Lineberger Comprehensive Cancer Center and Department of Microbiology-Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.
Proc Natl Acad Sci U S A. 2012 Jun 12;109(24):9593-8. doi: 10.1073/pnas.1202910109. Epub 2012 May 30.
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.
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。