Wang Zhiqiang, Chen Ching-Cheng, Chen WenYong
Department of Cancer Biology, Beckman Research Institute, City of Hope, Duarte, California, USA.
Division of Hematopoietic Stem Cell and Leukemia Research, Beckman Research Institute, City of Hope, Duarte, California, USA.
Stem Cells. 2015 Dec;33(12):3437-51. doi: 10.1002/stem.2218. Epub 2015 Oct 15.
Leukemia stem cells (LSCs) of chronic myeloid leukemia (CML) are refractory to tyrosine kinase inhibitor treatment, persist in the residual disease, and are important source for disease recurrence. Better understanding CML LSCs will help devise new strategies to eradicate these cells. The BALB/c mouse model of CML using retroviral bone marrow transduction and transplantation is a widely used mouse model system for CML, but LSCs in this model are poorly characterized. Here, we show that lineage negative CD150(-) side population (CD150(-)SP), but not CD150(+)SP, are CML LSCs in this model, although both CD150(-)SP and CD150(+)SP cells are enriched for long-term hematopoietic stem cells in normal BALB/c mice. We previously showed that BCR-ABL transformation activates protein lysine deacetylase SIRT1 and inhibition of SIRT1 sensitizes CML stem/progenitor cells to tyrosine kinase inhibitors by acetylating and activating p53. In this study, we demonstrate that SIRT1 homozygous knockout substantially reduces CD150(-)SP CML LSCs, and compromises the maintenance of CML LSCs in the BALB/c model. We identified several molecular alterations in CD150(-)SP LSCs that included the elevated expression of cyclin-dependent kinase Cdk6 facilitating LSC activation and significantly reduced p53 expression. SIRT1 knockout suppressed Cdk6 expression and likely increases p53 protein functions through deacetylation without increasing its expression. Our results shed novel insight into CML LSCs and support a crucial role of SIRT1 in CML LSCs. Our study also provides a novel means for assessing new agents to eradicate CML LSCs.
慢性髓性白血病(CML)的白血病干细胞(LSCs)对酪氨酸激酶抑制剂治疗具有抗性,在残留疾病中持续存在,并且是疾病复发的重要来源。更好地了解CML LSCs将有助于设计根除这些细胞的新策略。使用逆转录病毒骨髓转导和移植的CML BALB/c小鼠模型是一种广泛用于CML的小鼠模型系统,但该模型中的LSCs特征不明确。在这里,我们表明,在该模型中,谱系阴性CD150(-)侧群细胞(CD150(-)SP)而非CD150(+)SP是CML LSCs,尽管在正常BALB/c小鼠中,CD150(-)SP和CD150(+)SP细胞都富含长期造血干细胞。我们之前表明,BCR-ABL转化激活蛋白赖氨酸脱乙酰酶SIRT1,抑制SIRT1可通过乙酰化和激活p53使CML干/祖细胞对酪氨酸激酶抑制剂敏感。在本研究中,我们证明SIRT1纯合敲除可显著减少CD150(-)SP CML LSCs,并损害BALB/c模型中CML LSCs的维持。我们在CD150(-)SP LSCs中鉴定了几种分子改变,包括细胞周期蛋白依赖性激酶Cdk6表达升高促进LSC激活以及p53表达显著降低。SIRT1敲除抑制Cdk6表达,并可能通过去乙酰化增加p53蛋白功能而不增加其表达。我们的结果为CML LSCs提供了新的见解,并支持SIRT1在CML LSCs中的关键作用。我们的研究还提供了一种评估根除CML LSCs新药物的新方法。