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p16INK4a/CDKN2A基因失活可能是皮肤B细胞淋巴瘤中腿部大B细胞淋巴瘤的一个诊断特征。

Inactivation of p16INK4a/CDKN2A gene may be a diagnostic feature of large B cell lymphoma leg type among cutaneous B cell lymphomas.

作者信息

Belaud-Rotureau Marc-Antoine, Marietta Virginie, Vergier Beatrice, Mainhaguiet Guillaume, Turmo Michelle, Idrissi Yamina, Ferrer Jacky, Beylot-Barry Marie, Dubus Pierre, Merlio Jean-Philippe

机构信息

EA 2406 Histologie et Pathologie Moléculaire des Tumeurs, Université Victor Segalen, Batiment 3B, 2ème étage, 146 rue Leo saignat, 33076 Bordeaux Cedex, France.

出版信息

Virchows Arch. 2008 Jun;452(6):607-20. doi: 10.1007/s00428-008-0593-x. Epub 2008 Mar 1.

Abstract

The World Health Organization-European Organization for Research and Treatment of Cancer has individualized three main categories among the primary cutaneous B cell lymphoma (PCBCL): leg-type primary cutaneous large B cell lymphoma (PCLBCL leg type), primary cutaneous follicle center lymphoma (PCFCL), and primary cutaneous marginal zone lymphoma (PCMZL). The genetic features of 21 PCBCL cases (six PCLBCL leg type four PCFCL large cells, seven PCFCL small cells, and four PCMZL) were investigated by comparative genomic hybridization (CGH array). Fluorescent in situ hybridization (FISH) analysis was performed to confirm CGH array data and to detect lymphoma-associated gene rearrangements. p14(ARF)/p16(INK4a) CDKN2A gene quantification, methylation analysis, and immunohistochemical detection were also performed. CGH array showed a higher number of recurrent genetic imbalances in PCLBCL leg type (mean 62) than in PCFCL large cells (mean 34). PCFCL small cells and PCMZL exhibited fewer chromosomal alterations (mean 24 and 9). FISH analysis provided concordant results with CGH array data in 97% (98 of 101) assays and demonstrated a t(8;14)(q24;q32) in two of six PCLBCL leg type. Recurrent deletions in 9p21 (p14(ARF)/p16(INK4a)CDKN2A) were a constant finding in PCLBCL leg type (six of six). Conversely, PCFCL large cells exhibited recurrent 1p36 deletions (four of four) without deletion in 9p21 (zero of four). The diagnostic and prognostic impact of the p16(INK4a)CDKN2A gene status in PCBCL should therefore be confirmed on a larger series.

摘要

世界卫生组织-欧洲癌症研究与治疗组织已将原发性皮肤B细胞淋巴瘤(PCBCL)分为三大主要类别:腿部型原发性皮肤大B细胞淋巴瘤(PCLBCL腿部型)、原发性皮肤滤泡中心淋巴瘤(PCFCL)和原发性皮肤边缘区淋巴瘤(PCMZL)。通过比较基因组杂交(CGH阵列)研究了21例PCBCL病例(6例PCLBCL腿部型、4例PCFCL大细胞型、7例PCFCL小细胞型和4例PCMZL)的基因特征。进行荧光原位杂交(FISH)分析以确认CGH阵列数据并检测淋巴瘤相关基因重排。还进行了p14(ARF)/p16(INK4a) CDKN2A基因定量、甲基化分析和免疫组织化学检测。CGH阵列显示,PCLBCL腿部型(平均62个)的复发性基因失衡数量高于PCFCL大细胞型(平均34个)。PCFCL小细胞型和PCMZL的染色体改变较少(平均24个和9个)。FISH分析在97%(101次检测中的98次)的检测中与CGH阵列数据结果一致,并在6例PCLBCL腿部型中的2例中显示出t(8;14)(q24;q32)。9p21(p14(ARF)/p16(INK4a)CDKN2A)的复发性缺失在PCLBCL腿部型中是一个恒定的发现(6例中的6例)。相反,PCFCL大细胞型表现出复发性1p36缺失(4例中的4例),而9p21无缺失(4例中的0例)。因此,p16(INK4a)CDKN2A基因状态在PCBCL中的诊断和预后影响应在更大的系列研究中得到证实。

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