Zettl Andreas, Ott German, Makulik Angela, Katzenberger Tiemo, Starostik Petr, Eichler Thorsten, Puppe Bernhard, Bentz Martin, Müller-Hermelink Hans Konrad, Chott Andreas
Department of Pathology, University of Würzburg, Germany.
Am J Pathol. 2002 Nov;161(5):1635-45. doi: 10.1016/S0002-9440(10)64441-0.
Genetic alterations in enteropathy-type T-cell lymphoma (ETL) are unknown so far. In this series, 38 cases of ETL were analyzed by comparative genomic hybridization (CGH). CGH revealed chromosomal imbalances in 87% of cases analyzed, with recurrent gains of genetic material involving chromosomes 9q (in 58% of cases), 7q (24%), 5q (18%), and 1q (16%). Recurrent losses of genetic material occurred on chromosomes 8p and 13q (24% each), and 9p (18%). In this first systematic genetic study on ETL, chromosomal gains on 9q (minimal overlapping region 9q33-q34) were found to be highly characteristic of ETL. Fluorescence in situ hybridization analysis on four cases of ETL, using a probe for 9q34, indicated frequent and multiple gains of chromosomal material at 9q34 (up to nine signals per case). Among 16 patients with ETL who survived initial disease presentation, patients with more than three chromosomal gains or losses (n = 11) followed a worse clinical course than those with three or less imbalances (n = 5). The observation of similar genetic alterations in ETL and in primary gastric (n = 4) and colonic (n = 1) T-cell lymphoma, not otherwise specified, is suggestive of a genetic relationship of gastrointestinal T-cell lymphomas at either localization.
迄今为止,肠病型T细胞淋巴瘤(ETL)的基因改变尚不明确。在本系列研究中,通过比较基因组杂交(CGH)分析了38例ETL。CGH显示,在87%的分析病例中存在染色体失衡,常见的遗传物质增加涉及9号染色体长臂(58%的病例)、7号染色体长臂(24%)、5号染色体长臂(18%)和1号染色体长臂(16%)。遗传物质的常见缺失发生在8号染色体短臂和13号染色体长臂(各占24%)以及9号染色体短臂(18%)。在这项关于ETL的首次系统性基因研究中,发现9号染色体长臂(最小重叠区域9q33 - q34)的染色体增加是ETL的高度特征性表现。对4例ETL进行荧光原位杂交分析,使用针对9q34的探针,结果表明9q34处频繁且多次出现染色体物质增加(每例多达9个信号)。在16例初次发病后存活的ETL患者中,染色体增加或缺失超过3处的患者(n = 11)的临床病程比染色体失衡3处或更少的患者(n = 5)更差。在ETL以及原发性胃(n = 4)和结肠(n = 1)T细胞淋巴瘤(未另作说明)中观察到相似的基因改变,提示胃肠道不同部位的T细胞淋巴瘤存在基因关联。