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瓦尔登斯特伦巨球蛋白血症中的表观遗传学。

Epigenetics in Waldenström's macroglobulinemia.

机构信息

Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

出版信息

Epigenomics. 2010 Oct;2(5):691-6. doi: 10.2217/epi.10.42.

Abstract

Waldenström's macroglobulinemia (WM) is a low-grade B-cell lymphoma characterized by the presence of lymphoplasmacytic cells in the bone marrow and a serum monoclonal immunoglobulin, known as IgM, in the circulation. Although indolent, it remains incurable with a median overall survival of 5-6 years, and most patients succumb to disease progression. Cytogenetic and molecular studies on gene-expression analysis at the mRNA level have demonstrated minimal changes in WM cells. Therefore, multilevel characterization of this disease at the genetic and epigenetic level is required to improve our understanding of the underlying molecular changes that lead to the initiation and progression of this disease. In this study it has been demonstrated that WM patients present with a specific miRNA signature. Among deregulated miRNAs, miR-155 and miR-9* play a pivotal role in the pathogenesis of this disease.

摘要

华氏巨球蛋白血症(WM)是一种低级别 B 细胞淋巴瘤,其特征是骨髓中存在淋巴浆细胞和循环中存在单克隆免疫球蛋白 IgM。虽然该病呈惰性,但仍无法治愈,中位总生存期为 5-6 年,大多数患者死于疾病进展。对基因表达分析的细胞遗传学和分子研究在 mRNA 水平上表明 WM 细胞的变化很小。因此,需要对这种疾病进行遗传和表观遗传水平的多层次表征,以提高我们对导致该病发生和进展的潜在分子变化的理解。在这项研究中已经证明,WM 患者具有特定的 miRNA 特征。在失调的 miRNA 中,miR-155 和 miR-9*在该病的发病机制中发挥着关键作用。

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引用本文的文献

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