Department of Cancer Biology, Beckman Research Institute, City of Hope, Duarte, CA, USA.
Blood. 2012 Feb 23;119(8):1904-14. doi: 10.1182/blood-2011-06-361691. Epub 2011 Dec 29.
The tyrosine kinase inhibitor imatinib is highly effective in the treatment of chronic myelogenous leukemia (CML), but primary and acquired resistance of CML cells to the drug offset its efficacy. Molecular mechanisms for resistance of CML to tyrosine kinase inhibitors are not fully understood. In the present study, we show that BCR-ABL activates the expression of the mammalian stress response gene SIRT1 in hematopoietic progenitor cells and that this involves STAT5 signaling. SIRT1 activation promotes CML cell survival and proliferation associated with deacetylation of multiple SIRT1 substrates, including FOXO1, p53, and Ku70. Imatinib-mediated inhibition of BCR-ABL kinase activity partially reduces SIRT1 expression and SIRT1 inhibition further sensitizes CML cells to imatinib-induced apoptosis. Knockout of SIRT1 suppresses BCR-ABL transformation of mouse BM cells and the development of a CML-like myeloproliferative disease, and treatment of mice with the SIRT1 inhibitor tenovin-6 deters disease progression. The combination of SIRT1 gene knockout and imatinib treatment further extends the survival of CML mice. Our results suggest that SIRT1 is a novel survival pathway activated by BCR-ABL expression in hematopoietic progenitor cells, which promotes oncogenic transformation and leukemogenesis. Our findings suggest further exploration of SIRT1 as a therapeutic target for CML treatment to overcome resistance.
酪氨酸激酶抑制剂伊马替尼在治疗慢性髓性白血病(CML)方面非常有效,但 CML 细胞对该药物的原发性和获得性耐药抵消了其疗效。CML 对酪氨酸激酶抑制剂耐药的分子机制尚未完全阐明。在本研究中,我们表明 BCR-ABL 在造血祖细胞中激活哺乳动物应激反应基因 SIRT1 的表达,这涉及 STAT5 信号通路。SIRT1 的激活促进 CML 细胞的存活和增殖,与包括 FOXO1、p53 和 Ku70 在内的多个 SIRT1 底物的去乙酰化有关。伊马替尼介导的 BCR-ABL 激酶活性抑制部分降低了 SIRT1 的表达,SIRT1 的抑制进一步使 CML 细胞对伊马替尼诱导的细胞凋亡敏感。SIRT1 的敲除抑制了 BCR-ABL 对小鼠 BM 细胞的转化和 CML 样骨髓增生性疾病的发展,SIRT1 抑制剂 tenovin-6 的治疗阻止了疾病的进展。SIRT1 基因敲除和伊马替尼治疗的联合进一步延长了 CML 小鼠的存活期。我们的研究结果表明,SIRT1 是一种在造血祖细胞中由 BCR-ABL 表达激活的新型存活途径,它促进了致癌转化和白血病的发生。我们的发现表明进一步探索 SIRT1 作为 CML 治疗的治疗靶点以克服耐药性。