t(11;14)(q23;q32) involving IGH and DDX6 in nodal marginal zone lymphoma

BCL6公司 生物 染色体易位 基因敲除 淋巴瘤 节的 癌症研究 基因 遗传学 B细胞 免疫学 生发中心 抗体
作者
Susanne Stary,Ursula Vinatzer,Leonhard Müllauer,Markus Raderer,Peter Birner,Berthold Streubel
出处
期刊:Genes, Chromosomes and Cancer [Wiley]
卷期号:52 (1): 33-43 被引量:13
标识
DOI:10.1002/gcc.22004
摘要

Abstract Nodal marginal zone lymphoma (NMZL) is a primary nodal B‐cell lymphoma that shares morphological and immunophenotypic characteristics with extranodal and splenic marginal zone lymphoma. Data on altered genes and signaling pathways are scarce in this rare tumor entity. To gain further insights into the genetic background of NMZL, seven cases were investigated by microarray analysis, G‐banding, and FISH. Chromosomal imbalances were observed in 3/7 cases (43%) with gains of chromosome arms 1q, 8q, and 12q being the most frequent findings. Furthermore, we identified a translocation t(11;14)(q23;q32) involving IGH and DDX6 . Chromosomal walking, expression analysis, siRNA‐mediated gene knockdown and a yeast two hybrid screen were performed for further characterization of the translocation in vitro. In siRNA experiments, DDX6 appeared not to be involved in NF‐κB activation as frequently observed for genes promoting lymphomagenesis but was found to interfere with the expression of BCL6 and BCL2 in an NF‐κB independent manner. In conclusion, we identified several unbalanced aberrations and a t(11;14) involving IGH and DDX6 providing evidence for a contribution of DDX6 to lymphomagenesis by deregulation of BCL6 in NMZL. © 2012 Wiley Periodicals, Inc.
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