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慢性淋巴细胞白血病中 ATM 异常的发生率及其临床意义。

Incidence and clinical implications of ATM aberrations in chronic lymphocytic leukemia.

机构信息

Department of Internal Medicine, Division of Hematology and Oncology, University of Michigan, Ann Arbor, MI 48109-0936,

出版信息

Genes Chromosomes Cancer. 2012 Dec;51(12):1125-32. doi: 10.1002/gcc.21997. Epub 2012 Sep 6.

Abstract

A subset of chronic lymphocytic leukemia (CLL) carries mutations in ataxia telangiectasia mutated (ATM). Such ATM mutations may be particularly relevant in the setting of del11q, which invariably results in the deletion of one ATM allele. To improve our understanding of the frequency and type of ATM mutations that exist in CLL, we resequenced all ATM coding exons in 24 CLL with del11q using direct sequencing. We detected two missense mutations, resulting in an ATM mutation frequency of 8%; nonsense and frameshift mutations were not identified. Given the low ATM mutation frequency detected in this cohort, we proceeded with measurements of nonmutational ATM aberrations in CLL through analysis of the activation state of ATM in response to external irradiation. The phosphorylation state of ATM at Ser-1981 was measured using quantitative immunoblotting in purified CLL cells isolated from 251 CLL patients; data were normalized to simultaneous measurements of total ATM protein and actin. Resulting p-ATM/ATM and p-ATM/actin ratios were subsequently analyzed for prognostic significance inclusive and exclusive of TP53 exons 2-10 mutations. From these analyses, conducted in a large prospectively enrolled CLL patient cohort, neither the p-ATM/ATM nor the p-ATM/actin ratios were found to be prognostic for short survival. These data in aggregate demonstrate a low frequency of ATM aberrations in an unselected CLL cohort and do not support a major prognostic role for ATM aberrations in CLL, thus motivating renewed research efforts aimed at understanding the pathobiology of 11q deletions in CLL. © 2012 Wiley Periodicals, Inc.

摘要

一部分慢性淋巴细胞白血病(CLL)携带共济失调毛细血管扩张症突变(ATM)突变。在 del11q 的情况下,ATM 突变可能特别相关,因为它必然导致一个 ATM 等位基因的缺失。为了提高我们对存在于 CLL 中的 ATM 突变的频率和类型的理解,我们使用直接测序对 24 例具有 del11q 的 CLL 进行了所有 ATM 编码外显子的重测序。我们检测到两个错义突变,导致 ATM 突变频率为 8%;未发现无义和移码突变。鉴于在该队列中检测到的 ATM 突变频率较低,我们继续通过分析 ATM 在对外照射的反应中的激活状态来测量 CLL 中的非突变性 ATM 异常。使用定量免疫印迹法在从 251 例 CLL 患者中分离的纯化 CLL 细胞中测量 ATM 在 Ser-1981 的磷酸化状态;数据被标准化为同时测量总 ATM 蛋白和肌动蛋白。随后分析了 p-ATM/ATM 和 p-ATM/actin 比值,包括和不包括 TP53 外显子 2-10 突变的预后意义。从这些分析中,在一个大型前瞻性 CLL 患者队列中进行,p-ATM/ATM 和 p-ATM/actin 比值均未被发现对短期生存具有预后意义。这些数据表明在未选择的 CLL 队列中 ATM 异常的频率较低,并且不支持 ATM 异常在 CLL 中的主要预后作用,从而激发了旨在理解 CLL 中 11q 缺失的病理生物学的新的研究努力。©2012Wiley Periodicals,Inc.

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