Yu Fenggang, Syn Nicholas L, Lu Yanan, Chong Qing Yun, Lai Junyun, Tan Wei Jian, Goh Boon Cher, MacAry Paul A, Wang Lingzhi, Loh Kwok Seng
Department of Otolaryngology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Front Oncol. 2021 Apr 7;11:626659. doi: 10.3389/fonc.2021.626659. eCollection 2021.
Epstein-Barr virus (EBV)-the prototypical human tumor virus-is responsible for 1-2% of the global cancer burden, but divergent strains seem to exist in different geographical regions with distinct predilections for causing lymphoid or epithelial malignancies. Here we report the establishment and characterization of Yu103, an Asia Pacific EBV strain with a highly remarkable provenance of being derived from nasopharyngeal carcinoma biopsy but subsequently propagated in human B-lymphoma cells and xenograft models. Unlike previously characterized EBV strains which are either predominantly B-lymphotropic or epitheliotropic, Yu103 evinces an uncanny capacity to infect and transform both B-lymphocytes and nasopharyngeal epithelial cells. Genomic and phylogenetic analyses indicated that Yu103 EBV lies midway along the spectrum of EBV strains known to drive lymphomagenesis or carcinogenesis, and harbors molecular features which likely account for its unusual properties. To our knowledge, Yu103 EBV is currently the only EBV isolate shown to drive human nasopharyngeal carcinoma and B-lymphoma, and should therefore provide a powerful novel platform for research on EBV-driven hematological and epithelial malignancies.
爱泼斯坦-巴尔病毒(EBV)——典型的人类肿瘤病毒——导致全球1%-2%的癌症负担,但不同毒株似乎存在于不同地理区域,对引发淋巴样或上皮性恶性肿瘤有不同偏好。在此,我们报告了Yu103的建立与特性,这是一种亚太地区的EBV毒株,其来源极为独特,源自鼻咽癌活检组织,随后在人B淋巴瘤细胞和异种移植模型中传代。与先前鉴定的主要嗜B淋巴细胞或嗜上皮细胞的EBV毒株不同,Yu103表现出一种不可思议的能力,能够感染并转化B淋巴细胞和鼻咽上皮细胞。基因组和系统发育分析表明,Yu103 EBV处于已知驱动淋巴瘤发生或致癌的EBV毒株谱系的中间位置,并具有可能解释其异常特性的分子特征。据我们所知,Yu103 EBV是目前唯一显示可引发人类鼻咽癌和B淋巴瘤的EBV分离株,因此应为研究EBV驱动的血液系统和上皮性恶性肿瘤提供一个强大的新型平台。