Interphase cytogenetic analysis of lymphoma-associated chromosomal breakpoints in primary diffuse large B-cell lymphomas of the central nervous system

被引:59
作者
Montesinos-Rongen, M
Zühlke-Jenisch, R
Gesk, S
Martín-Subero, JI
Schaller, C
Van Roost, D
Wiestler, OD
Deckert, M
Siebert, R
机构
[1] Univ Cologne, Dept Neuropathol, Cologne, Germany
[2] Univ Hosp Kiel, Inst Human Genet, Kiel, Germany
[3] Univ Bonn, Ctr Med, Dept Neurosurg, D-5300 Bonn, Germany
[4] Univ Bonn, Ctr Med, Dept Neuropathol, D-5300 Bonn, Germany
关键词
cytogenetics; diffuse large B-cell lymphoma (DLBCL); lymphoma; primary central nervous system lymphoma (PCNSL); translocation;
D O I
10.1093/jnen/61.10.926
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Primary central nervous system lymphomas (PCNSLs) are germinal center-derived diffuse large B-cell lymphomas (DLBCLs) arising in and remaining confined to the brain, the pathogenesis of which is poorly understood, WC investigated 13 PCNSLs from immunocompetent patients by means of interphase cytogenetics on cryopreserved cells derived front stereotactic biopsies. Inter-phase fluorescence in situ hybridization (FISH) was performed for the detection of structural alterations affecting the IGH (14q32). IGK (2p12). IGL (22q11). BCL6 (3q27). MYC (8q24) CCND1 (11q13). MET and BCl.2 (both 18q21) loci. Signal constellations indicating break-points within the IGH and IGK locus were detected in 5 and 1 PCNSLs. respectively. There was no evidence for a t(8;14), t( 11:14), or t(14: 19) in this series of tumors, Breakpoints in the BCL6 locus were observed in 3 of the 13 cases. and nuclear Bcl-6 protein expression was detected in 6 of 9 PCNSLs, including those with genomic alterations of the encoding locus. Gains of 18q21 represented the most frequent imbalances present in more than one third of all cases. Interestingly, these gains included the MLT gene. Thus, this study provides the first evidence for recurrent chromosomal translocations in PCNSLs. While they share similarities with extracerebral DLBCL with respect to the presence of IGH translocations they appear to differ in the usage of translocation partner genes, which remain to he identified.
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页码:926 / 933
页数:8
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