105个具有潜在EBV miRNA结合位点的基因显著下调,这表明EBV miRNA可能调节这些基因并促进NPC的致癌作用。构建了一个EBV miRNA与宿主基因调控网络,为验证EBV miRNA在NPC肿瘤发生中的功能提供了有用的线索。

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