1] INSERM, U848, Villejuif, France [2] Institut Gustave Roussy, Villejuif, France [3] Université Paris Sud/Paris XI, Le Kremlin Bicêtre, France [4] CNRS, UMR 5237, Montpellier, France.
Cell Death Differ. 2013 Nov;20(11):1532-45. doi: 10.1038/cdd.2013.105. Epub 2013 Aug 9.
Monopolar spindle 1 (MPS1), a mitotic kinase that is overexpressed in several human cancers, contributes to the alignment of chromosomes to the metaphase plate as well as to the execution of the spindle assembly checkpoint (SAC). Here, we report the identification and functional characterization of three novel inhibitors of MPS1 of two independent structural classes, N-(4-{2-[(2-cyanophenyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}phenyl)-2-phenylacetamide (Mps-BAY1) (a triazolopyridine), N-cyclopropyl-4-{8-[(2-methylpropyl)amino]-6-(quinolin-5-yl)imidazo[1,2-a]pyrazin-3-yl}benzamide (Mps-BAY2a) and N-cyclopropyl-4-{8-(isobutylamino)imidazo[1,2-a]pyrazin-3-yl}benzamide (Mps-BAY2b) (two imidazopyrazines). By selectively inactivating MPS1, these small inhibitors can arrest the proliferation of cancer cells, causing their polyploidization and/or their demise. Cancer cells treated with Mps-BAY1 or Mps-BAY2a manifested multiple signs of mitotic perturbation including inefficient chromosomal congression during metaphase, unscheduled SAC inactivation and severe anaphase defects. Videomicroscopic cell fate profiling of histone 2B-green fluorescent protein-expressing cells revealed the capacity of MPS1 inhibitors to subvert the correct timing of mitosis as they induce a premature anaphase entry in the context of misaligned metaphase plates. Hence, in the presence of MPS1 inhibitors, cells either divided in a bipolar (but often asymmetric) manner or entered one or more rounds of abortive mitoses, generating gross aneuploidy and polyploidy, respectively. In both cases, cells ultimately succumbed to the mitotic catastrophe-induced activation of the mitochondrial pathway of apoptosis. Of note, low doses of MPS1 inhibitors and paclitaxel (a microtubular poison) synergized at increasing the frequency of chromosome misalignments and missegregations in the context of SAC inactivation. This resulted in massive polyploidization followed by the activation of mitotic catastrophe. A synergistic interaction between paclitaxel and MPS1 inhibitors could also be demonstrated in vivo, as the combination of these agents efficiently reduced the growth of tumor xenografts and exerted superior antineoplastic effects compared with either compound employed alone. Altogether, these results suggest that MPS1 inhibitors may exert robust anticancer activity, either as standalone therapeutic interventions or combined with microtubule-targeting chemicals.
单极纺锤体 1(MPS1)是一种在多种人类癌症中过度表达的有丝分裂激酶,它有助于染色体向中期板的排列以及纺锤体组装检查点(SAC)的执行。在这里,我们报告了两种独立结构类别的三种新型 MPS1 抑制剂的鉴定和功能表征,N-(4-{2-[(2-氰基苯基)氨基][1,2,4]三唑[1,5-a]吡啶-6-基}苯基)-2-苯基乙酰胺(Mps-BAY1)(三唑并吡啶),N-环丙基-4-{8-[(2-甲基丙基)氨基]-6-(喹啉-5-基)咪唑并[1,2-a]吡嗪-3-基}苯甲酰胺(Mps-BAY2a)和 N-环丙基-4-{8-(异丁基氨基)咪唑并[1,2-a]吡嗪-3-基}苯甲酰胺(Mps-BAY2b)(两个咪唑并吡嗪)。这些小分子抑制剂通过选择性失活 MPS1,可以阻止癌细胞的增殖,导致它们的多倍体化和/或死亡。用 Mps-BAY1 或 Mps-BAY2a 处理的癌细胞表现出有丝分裂扰动的多种迹象,包括中期染色体的无效趋同,不合时宜的 SAC 失活和严重的后期缺陷。表达组蛋白 2B-绿色荧光蛋白的细胞的视频显微镜细胞命运分析揭示了 MPS1 抑制剂改变有丝分裂正确时间的能力,因为它们在中期板错位的情况下诱导过早的后期进入。因此,在 MPS1 抑制剂存在的情况下,细胞要么以双极(但通常不对称)方式分裂,要么进入一个或多个有丝分裂失败的轮次,分别产生巨大的非整倍体和多倍体。在这两种情况下,细胞最终都会因有丝分裂灾难诱导的线粒体凋亡途径的激活而死亡。值得注意的是,低剂量的 MPS1 抑制剂和紫杉醇(一种微管毒物)协同作用,增加了 SAC 失活时染色体错位和分离的频率。这导致大量的多倍体化,随后激活有丝分裂灾难。紫杉醇和 MPS1 抑制剂之间的协同相互作用也可以在体内得到证明,因为这些药物的组合有效地减少了肿瘤异种移植物的生长,并与单独使用任何一种化合物相比,发挥了更好的抗肿瘤作用。总之,这些结果表明,MPS1 抑制剂可能具有强大的抗癌活性,无论是作为独立的治疗干预措施,还是与微管靶向化学物质联合使用。