Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, No. 250, Wuxing St., Taipei, 11031, Taiwan.
School of Pharmacy, College of Pharmacy, Taipei Medical University, No. 250, Wuxing St., Taipei, 11031, Taiwan.
Invest New Drugs. 2017 Aug;35(4):427-435. doi: 10.1007/s10637-017-0457-9. Epub 2017 Mar 27.
Chronic myeloid leukemia (CML) is a hematopoietic malignancy caused by the constitutive activation of Bcr-Abl tyrosine kinase. The Bcr-Abl inhibitor imatinib and other second-generation tyrosine kinase inhibitors such as dasatinib and nilotinib have remarkable efficacy in CML treatment. However, gene mutation-mediated drug resistance remains a critical problem. Among point mutations, the Bcr-Abl T315I mutation confers resistance to these Bcr-Abl inhibitors. Previously, we have synthesized the compound (1-methyl-1H-indol-5-yl)-(3,4,5-trimethoxy-phenyl)-methanone (MPT0B002) as a novel microtubule inhibitor. In this study, we evaluated its effects on the proliferation, cell cycle, and apoptosis of K562 CML cells and BaF3 cells expressing either wild-type Bcr-Abl (BaF3/p210) or T315I-mutated Bcr-Abl (BaF3/T315I). MPT0B002 inhibited cell viability in a dose-dependent manner in these cells but did not affect the proliferation of human umbilical vein endothelial cells. It disrupted tubulin polymerization and arrested cell cycle at the G2/M phase. Treatment with MPT0B002 induced apoptosis, and this induction was associated with increased levels of cleaved caspase-3 and cleaved PARP. Furthermore, MPT0B002 can downregulate both Bcr-Abl and Bcr-Abl-T315I mRNA expressions and protein levels and the downstream signaling pathways. Taken together, our findings suggest that MPT0B002 may be considered a promising compound to downregulate not only wild type Bcr-Abl but also the T315I mutant to overcome Bcr-Abl-T315I mutation-mediated resistance in CML cells.
慢性髓性白血病(CML)是一种造血系统恶性肿瘤,由 Bcr-Abl 酪氨酸激酶的组成性激活引起。Bcr-Abl 抑制剂伊马替尼和其他第二代酪氨酸激酶抑制剂,如达沙替尼和尼洛替尼,在 CML 治疗中具有显著疗效。然而,基因突变更药耐药仍然是一个关键问题。在点突变中,Bcr-Abl T315I 突变赋予了这些 Bcr-Abl 抑制剂的耐药性。以前,我们合成了一种化合物(1-甲基-1H-吲哚-5-基)-(3,4,5-三甲氧基-苯基)-甲酮(MPT0B002),作为一种新型的微管抑制剂。在这项研究中,我们评估了它对表达野生型 Bcr-Abl(BaF3/p210)或 T315I 突变型 Bcr-Abl(BaF3/T315I)的 K562 CML 细胞和 BaF3 细胞增殖、细胞周期和凋亡的影响。MPT0B002 以剂量依赖的方式抑制这些细胞的活力,但不影响人脐静脉内皮细胞的增殖。它破坏微管聚合并将细胞周期阻滞在 G2/M 期。用 MPT0B002 处理诱导细胞凋亡,这种诱导与 cleaved caspase-3 和 cleaved PARP 水平的增加有关。此外,MPT0B002 可以下调 Bcr-Abl 和 Bcr-Abl-T315I 的 mRNA 表达和蛋白水平及其下游信号通路。综上所述,我们的研究结果表明,MPT0B002 可能被认为是一种有前途的化合物,不仅可以下调野生型 Bcr-Abl,还可以下调 T315I 突变体,以克服 CML 细胞中 Bcr-Abl-T315I 突变介导的耐药性。