Department of Pediatrics and Adolescent Medicine, Ulm University, Ulm, Germany. lueder–hinrich.meyer@uniklinik–ulm.de
Cancer Res. 2011 Dec 1;71(23):7141-4. doi: 10.1158/0008-5472.CAN-11-1732. Epub 2011 Nov 16.
Over the past decade, xenografting human leukemia cells into mice with different levels of immunodeficiency, with or without preconditioning, has provided an important tool to study various aspects of leukemia biology and to identify distinct clinical risk groups for evaluation of novel therapeutic strategies, as well as the possibility of amplifying human leukemia cells in vivo. Interestingly, these models using human acute lymphoblastic leukemia and acute myeloid leukemia cells as xenografts recapitulate many clinical features of the disease. Similar to the human environment (for example, in the bone marrow), transplanted leukemia cells in the murine setting are exposed to both favorable and unfavorable conditions for engraftment that may exert a distinct pressure for selection of subclones. Thus, results obtained in these models may vary depending on the experimental setup. The impact of in vivo growth of human leukemia cells on the background of a more or less hostile murine environment for leukemia biology and the course of the disease in patients are discussed in the context of the diversity of xenograft models.
在过去的十年中,通过将不同免疫缺陷程度的人类白血病细胞异种移植到小鼠体内,并进行或不进行预处理,为研究白血病生物学的各个方面以及确定用于评估新型治疗策略的不同临床风险组提供了重要工具,也为在体内扩增人类白血病细胞提供了可能。有趣的是,这些使用人急性淋巴细胞白血病和急性髓细胞白血病细胞作为异种移植物的模型再现了该疾病的许多临床特征。与人类环境相似(例如,在骨髓中),移植到小鼠体内的白血病细胞会受到有利于和不利于植入的各种条件的影响,这可能会对亚克隆的选择施加不同的压力。因此,这些模型中获得的结果可能会因实验设置的不同而有所差异。本文将讨论在不同的异种移植模型背景下,人类白血病细胞在体内生长对白血病生物学和患者疾病进程的影响。