4.7 Article

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

Journal

JOURNAL OF PATHOLOGY
Volume 216, Issue 1, Pages 83-92

Publisher

JOHN WILEY & SONS LTD
DOI: 10.1002/path.2384

Keywords

Hodgkin's lymphoma; Epstein-Barr virus; latent membrane protein-1; germinal centre R cells; gene expression

Funding

  1. Leukaemia Research Fund, Cancer Research UK
  2. Birmingham Children's Hospital Research Foundation
  3. UICC Yamagiwa-Yoshida Memorial International Cancer Study Grant (MV)
  4. Royal College of Pathologists/Cancer Research UK Clinical Training Fellowship (SLM)

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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.

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