Jiang Xiaoyan, Smith Clayton, Eaves Allen, Eaves Connie
Terry Fox Laboratory, British Columbia Cancer Agency, Vancouver, Canada.
Clin Lymphoma Myeloma. 2007 Mar;7 Suppl 2:S71-80. doi: 10.3816/clm.2007.s.005.
Chronic myeloid leukemia (CML) is sustained by a clonally amplified population of Bcr Abl-positive pluripotent stem cells. Persistence of a large, functionally intact yet suppressed residual normal hematopoietic stem cell population in most patients with CML has made it possible to aim at the development of curative therapies. However, achieving this goal requires the identification of agents that will eradicate the leukemic stem cell population. Several potent Bcr-Abl-targeted drugs have now been introduced into clinical practice with remarkable effects. Nevertheless, accumulating data indicate that the leukemic CML stem cells in patients with chronic phase CML are less responsive to these agents than the bulk of the neoplastic cells. In this article, we review emerging evidence that CML stem cells have a number of unusual properties that underlie their relative insensitivity to treatment, including those that specifically target the Bcr-Abl oncoprotein. The biology of the neoplastic stem cells in patients with CML is clearly important to the future attainment of cures and might also prove a paradigm relevant to other types of malignancies that are sustained by transformed stem cell populations.
慢性髓性白血病(CML)由Bcr Abl阳性多能干细胞的克隆扩增群体维持。大多数CML患者中存在大量功能完整但受到抑制的残余正常造血干细胞群体,这使得开发治愈性疗法成为可能。然而,要实现这一目标,需要鉴定出能够根除白血病干细胞群体的药物。目前,几种有效的靶向Bcr-Abl的药物已被引入临床实践并取得了显著效果。尽管如此,越来越多的数据表明,慢性期CML患者的白血病CML干细胞对这些药物的反应比大部分肿瘤细胞更不敏感。在本文中,我们综述了新出现的证据,即CML干细胞具有许多不同寻常的特性,这些特性是其对治疗相对不敏感的基础,包括那些特异性靶向Bcr-Abl癌蛋白的特性。CML患者肿瘤干细胞的生物学特性对于未来实现治愈显然很重要,也可能成为与由转化干细胞群体维持的其他类型恶性肿瘤相关的范例。