Hotchin N A, Wedderburn N, Roberts I, Thomas J A, Bungey J A, Naylor B, Crawford D H
Department of Clinical Sciences, London School of Hygiene and Tropical Medicine, UK.
Br J Cancer. 1993 May;67(5):926-32. doi: 10.1038/bjc.1993.172.
The respective roles of Epstein-Barr virus (EBV) and c-myc in the pathogenesis of endemic Burkitt's lymphoma (BL) are unclear. In order to help resolve the question whether constitutive expression of the c-myc gene in an EBV-immortalised B cell is sufficient to induce a tumorigenic phenotype, B cells from a common marmoset (Callithrix jacchus) were immortalised with EBV, transfected with a constitutively activated c-myc gene and inoculated into the host animals. Despite the cell line transfected with c-myc displaying enhanced growth characteristics, in vitro and in vivo experiments demonstrated that this was not sufficient to induce a tumorigenic phenotype. This supports our previous findings with EBV-immortalised human B cells transfected with an activated c-myc gene (Hotchin et al., 1990).
爱泼斯坦-巴尔病毒(EBV)和c-myc在地方性伯基特淋巴瘤(BL)发病机制中的各自作用尚不清楚。为了帮助解决c-myc基因在EBV永生化B细胞中的组成型表达是否足以诱导致瘤表型这一问题,将普通狨猴(Callithrix jacchus)的B细胞用EBV永生化,用组成型激活的c-myc基因转染,并接种到宿主动物体内。尽管转染了c-myc的细胞系显示出增强的生长特性,但体外和体内实验表明,这不足以诱导致瘤表型。这支持了我们之前对用激活的c-myc基因转染的EBV永生化人B细胞的研究结果(Hotchin等人,1990年)。