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新型 Aurora A 激酶抑制剂 MLN8237 对耐药性慢性髓性白血病有效,并显著提高了尼洛替尼的疗效。

The novel Aurora A kinase inhibitor MLN8237 is active in resistant chronic myeloid leukaemia and significantly increases the efficacy of nilotinib.

机构信息

Department of Medicine, Cancer Therapy and Research Center at The University of Texas Health Science Center at San Antonio, San Antonio, TX 78245, USA.

出版信息

J Cell Mol Med. 2011 Oct;15(10):2057-70. doi: 10.1111/j.1582-4934.2010.01218.x.

Abstract

Novel therapies are urgently needed to prevent and treat tyrosine kinase inhibitor resistance in chronic myeloid leukaemia (CML). MLN8237 is a novel Aurora A kinase inhibitor under investigation in multiple phase I and II studies. Here we report that MLN8237 possessed equipotent activity against Ba/F3 cells and primary CML cells expressing unmutated and mutated forms of breakpoint cluster region-Abelson kinase (BCR-ABL). Notably, this agent retained high activity against the T315I and E255K BCR-ABL mutations, which confer the greatest degree of resistance to standard therapy. MLN8237 treatment disrupted cell cycle kinetics, induced apoptosis, caused a dose-dependent reduction in the expression of the large inhibitor of apoptosis protein Apollon, and produced a morphological phenotype consistent with Aurora A kinase inhibition. In contrast to other Aurora kinase inhibitors, MLN8237 did not significantly affect BCR-ABL activity. Moreover, inhibition of Aurora A with MLN8237 significantly increased the in vitro and in vivo efficacy of nilotinib. Targeted knockdown of Apollon sensitized CML cells to nilotinib-induced apoptosis, indicating that this is an important factor underlying MLN8237's ability to increase the efficacy of nilotinib. Our collective data demonstrate that this combination strategy represents a novel therapeutic approach for refractory CML that has the potential to suppress the emergence of T315I mutated CML clones.

摘要

迫切需要新的疗法来预防和治疗慢性髓性白血病(CML)中的酪氨酸激酶抑制剂耐药性。MLN8237 是一种新型的 Aurora A 激酶抑制剂,正在多项 I 期和 II 期研究中进行研究。在这里,我们报告 MLN8237 对表达未突变和突变形式的断点簇区域-Abelson 激酶(BCR-ABL)的 Ba/F3 细胞和原代 CML 细胞具有等效的活性。值得注意的是,该药物对 T315I 和 E255K BCR-ABL 突变仍保持高活性,这些突变赋予了对标准治疗的最大程度的耐药性。MLN8237 治疗破坏了细胞周期动力学,诱导了细胞凋亡,导致凋亡抑制蛋白 Apollon 的表达剂量依赖性降低,并产生了与 Aurora A 激酶抑制一致的形态表型。与其他 Aurora 激酶抑制剂不同,MLN8237 对 BCR-ABL 活性没有显著影响。此外,用 MLN8237 抑制 Aurora A 显著提高了 nilotinib 的体外和体内疗效。靶向敲低 Apollon 使 CML 细胞对 nilotinib 诱导的凋亡敏感,表明这是 MLN8237 增加 nilotinib 疗效的重要因素。我们的综合数据表明,这种联合策略代表了一种治疗难治性 CML 的新方法,有可能抑制 T315I 突变 CML 克隆的出现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbd0/4394217/195862ef18c3/jcmm0015-2057-f1.jpg

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