Genomics of AML: Clinical Applications of Next-Generation Sequencing

被引:31
作者
Welch, John S. [1 ]
Link, Daniel C. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Med, Div Oncol, St Louis, MO 63110 USA
关键词
ACUTE MYELOID-LEUKEMIA; MUTATIONS; PREDISPOSITION; CANCERS; DNMT3A;
D O I
10.1182/asheducation-2011.1.30
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
In the past decade, a series of technological advances have revolutionized our ability to interrogate cancer genomes, culminating in whole-genome sequencing, which provides genome-wide coverage at a single base-pair resolution. As sequencing technologies improve and costs decrease, it is likely that whole-genome sequencing of cancer cells will become commonplace in the diagnostic workup of patients with acute myelogenous leukemia (AML) and other cancers. The unprecedented molecular characterization provided by whole-genome sequencing offers the potential for an individualized approach to treatment in AML, bringing us one step closer to personalized medicine. In this chapter, we discuss how next-generation sequencing is being used to study cancer genomes. Recent publications of whole-genome sequencing in AML are reviewed and current limitations of whole-genome sequencing are examined, as well as current and potential future clinical applications of whole-genome sequencing.
引用
收藏
页码:30 / 35
页数:6
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