Epstein-Barr virus (EBV)-positive pyothorax-associated lymphoma (PAL): chromosomal integration of EBV in a novel CD2-positive PAL B-cell line

被引:28
作者
Daibata, M [1 ]
Taguchi, T
Nemoto, Y
Saito, T
Machida, H
Imai, S
Miyoshi, I
Taguchi, H
机构
[1] Kochi Med Sch, Dept Med, Kochi 7838505, Japan
[2] Kochi Med Sch, Dept Anat, Kochi 7838505, Japan
[3] Kochi Med Sch, Dept Microbiol, Kochi 7838505, Japan
关键词
pyothorax-associated lymphoma; Epstein-Barr virus; integration; cell line; biphenotypic lymphoma;
D O I
10.1046/j.1365-2141.2002.03466.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pyothorax-associated lymphoma (PAL) is a clinico-pathological entity arising in the pleural cavity of patients with long-standing inflammatory pyothorax. PAL is closely associated with Epstein-Barr virus (EBV), but how this virus contributes to the development of the lymphoma is unknown. We have successfully obtained a novel EBV-infected PAL cell line, designated Pal-1. The cell line and its source coexpressed CD2 and CD20 molecules, but other representative B- and T-cell markers such as CD1, CD3, CD5, CD7, CD10 and CD19 were not found. The B-cell origin of Pal-1 cells was proven by rearrangement of the immunoglobulin heavy- and light-chain genes without rearranged T-cell receptor genes. Both the cell line and primary tumour cells carried monoclonal EBV genome. Although EBV genome is known to be maintained as circular extrachromosomal DNA, neither circular nor linear extrachromosomal EBV DNA was detectable in Pal-1 cells by in situ lysis gel analysis. Fluorescence in situ hybridization demonstrated viral integration at a marker chromosome mostly consisting of the centromere region of chromosome 1. The viral integration event may enhance a chromosomal instability at the insertion site. This cell line represents the first example of EBV integration in PAL and could enable the study of the potential role of integrated viral infection in the development of PAL as well as mechanism of the aberrant phenotype expression.
引用
收藏
页码:546 / 557
页数:12
相关论文
共 59 条
[1]   MALIGNANT-LYMPHOMA WITH DUAL B-CELL AND T-CELL MARKERS - ANALYSIS OF THE NEOPLASTIC-CELLS WITH MONOCLONAL-ANTIBODIES DIRECTED AGAINST T-CELL SUBSETS [J].
AISENBERG, AC ;
BLOCH, KJ ;
WILKES, BM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1981, 154 (05) :1709-1714
[2]  
ALSAATI T, 1992, BLOOD, V80, P209
[3]   Gammaherpesviruses and "hit-and-run" oncogenesis [J].
Ambinder, RF .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (01) :1-3
[4]  
Aozasa K, 1996, INT J HEMATOL, V65, P9
[5]   Human herpesvirus 6 (HHV-6)-positive Burkitt's lymphoma: Establishment of a novel cell line infected with HHV-6 [J].
Bandobashi, K ;
Daibata, M ;
Kamioka, M ;
Tanaka, Y ;
Kubonishi, I ;
Taguchi, H ;
Ohtsuki, Y ;
Miyoshi, I .
BLOOD, 1997, 90 (03) :1200-1207
[6]   BOTH EPSTEIN-BARR-VIRUS (EBV)-ENCODED TRANS-ACTING FACTORS, EB1 AND EB2, ARE REQUIRED TO ACTIVATE TRANSCRIPTION FROM AN EBV EARLY PROMOTER [J].
CHEVALLIERGRECO, A ;
MANET, E ;
CHAVRIER, P ;
MOSNIER, C ;
DAILLIE, J ;
SERGEANT, A .
EMBO JOURNAL, 1986, 5 (12) :3243-3249
[7]   Epstein-Barr virus infection. [J].
Cohen, JI .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (07) :481-492
[8]   ACTIVATION OF EXPRESSION OF LATENT EPSTEIN-BARR HERPESVIRUS AFTER GENE-TRANSFER WITH A SMALL CLONED SUBFRAGMENT OF HETEROGENEOUS VIRAL-DNA [J].
COUNTRYMAN, J ;
MILLER, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (12) :4085-4089
[9]   Antisense oligodeoxynucleotides against the BZLF1 transcript inhibit induction of productive Epstein-Barr virus replication [J].
Daibata, M ;
Enzinger, EM ;
Monroe, JE ;
Kilkuskie, RE ;
Field, AK ;
Mulder, C .
ANTIVIRAL RESEARCH, 1996, 29 (2-3) :243-260
[10]   EPSTEIN-BARR-VIRUS (EBV) REPLICATION AND EXPRESSIONS OF EA-D (BMRF1 GENE-PRODUCT), VIRUS-SPECIFIC DEOXYRIBONUCLEASE, AND DNA-POLYMERASE IN EBV-ACTIVATED AKATA CELLS [J].
DAIBATA, M ;
SAIRENJI, T .
VIROLOGY, 1993, 196 (02) :900-904