Tsao Sai-Wah, Tsang Chi Man, To Ka-Fai, Lo Kwok-Wai
Department of Anatomy and Centre for Cancer Research, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong SAR.
J Pathol. 2015 Jan;235(2):323-33. doi: 10.1002/path.4448.
The close association of Epstein-Barr virus (EBV) infection with non-keratinizing nasopharyngeal carcinomas and a subset of gastric carcinomas suggests that EBV infection is a crucial event in these cancers. The difficulties encountered in infecting and transforming primary epithelial cells in experimental systems suggest that the role of EBV in epithelial malignancies is complex and multifactorial in nature. Genetic alterations in the premalignant epithelium may support the establishment of latent EBV infection, which is believed to be an initiation event. Oncogenic properties have been reported in multiple EBV latent genes. The BamH1 A rightwards transcripts (BARTs) and the BART-encoded microRNAs (miR-BARTs) are highly expressed in EBV-associated epithelial malignancies and may induce malignant transformation. However, enhanced proliferation may not be the crucial function of EBV infection in epithelial malignancies, at least in the early stages of cancer development. EBV-encoded gene products may confer anti-apoptotic properties and promote the survival of infected premalignant epithelial cells harbouring genetic alterations. Multiple EBV-encoded microRNAs have been reported to have immune evasion functions. Genetic alterations in host cells, as well as inflammatory stroma, could modulate the expression of EBV genes and alter the growth properties of infected premalignant epithelial cells, encouraging their selection during carcinogenesis.
爱泼斯坦-巴尔病毒(EBV)感染与非角化鼻咽癌及一部分胃癌密切相关,这表明EBV感染是这些癌症中的关键事件。在实验系统中感染和转化原代上皮细胞时遇到的困难表明,EBV在上皮恶性肿瘤中的作用本质上是复杂且多因素的。癌前上皮细胞中的基因改变可能支持潜伏性EBV感染的建立,而这被认为是起始事件。多个EBV潜伏基因已被报道具有致癌特性。BamH1 A向右转录本(BARTs)和BART编码的微小RNA(miR-BARTs)在EBV相关的上皮恶性肿瘤中高度表达,并可能诱导恶性转化。然而,至少在癌症发展的早期阶段,增殖增强可能不是EBV感染在上皮恶性肿瘤中的关键功能。EBV编码的基因产物可能赋予抗凋亡特性,并促进携带基因改变的感染癌前上皮细胞的存活。多个EBV编码的微小RNA已被报道具有免疫逃避功能。宿主细胞以及炎性基质中的基因改变可调节EBV基因的表达,并改变感染癌前上皮细胞的生长特性,促进它们在致癌过程中的选择。