Department of Hematology, University Medical Center Groningen, Groningen, The Netherland.
Blood. 2010 Nov 25;116(22):4621-30. doi: 10.1182/blood-2010-02-270660. Epub 2010 Aug 19.
The major limitation for the development of curative cancer therapies has been an incomplete understanding of the molecular mechanisms driving cancer progression. Human models to study the development and progression of chronic myeloid leukemia (CML) have not been established. Here, we show that BMI1 collaborates with BCR-ABL in inducing a fatal leukemia in nonobese diabetic/severe combined immunodeficiency mice transplanted with transduced human CD34(+) cells within 4-5 months. The leukemias were transplantable into secondary recipients with a shortened latency of 8-12 weeks. Clonal analysis revealed that similar clones initiated leukemia in primary and secondary mice. In vivo, transformation was biased toward a lymphoid blast crisis, and in vitro, myeloid as well as lymphoid long-term, self-renewing cultures could be established. Retroviral introduction of BMI1 in primary chronic-phase CD34(+) cells from CML patients elevated their proliferative capacity and self-renewal properties. Thus, our data identify BMI1 as a potential therapeutic target in CML.
治疗癌症方法发展的主要限制因素一直是对驱动癌症进展的分子机制的不完全了解。尚未建立用于研究慢性髓性白血病 (CML) 发展和进展的人类模型。在这里,我们表明 BMI1 与 BCR-ABL 合作,在 4-5 个月内将转导的人 CD34(+)细胞移植到非肥胖型糖尿病/严重联合免疫缺陷小鼠中,会导致致命性白血病。这些白血病可以在潜伏期为 8-12 周的二次受体内移植。克隆分析表明,相似的克隆在原发性和继发性小鼠中引发白血病。在体内,转化偏向于淋巴母细胞危象,并且可以在体外建立髓样和淋巴样长期自我更新培养物。逆转录病毒将 BMI1 引入 CML 患者的原发性慢性期 CD34(+)细胞中,提高了它们的增殖能力和自我更新特性。因此,我们的数据将 BMI1 确定为 CML 的潜在治疗靶点。