The Epstein-Barr virus oncoprotein, latent membrane protein-1, reprograms germinal centre B cells towards a Hodgkin's Reed-Sternberg-like phenotype

被引:84
作者
Vockerodt, M. [1 ,2 ]
Morgan, S. L. [1 ]
Kuo, M. [3 ]
Wei, W. [1 ]
Chukwuma, M. B. [1 ]
Arrand, J. R. [1 ]
Kube, D. [4 ]
Gordon, J. [5 ]
Young, L. S. [1 ]
Woodman, C. B. [1 ]
Murray, P. G. [1 ]
机构
[1] Univ Birmingham, Sch Med, Canc Res UK Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
[2] Univ Gottingen, Zentrum Kinderheilkunde & Jugendmed, D-3400 Gottingen, Germany
[3] Birmingham Childrens Hosp, Dept Paediat Otolaryngol, Birmingham, W Midlands, England
[4] Univ Gottingen, Abt Hamatol & Onkol, Zentrum Innere Med, D-3400 Gottingen, Germany
[5] Univ Birmingham, Sch Med, MRC, Ctr Immune Regulat, Birmingham B15 2TT, W Midlands, England
关键词
Hodgkin's lymphoma; Epstein-Barr virus; latent membrane protein-1; germinal centre R cells; gene expression;
D O I
10.1002/path.2384
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although the latent membrane protein-1 (LMP1) of the Epstein-Barr virus (EBV) is believed to be important for the transformation of germinal centre (GC) B cells, the precise contribution of this viral oncogene to lymphoma development is poorly understood. In this study, we used a non-viral vector-based method to express LMP1 in primary human GC B cells. Gene expression profiling revealed that LMP1 induced in GC B cells transcriptional changes characteristic of Hodgkin's lymphoma cell lines. Strikingly, LMP1 down-regulated the expression of B-cell-specific genes including B-cell receptor components such as CD79A, CD79B, CD19, CD20, CD22, and BLNK. LMP1 also induced the expression of ID2, a negative regulator of B-cell differentiation. Our data suggest that in EBV-positive cases, LMP1 is likely to be a major contributor to the altered transcriptional pattern characteristic of Hodgkin/Reed-Sternberg cells, including the loss of B-cell identity. Copyright (C) 2008 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:83 / 92
页数:10
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