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华氏巨球蛋白血症的候选基因:当前证据与研究

Candidate genes of Waldenström's macroglobulinemia: current evidence and research.

作者信息

Bianchi Giada, Sacco Antonio, Kumar Shaji, Rossi Giuseppe, Ghobrial Irene, Roccaro Aldo

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.

出版信息

Appl Clin Genet. 2013 Jul 17;6:33-42. doi: 10.2147/TACG.S42690. Print 2013.

Abstract

Waldenström's macroglobulinemia (WM) is a relatively uncommon, indolent malignancy of immunoglobulin M-producing B cells. The World Health Organization classifies it as a lymphoplasmacytic lymphoma and patients typically present with anemia, hepatosplenomegaly and diffuse lymphadenopathies. Historically, the genetic characterization of the disease has been hampered by the relatively low proliferative rate of WM cells, thus making karyotyping challenging. The use of novel technologies such as fluorescence in situ hybridization, gene array, and whole genome sequencing has contributed greatly to establishing candidate genes in the pathophysiology of WM and to identifying potential treatment targets, such as L265P MYD88. The discovery of microRNAs and the recognition of epigenetics as a major modulatory mechanism of oncogene expression and/or oncosuppressor silencing have aided in further understanding the pathogenesis of WM. Once thought to closely resemble multiple myeloma, a cancer of terminally differentiated, immunoglobulin-secreting plasma cells, WM appears to genetically cluster with other indolent B-cell lymphomas such as chronic lymphocytic leukemia/small cell lymphoma. The relative high incidence of familial cases of WM and other B-cell malignancies has been helpful in identifying high-risk gene candidates. In this review, we focus on the established genes involved in the pathogenesis of WM, with special emphasis on the key role of derangement of the nuclear factor kappa B signaling pathway and epigenetic mechanisms.

摘要

华氏巨球蛋白血症(WM)是一种相对罕见的、由产生免疫球蛋白M的B细胞构成的惰性恶性肿瘤。世界卫生组织将其归类为淋巴浆细胞淋巴瘤,患者通常表现为贫血、肝脾肿大和弥漫性淋巴结病。从历史上看,由于WM细胞的增殖率相对较低,该疾病的基因特征研究受到阻碍,因此染色体核型分析具有挑战性。荧光原位杂交、基因芯片和全基因组测序等新技术的应用,为确定WM病理生理学中的候选基因以及识别潜在治疗靶点(如L265P MYD88)做出了巨大贡献。微小RNA的发现以及表观遗传学作为癌基因表达和/或抑癌基因沉默的主要调节机制的确认,有助于进一步了解WM的发病机制。WM曾一度被认为与多发性骨髓瘤(一种终末分化的、分泌免疫球蛋白的浆细胞癌症)极为相似,但现在看来,它在基因上与其他惰性B细胞淋巴瘤(如慢性淋巴细胞白血病/小细胞淋巴瘤)聚类。WM和其他B细胞恶性肿瘤家族性病例的相对高发病率,有助于识别高危基因候选者。在本综述中,我们重点关注参与WM发病机制的已确定基因,特别强调核因子κB信号通路紊乱和表观遗传机制的关键作用。

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