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Viral microRNA targetome of KSHV-infected primary effusion lymphoma cell lines.KSHV 感染的原发性渗出性淋巴瘤细胞系的病毒 microRNA 靶标组。
Cell Host Microbe. 2011 Nov 17;10(5):515-26. doi: 10.1016/j.chom.2011.09.012.
2
Contributions of the Epstein-Barr virus EBNA1 protein to gastric carcinoma.EBNA1 蛋白在胃癌中的作用。
J Virol. 2012 Jan;86(1):60-8. doi: 10.1128/JVI.05623-11. Epub 2011 Oct 19.
3
The members of an Epstein-Barr virus microRNA cluster cooperate to transform B lymphocytes.EB 病毒 microRNA 簇的成员合作转化 B 淋巴细胞。
J Virol. 2011 Oct;85(19):9801-10. doi: 10.1128/JVI.05100-11. Epub 2011 Jul 13.
4
Profiling of Epstein-Barr virus-encoded microRNAs in nasopharyngeal carcinoma reveals potential biomarkers and oncomirs.鼻咽癌中 Epstein-Barr 病毒编码 microRNAs 的分析揭示了潜在的生物标志物和致癌 miRNA。
Cancer. 2012 Feb 1;118(3):698-710. doi: 10.1002/cncr.26309. Epub 2011 Jun 30.
5
The Epstein-Barr Virus BART microRNAs target the pro-apoptotic protein Bim.EB 病毒 BART 微 RNA 靶向促凋亡蛋白 Bim。
Virology. 2011 Apr 10;412(2):392-400. doi: 10.1016/j.virol.2011.01.028. Epub 2011 Feb 18.
6
Characterization of Epstein-Barr virus miRNAome in nasopharyngeal carcinoma by deep sequencing.通过深度测序对鼻咽癌中 Epstein-Barr 病毒 miRNAome 的特征分析。
PLoS One. 2010 Sep 20;5(9):e12745. doi: 10.1371/journal.pone.0012745.
7
Micro RNAs of Epstein-Barr virus promote cell cycle progression and prevent apoptosis of primary human B cells.EB 病毒微小 RNA 促进原代人 B 细胞的细胞周期进程并阻止其凋亡。
PLoS Pathog. 2010 Aug 19;6(8):e1001063. doi: 10.1371/journal.ppat.1001063.
8
Systematic analysis of viral and cellular microRNA targets in cells latently infected with human gamma-herpesviruses by RISC immunoprecipitation assay.通过 RISC 免疫沉淀分析检测潜伏感染人类γ疱疹病毒的细胞中的病毒和细胞 microRNA 靶标进行系统分析。
Cell Host Microbe. 2010 Apr 22;7(4):324-334. doi: 10.1016/j.chom.2010.03.008.
9
Epstein-Barr virus (EBV)-encoded small RNA is released from EBV-infected cells and activates signaling from Toll-like receptor 3.爱泼斯坦-巴尔病毒(EBV)编码的小RNA从EBV感染的细胞中释放出来,并激活Toll样受体3的信号传导。
J Exp Med. 2009 Sep 28;206(10):2091-9. doi: 10.1084/jem.20081761. Epub 2009 Aug 31.
10
Widespread shortening of 3'UTRs by alternative cleavage and polyadenylation activates oncogenes in cancer cells.通过可变切割和多聚腺苷酸化导致的3'非翻译区广泛缩短会激活癌细胞中的致癌基因。
Cell. 2009 Aug 21;138(4):673-84. doi: 10.1016/j.cell.2009.06.016.

在胃腺癌细胞系中感染 Epstein-Barr 病毒可诱导细胞获得锚着独立性和基因表达的全局改变。

Infection of Epstein-Barr virus in a gastric carcinoma cell line induces anchorage independence and global changes in gene expression.

机构信息

Lineberger Comprehensive Cancer Center and Department of Microbiology-Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Proc Natl Acad Sci U S A. 2012 Jun 12;109(24):9593-8. doi: 10.1073/pnas.1202910109. Epub 2012 May 30.

DOI:10.1073/pnas.1202910109
PMID:22647604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3386136/
Abstract

Latent infection of EBV is linked to the development of multiple cancers that have distinct patterns of expression of viral proteins and microRNAs (miRNAs). In this study, we show that in vitro infection of a gastric epithelial cell line with EBV alters growth properties and induces growth in soft agar. The infected cells have high levels of expression of a large cluster of viral miRNAs, [the BamHI A rightward transcript (BART) miRNAs] and limited viral protein expression. Expression profile microarray analysis of this cell line revealed a large number of changes in cellular expression, with decreased expression of many genes. Inhibition of the trace-expressed levels of the viral oncoprotein, latent membrane protein 1, did not affect growth or alter the pattern of cellular expression. The expression changes are highly enriched for genes involved in cell motility and transformation pathways, suggesting these changes are important for the altered growth phenotype. Importantly, the transcripts decreased by microarray are significantly enriched in both experimentally and bioinformatically predicted BART miRNA targets. The absence of viral protein expression and the enrichment for viral miRNA targets in the modulated cell genes suggest that the BART miRNAs are major contributors to the transformed growth properties of the EBV-infected cells. The ability to affect cell growth through miRNA expression without viral protein expression would be a major factor in the development of cancer in individuals with functional immune systems.

摘要

EBV 的潜伏感染与多种癌症的发展有关,这些癌症的病毒蛋白和 microRNAs(miRNAs)表达模式不同。在这项研究中,我们表明,体外感染 EBV 会改变胃上皮细胞系的生长特性,并诱导其在软琼脂中生长。受感染的细胞高水平表达一大簇病毒 miRNAs(BamHI A 右向转录物(BART)miRNAs),而病毒蛋白表达有限。对该细胞系的表达谱微阵列分析显示,细胞表达发生了大量变化,许多基因的表达下调。抑制痕量表达的病毒癌蛋白潜伏膜蛋白 1 并不影响生长或改变细胞表达模式。表达变化高度富集参与细胞运动和转化途径的基因,表明这些变化对于改变的生长表型很重要。重要的是,通过微阵列下调的转录物在实验和生物信息学预测的 BART miRNA 靶标中显著富集。调节细胞基因中缺乏病毒蛋白表达和 BART miRNA 靶标的富集表明,BART miRNAs 是 EBV 感染细胞转化生长特性的主要贡献者。通过 miRNA 表达而不表达病毒蛋白来影响细胞生长的能力将是免疫系统功能正常的个体癌症发展的一个主要因素。