Passegué Emmanuelle, Weisman Irving L
Stanford University School of Medicine, Pathology Department, Beckman Center B259, Stanford, CA 94305, USA.
Stem Cell Rev. 2005;1(3):181-8. doi: 10.1385/SCR:1:3:181.
Leukemias can now be viewed as aberrant hematopoietic processes initiated by rare cancer stem cells, or leukemic stem cells (LSCs) that have maintained or reacquired the capacity for indefinite proliferation through accumulated mutations and/or epigenetic changes. Yet, despite their critical importance, much remains to be learned about the developmental origin of LSCs and the mechanisms responsible for their emergence in the course of the disease. Mouse models of human leukemias have provided a unique system to study the mechanisms influencing LSC generation and function, and were recently used to demonstrate that LSCs can arise from both self-renewing hematopoietic stem cells (HSCs) and committed progenitor populations. This striking finding indicates that LSC identity is largely dictated by the nature of the oncogenic events and by how these events perturb essential processes such as self-renewal, proliferation, differentiation, and survival. Such approaches in the mouse are essential for the basic understanding of leukemogenesis and for the conceptual design of novel therapeutic strategies that could lead to improved treatments for human leukemias.
白血病现在可被视为由罕见的癌症干细胞,即白血病干细胞(LSC)引发的异常造血过程,这些干细胞通过累积突变和/或表观遗传变化维持或重新获得了无限增殖的能力。然而,尽管它们至关重要,但关于LSC的发育起源以及疾病过程中其出现的机制仍有许多有待了解之处。人类白血病的小鼠模型提供了一个独特的系统来研究影响LSC生成和功能的机制,最近被用于证明LSC可源自自我更新的造血干细胞(HSC)和定向祖细胞群体。这一惊人发现表明,LSC的特性在很大程度上由致癌事件的性质以及这些事件如何扰乱自我更新、增殖、分化和存活等基本过程所决定。小鼠中的此类研究方法对于白血病发生的基础理解以及可能改善人类白血病治疗的新型治疗策略的概念设计至关重要。