无细胞DNA 5-羟甲基胞嘧啶对急性髓系白血病的MRD评估高度敏感。

IF 5.7 2区 医学 Q1 Medicine
Jianming Shao, Shilpan Shah, Siddhartha Ganguly, Youli Zu, Chuan He, Zejuan Li
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引用次数: 0

摘要

可测量残留病(MRD)是急性髓性白血病(AML)的重要生物标志物。然而,目前的方法无法在许多患者中检测到MRD。通过分析115名AML患者和86名对照,我们在无细胞DNA中发现了高度敏感的5-羟甲基胞嘧啶(5hmC)特征。5hmC方法对29例MRD阴性患者中的20例(多参数流式细胞术)和14例MRD阴性患者中的11例(分子法)进行MRD检测。5hmC方法的MRD检测与无复发生存率显著相关。这种新方法可用于大多数AML患者,并可能对AML患者的管理产生重大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cell-free DNA 5-hydroxymethylcytosine is highly sensitive for MRD assessment in acute myeloid leukemia.

Cell-free DNA 5-hydroxymethylcytosine is highly sensitive for MRD assessment in acute myeloid leukemia.

Cell-free DNA 5-hydroxymethylcytosine is highly sensitive for MRD assessment in acute myeloid leukemia.

Measurable residual disease (MRD) is an important biomarker in acute myeloid leukemia (AML). However, MRD cannot be detected in many patients using current methods. We developed a highly sensitive 5-hydroxymethylcytosine (5hmC) signature in cell-free DNA by analyzing 115 AML patients and 86 controls. The 5hmC method detected MRD in 20 of 29 patients with negative MRD by multiparameter flow cytometry and 11 of 14 patients with negative MRD by molecular methods. MRD detection by the 5hmC method was significantly associated with relapse-free survival. This novel method can be used in most AML patients and may significantly impact AML patient management.

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来源期刊
Clinical Epigenetics
Clinical Epigenetics Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
8.90
自引率
5.30%
发文量
150
审稿时长
12 weeks
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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