Dierlamm J, Baens M, Stefanova-Ouzounova M, Hinz K, Wlodarska I, Maes B, Steyls A, Driessen A, Verhoef G, Gaulard P, Hagemeijer A, Hossfeld D K, De Wolf-Peeters C, Marynen P
Department of Oncology and Hematology, University Hospital Eppendorf, Hamburg, Germany.
Blood. 2000 Sep 15;96(6):2215-8.
The translocation of chromosome 11, long arm, region 2, band 1, to chromosome 18, long arm, region 2, band 1 (t(11;18)(q21;q21)) represents a recurrent chromosomal abnormality in extranodal marginal zone B-cell lymphoma (MZBCL) of mucosa-associated lymphoid tissue (MALT) type and leads to a fusion of the apoptosis inhibitor-2 (API2) gene on chromosome 11 and the MALT lymphoma-associated translocation (MLT) gene on chromosome 18. A 2-color fluorescence in situ hybridization (FISH) assay, which can be used for the detection of t(11;18) in interphase nuclei and metaphase chromosomes on fresh and archival tumor tissue, was developed. The P1 artificial chromosome (PAC) clone located immediately telomeric to the MLT gene and the PAC clone spanning the API2 gene were differentially labeled and used to visualize the derivative chromosome 11 resulting from t(11;18), as evident by the overlapping or juxtaposed red and green fluorescent signals. The assay was applied to interphase nuclei of 20 cases with nonmalignant conditions and 122 B-cell non-Hodgkin's lymphomas (NHLs). The latter group comprised 20 cases of nodal follicle center cell lymphoma and diffuse large B-cell NHL, 10 cases of gastric diffuse large B-cell lymphoma, 10 cases of hairy cell leukemia, and 82 cases of MZBCL (41 extranodal from various locations, 19 nodal, and 22 splenic MZBCL) including 35 cases with an abnormal karyotype, 2 of which revealed t(11;18). By interphase FISH, t(11;18) was detected in 8 gastrointestinal low-grade MALT-type lymphomas including the 2 cytogenetically t(11;18)(+) cases. In the 8 t(11;18)(+) cases, the FISH results were confirmed by reverse transcriptase-polymerase chain reaction (RT-PCR) using API2 and MLT specific primers. Our results indicate that t(11;18)(q21;q21) specifically characterizes a subgroup of low-grade MZBCL of the MALT-type and that the FISH assay described here is a highly specific and rapid test for the detection of this translocation.
11号染色体长臂2区1带易位至18号染色体长臂2区1带(t(11;18)(q21;q21))是黏膜相关淋巴组织(MALT)型结外边缘区B细胞淋巴瘤(MZBCL)中一种常见的染色体异常,会导致11号染色体上的凋亡抑制因子2(API2)基因与18号染色体上的MALT淋巴瘤相关易位(MLT)基因融合。开发了一种双色荧光原位杂交(FISH)检测方法,可用于在新鲜和存档肿瘤组织的间期核及中期染色体中检测t(11;18)。对紧邻MLT基因端粒的P1人工染色体(PAC)克隆和跨越API2基因的PAC克隆进行差异标记,用于可视化由t(11;18)产生的衍生11号染色体,红色和绿色荧光信号重叠或并置即可证明。该检测方法应用于20例非恶性疾病患者及122例B细胞非霍奇金淋巴瘤(NHL)患者的间期核。后一组包括20例淋巴结滤泡中心细胞淋巴瘤和弥漫性大B细胞NHL、10例胃弥漫性大B细胞淋巴瘤、10例毛细胞白血病以及82例MZBCL(41例来自不同部位的结外、19例淋巴结及22例脾脏MZBCL),其中35例核型异常,2例显示t(11;18)。通过间期FISH,在8例胃肠道低级别MALT型淋巴瘤中检测到t(11;18),包括2例细胞遗传学检测为t(11;18)(+)的病例。在8例t(11;18)(+)病例中,使用API2和MLT特异性引物通过逆转录聚合酶链反应(RT-PCR)证实了FISH结果。我们的结果表明,t(11;18)(q21;q21)是MALT型低级别MZBCL一个亚组的特异性特征,并且此处描述的FISH检测方法是检测该易位的一种高度特异性和快速的检测方法。