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阻断细胞因子信号及强烈抑制 Bcr-Abl 激酶可诱导慢性髓系白血病祖细胞凋亡。

Blocking cytokine signaling along with intense Bcr-Abl kinase inhibition induces apoptosis in primary CML progenitors.

机构信息

Division of Haematology, SA Pathology, Adelaide, South Australia, Australia.

出版信息

Leukemia. 2010 Apr;24(4):771-8. doi: 10.1038/leu.2009.299. Epub 2010 Feb 4.

Abstract

In chronic myeloid leukemia (CML) cell lines, brief exposure to pharmacologically relevant dasatinib concentrations results in apoptosis. In this study, we assess the impact of intensity and duration of Bcr-Abl kinase inhibition on primary CD34(+) progenitors of chronic phase CML patients. As CML cells exposed to dasatinib in vivo are in a cytokine-rich environment, we also assessed the effect of cytokines (six growth factors cocktail or granulocyte-macrophage colony-stimulating factor (CSF) or granulocyte-CSF) in combination with dasatinib. In the presence of cytokines, short-term intense Bcr-Abl kinase inhibition (>or=90% p-Crkl inhibition) with 100 nM dasatinib did not reduce CD34(+) colony-forming cells (CFCs). In contrast, without cytokines, short-term exposure to dasatinib reduced CML-CD34(+) CFCs by 70-80%. When cytokines were added immediately after short-term exposure to dasatinib, CML-CD34(+) cells remained viable, suggesting that oncogene dependence of these cells can be overcome by concomitant or subsequent exposure to cytokines. Additional inhibition of Janus tyrosine kinase (Jak) activity re-established the sensitivity of CML progenitors to intense Bcr-Abl kinase inhibition despite the presence of cytokines. These findings support the contention that therapeutic strategies combining intense Bcr-Abl kinase inhibition and blockade of cytokine signaling pathways can be effective for eradication of CML progenitors.

摘要

在慢性髓性白血病 (CML) 细胞系中,短暂暴露于药理学相关的达沙替尼浓度可导致细胞凋亡。在这项研究中,我们评估了 Bcr-Abl 激酶抑制的强度和持续时间对慢性期 CML 患者原代 CD34+祖细胞的影响。由于体内暴露于达沙替尼的 CML 细胞处于细胞因子丰富的环境中,我们还评估了细胞因子(六种生长因子鸡尾酒或粒细胞-巨噬细胞集落刺激因子 (CSF) 或粒细胞-CSF)与达沙替尼联合使用的效果。在细胞因子存在的情况下,用 100 nM 达沙替尼进行短暂的高强度 Bcr-Abl 激酶抑制(>或=90%p-Crkl 抑制)并不会减少 CD34+集落形成细胞(CFC)。相比之下,在没有细胞因子的情况下,短暂暴露于达沙替尼可使 CML-CD34+CFC 减少 70-80%。当在短暂暴露于达沙替尼后立即添加细胞因子时,CML-CD34+细胞仍保持存活,表明这些细胞的致癌基因依赖性可以通过同时或随后暴露于细胞因子来克服。Janus 酪氨酸激酶 (Jak) 活性的额外抑制即使存在细胞因子,也能使 CML 祖细胞重新对高强度 Bcr-Abl 激酶抑制敏感。这些发现支持以下观点,即联合高强度 Bcr-Abl 激酶抑制和阻断细胞因子信号通路的治疗策略可有效根除 CML 祖细胞。

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