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阵列比较基因组杂交显示睾丸淋巴瘤中6号染色体长臂缺失的频率非常高。

Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.

作者信息

Bosga-Bouwer Anneke G, Kok Klaas, Booman Marije, Boven Ludolf, van der Vlies Pieter, van den Berg Anke, van den Berg Eva, de Jong Bauke, Poppema Sibrand, Kluin Philip

机构信息

Department of Clinical Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

出版信息

Genes Chromosomes Cancer. 2006 Oct;45(10):976-81. doi: 10.1002/gcc.20361.

DOI:10.1002/gcc.20361
PMID:16865685
Abstract

Despite the fact that numerous studies have been performed on diffuse large B-cell lymphoma (DLBCL), only few have concerned extranodal lymphomas occurring in the testis. We performed a cytogenetic and molecular study of 17 testicular non-Hodgkin lymphomas, of which 14 were proven primary DLBCL of the testis. Cytogenetic analysis revealed in 8 out of 11 evaluable cases a structural abnormality of the long arm of chromosome 6, with deletion or addition of material of unknown origin, and with breakpoints spanning the region 6q12-6q23. The cytogenetic findings were confirmed by fluorescent in situ hybridization (FISH) with a chromosome 6 painting probe. Using array based-comparative genomic hybridization on 16 evaluable cases, including 5 cases not tested by cytogenetics or FISH, 14 (88%) showed chromosome 6q deletions. We identified two regions of minimal deletion (RMD), at 104-113 Mb (6q16.3-q21) and 137.5-138.8 Mb (6q23.3), respectively. In one case, we observed a 2.7 Mb homozygous deletion ranging from 135.3 to 138.0 Mb that partly overlapped with the RMD at 6q23.3. Our study indicates that 6q deletions play a major pathogenetic role in DLBCL of the testis and that many of these deletions are part of unbalanced translocations.

摘要

尽管已经对弥漫性大B细胞淋巴瘤(DLBCL)进行了大量研究,但仅有少数研究关注发生在睾丸的结外淋巴瘤。我们对17例睾丸非霍奇金淋巴瘤进行了细胞遗传学和分子研究,其中14例被证实为原发性睾丸DLBCL。细胞遗传学分析显示,在11例可评估病例中的8例中,6号染色体长臂存在结构异常,有不明来源物质的缺失或增加,断点跨越6q12 - 6q23区域。细胞遗传学结果通过使用6号染色体涂染探针的荧光原位杂交(FISH)得以证实。在16例可评估病例中,包括5例未进行细胞遗传学或FISH检测的病例,使用基于阵列的比较基因组杂交技术,14例(88%)显示6号染色体q臂缺失。我们分别在104 - 113 Mb(6q16.3 - q21)和137.5 - 138.8 Mb(6q23.3)处鉴定出两个最小缺失区域(RMD)。在1例病例中,我们观察到一个2.7 Mb的纯合缺失,范围从135.3至138.0 Mb,部分与6q23.3处的RMD重叠。我们的研究表明,6号染色体q臂缺失在睾丸DLBCL中起主要致病作用,并且这些缺失中的许多是不平衡易位的一部分。

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Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.阵列比较基因组杂交显示睾丸淋巴瘤中6号染色体长臂缺失的频率非常高。
Genes Chromosomes Cancer. 2006 Oct;45(10):976-81. doi: 10.1002/gcc.20361.
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