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Acute Myeloid Leukemia Stem Cells

机译:急性髓性白血病干细胞

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A fundamental problem in cancer research is identification of the cells within a tumor that sustain the growth of the neoplastic clone. The concept that only a subpopulation of rare cancer stem cells (CSCs) is responsible for maintenance of the neoplasm emerged nearly 50 years ago; however, conclusive proof for the existence of a CSC was obtained only relatively recently. The evidence for the existence of CSCs was first derived from the study of human acute myeloid leukemia (AML), largely because of the availability of quantitative stem cell assays for the leukemic stem cell (LSC). These studies showed that only rare cells within the leukemic clone had the capacity to initiate AML growth after transplant into NOD/SCID mice, establishing the hierarchical organization of AML. Recent clonal-tracking studies showed that the LSC compartment is composed of different classes of LSCs, which can be distinguished on the basis of self-renewal potential. These findings have important implications for our understanding of the leukemogenic process as well as the design of more effective therapies to eliminate AML based on eradication of the LSCs. These studies are briefly reviewed here.
机译:癌症研究中的一个基本问题是鉴定维持肿瘤克隆的生长的肿瘤内的细胞。只有稀有癌症干细胞(CSCs)亚群的概念是近50年前近50年前的肿瘤维持的概念;然而,最近仅获得了CSC的存在的结论证据。第一种源自对人急性髓性白血病(AML)的研究的存在证据,主要是因为白血病干细胞(LSC)的定量干细胞测定的可用性。这些研究表明,只有白血病克隆内的稀有细胞具有在移植到NOD / SCID小鼠移植到NOD / SCID小鼠后的AML生长的能力,建立了AML的分层组织。最近的克隆跟踪研究表明,LSC隔室由不同类别的LSC组成,其可以基于自我更新潜力来区分。这些发现对我们对白血动过程的理解以及更有效的疗法设计具有重要意义,以消除基于LSC的消除AML。这些研究在这里简要审查。

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