Schop Roelandt F J, Fonseca Rafael
Mayo Clinic, Department of Hematology and Internal Medicine, Rochester, MN, USA.
Semin Oncol. 2003 Apr;30(2):142-5. doi: 10.1053/sonc.2003.50075.
Waldenstrom's macroglobulinemia (WM) is a clonal B-cell disorder characterized by the production of a monoclonal paraprotein and lymphoplasmacytic clonal expansion. The genetic basis of this disorder is poorly understood. We have recently found that the genetic makeup of WM cells is different from that commonly reported for multiple myeloma (MM), follicular lymphoma, and B-cell chronic lymphocytic leukemia. Translocations involving the immunoglobulin heavy chain locus (IgH) translocations could not be detected in any case, and a molecular analysis showed that the IgH locus switch mu retained its germline configuration. Aneuploidy was not detected using chromosome enumeration probes. The only recurrent chromosome abnormality found was deletion of 6q21. The lack of legitimate of illegitimate rearrangements at the IgH locus suggests that other mechanisms are involved in the pathogenesis of the disorder. Given the clear evidence of a familial form of WM and the currently presumed genomic stability of the clonal cells, it is likely that a single gene defect may be responsible for disease pathogenesis. Having found deletions of the long arm of chromosome 6 as the only recurrent aberration, we speculate that a gene involved in B-cell maturation or survival at this locus may be inactivated as a cause of WM.
华氏巨球蛋白血症(WM)是一种克隆性B细胞疾病,其特征为产生单克隆副蛋白和淋巴浆细胞克隆性增殖。该疾病的遗传基础尚不清楚。我们最近发现,WM细胞的基因构成与多发性骨髓瘤(MM)、滤泡性淋巴瘤和B细胞慢性淋巴细胞白血病通常报道的情况不同。在任何病例中均未检测到涉及免疫球蛋白重链基因座(IgH)的易位,分子分析表明IgH基因座的转换μ保留了其种系构型。使用染色体计数探针未检测到非整倍体。发现的唯一复发性染色体异常是6q21缺失。IgH基因座缺乏合法或非法重排表明该疾病的发病机制涉及其他机制。鉴于WM存在家族性形式的明确证据以及目前假定的克隆细胞基因组稳定性,很可能单个基因缺陷是疾病发病的原因。由于发现6号染色体长臂缺失是唯一的复发性畸变,我们推测该基因座上参与B细胞成熟或存活的一个基因可能因WM而失活。