Korean J Pathol.
2000 Aug;34(8):541-549.
Genotype of Epstein-Barr Virus and Comparative Genomic Hybridization Analysis of NK/T Cell Lymphoma
- Affiliations
-
- 1Department of Diagnostic Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.
- 2Department of Diagnostic Pathology, Samsung Medical Center, Samsung Basic Research Institute, Seoul 135-710, Korea.
Abstract
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NK/T cell lymphoma is a distinct clinicopathologic entity which is more prevalent
in Asia than in America and Europe and is highly associated with Epstein-Barr virus
(EBV) infection. Although the clinicopathologic features of the tumor have been clearly
defined, genetic changes and roles of virus associated with the development and
progression of tumor have not been well studied. In this study, we carried out
polymerase chain reaction (PCR) for EBNA-3B, EBNA-3C, and LMP-1 30 bp deletion to
investigate EBV subtype and variants in tumor tissue and performed comparative
genomic hybridization (CGH) to screen chromosomal imbalances using frozen tissues
from 7 patients with nasal-type NK/T cell lymphoma and 1 patient with blastic NK cell
lymphoma. Of 6 cases infected with EBV, there were EBV type 1 in six, LMP-1 30 bp
deletion variant in four, and LMP-1 40 bp deletion variant in one. Frequent chromosomal
imbalances included deletions at 1p31-pter (4), 12q23-q24 (3), and 17p (4), and gains at
2q (5), 10q (3), and 13q34-qter (4). Blastic NK cell lymphoma displayed deletions of 9q,
7q, and 6q, similar to that of nasal-type NK/T-cell lymphoma. With these results, we
assumed that candidate genes in these imbalanced chromosomal loci would provide the
clue for further molecular studies to identify putative tumor suppressor genes or
proto-oncogenes associated with pathogenesis of this neoplasm.