驱动白血病干细胞自我更新的遗传和表观遗传改变。

Q4 Biochemistry, Genetics and Molecular Biology
Vincent van den Boom, Sarah J Horton, Jan Jacob Schuringa
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引用次数: 0

摘要

急性髓性白血病已成为癌症干细胞概念的典范。这一假说认为,这种疾病是由一群罕见的白血病起始干细胞维持的,这些干细胞已经获得了遗传或表观遗传的改变。很可能单个(epi)遗传事件不足以引起白血病,但需要一系列连续的事件。与正常的造血干细胞类似,来自骨髓生态位的内在和外在因素都为调节细胞命运决定提供了必要的线索,如白血病干细胞的自我更新和分化。在本章中,我们将回顾当前对白血病转化过程中遗传和表观遗传异常的理解,并将讨论哪些事件可能协同诱导白血病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic and epigenetic alterations that drive leukemic stem cell self-renewal.

Acute myeloid leukemia has emerged as a paradigm for the concept of the cancer stem cell. This hypothesis presumes that the disease is maintained by a rare population of leukemia-initiating stem cells which have acquired genetic or epigenetic changes. It is most likely that a single (epi)genetic event will not be sufficient to cause leukemia, but that a number of sequential events are required. Similar to normal hematopoietic stem cells, both intrinsic as well as extrinsic factors that arise from the bone marrow niche, provide essential cues that regulate cell fate decisions such as leukemic stem cell self-renewal and differentiation. In this chapter, we will review the current understanding of genetic and epigenetic abnormalities that underlie the process of leukemic transformation, and will discuss which events potentially co-operate to induce leukemia.

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来源期刊
Journal of Stem Cells
Journal of Stem Cells Medicine-Transplantation
CiteScore
0.10
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0.00%
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