共 121 条
Single-cell genomics in AML: extending the frontiers of AML research
被引:36
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Gentles, Andrew J.
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Stanford Univ, Sch Med, Dept Biomed Data Sci, Stanford, CA 94305 USA Stanford Univ, Sch Med, Dept Med, Div Hematol, Stanford, CA 94305 USA

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机构:
[1] Stanford Univ, Sch Med, Dept Med, Div Hematol, Stanford, CA 94305 USA
[2] Stanford Univ, Canc Inst, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Biomed Data Sci, Stanford, CA 94305 USA
[5] Stanford Univ, Lokey Stem Cell Res Bldg,265 Campus Dr,G3021B,MC54, Stanford, CA 94305 USA
来源:
基金:
美国国家卫生研究院;
关键词:
ACUTE MYELOID-LEUKEMIA;
RESIDUAL DISEASE DETECTION;
WORLD-HEALTH-ORGANIZATION;
HEMATOPOIETIC STEM-CELLS;
ABILITY IN-VITRO;
PROGNOSTIC RELEVANCE;
CLASSIFICATION;
EXPRESSION;
REVEALS;
MUTATIONS;
D O I:
10.1182/blood.2021014670
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The era of genomic medicine has allowed acute myeloid leukemia (AML) researchers to improve disease characterization, optimize risk-stratification systems, and develop new treatments. Although there has been significant progress, AML remains a lethal cancer because of its remarkably complex and plastic cellular architecture. This degree of heterogeneity continues to pose a major challenge, because it limits the ability to identify and therefore eradicate the cells responsible for leukemogenesis and treatment failure. In recent years, the field of single-cell genomics has led to unprecedented strides in the ability to characterize cellular heterogeneity, and it holds promise for the study of AML. In this review, we highlight advancements in single-cell technologies, outline important shortcomings in our understanding of AML biology and clinical management, and discuss how single-cell genomics can address these shortcomings as well as provide unique opportunities in basic and translational AML research.
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页码:345 / 355
页数:11
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