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华氏巨球蛋白血症中的表观基因组学

Epigenomics in Waldenstrom's macroglobulinaemia.

作者信息

Sacco Antonio, Fenotti Adriano, Bazzana Stefano, Imberti Luisa, Rossi Giuseppe, Patterson Christopher J, Treon Steven P, Ghobrial Irene M, Roccaro Aldo M

机构信息

ASST Spedali Civili, Department of Medical Oncology, CREA Laboratory, Brescia, Italy; Dana-Farber Cancer Institute, Department of Medical Oncology, Boston, MA, USA.

ASST Spedali Civili, SITRA, Brescia, Italy.

出版信息

Best Pract Res Clin Haematol. 2016 Jun;29(2):156-160. doi: 10.1016/j.beha.2016.08.022. Epub 2016 Sep 25.

Abstract

Epigenomics refers to study of the epigenome, which represents changes in gene expression that are not induced by DNA sequence aberrations. For instance, DNA methylation, histone acetylation and microRNAs may modulate gene expression without altering the gene sequence. Waldenström's macroglobulinaemia (WM) is a low-grade B-cell lymphoma, classified as lymphoplasmacytic lymphoma, characterized by the presence of clonal lymphoplasmacytic cells in the bone marrow and serum monoclonal immunoglobulin-M in the circulation. It is a rare disease and, although indolent, it remains incurable with a median overall survival of 5-6 years. Most patients succumb to disease progression. WM cells present with aberrant histone hypoacetylation that may be explained, at least in part, via deregulated microRNAs, thus suggesting the use of histone deacetylase inhibitors or microRNA-based therapies in this disease.

摘要

表观基因组学是指对表观基因组的研究,表观基因组代表了并非由DNA序列畸变所诱导的基因表达变化。例如,DNA甲基化、组蛋白乙酰化和微小RNA可能在不改变基因序列的情况下调节基因表达。华氏巨球蛋白血症(WM)是一种低度B细胞淋巴瘤,归类为淋巴浆细胞淋巴瘤,其特征是骨髓中存在克隆性淋巴浆细胞以及循环血液中存在血清单克隆免疫球蛋白M。它是一种罕见疾病,虽然进展缓慢,但仍然无法治愈,总体中位生存期为5至6年。大多数患者死于疾病进展。WM细胞存在异常的组蛋白低乙酰化,这至少部分可以通过微小RNA失调来解释,因此提示在这种疾病中可使用组蛋白去乙酰化酶抑制剂或基于微小RNA的疗法。

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