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YQ36: A Novel Bisindolylmaleimide Analogue Induces KB/VCR Cell Death

机译:YQ36:一种新颖的双吲哚基马来酰亚胺类似物诱导KB / VCR细胞死亡

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摘要

Overexpression of multidrug resistance proteins P-glycoprotein (P-gp, MDR1) causes resistance of the tumor cells against a variety of chemotherapeutic agents. 3-(1-methyl-1H-indol-3-yl)-1-phenyl-4-(1-(3-(piperidin-1-yl)propyl)-1H-pyrazolo[3,4-b]pyridine-3-yl)-1H-pyrrole-2,5-dione (YQ36) is a novel analogue of bisindolylmaleimide, which has been reported to overcome multidrug resistance. Here, we dedicated to investigate the anticancer activity of YQ36 on KB/VCR cells. The results revealed that YQ36 exhibited great antiproliferative activity on three parental cell lines and MDR1 overexpressed cell lines. Moreover, the hypersensitivity of YQ36 was confirmed on the base of great apoptosis induction and unaltered intracellular drug accumulation in KB/VCR cells. Further results suggested that YQ36 could not be considered as a substrate of P-gp, which contributed to its successfully escaping from the efflux mediated by P-gp. Interestingly, we observed that YQ36 could accumulate in nucleus and induce DNA damage. YQ36 could also induce the activation of caspase-3, imposing effects on the mitochondrial function. Collectively, our data demonstrated that YQ36 exhibited potent activities against MDR cells, inducing DNA damage and triggering subsequent apoptosis via mitochondrial pathway.
机译:多药耐药蛋白P-糖蛋白(P-gp,MDR1)的过表达导致肿瘤细胞对多种化学治疗剂产生耐药性。 3-(1-甲基-1H-吲哚-3-基)-1-苯基-4-(1-(3-(哌啶-1-基)丙基)-1H-吡唑并[3,4-b]吡啶- 3-yl)-1H-吡咯-2,5-二酮(YQ36)是双新吲哚基马来酰亚胺的新型类似物,据报道可克服多药耐药性。在这里,我们致力于研究YQ36对KB / VCR细胞的抗癌活性。结果表明,YQ36对三种亲本细胞系和MDR1过表达的细胞系均表现出极大的抗增殖活性。此外,在KB / VCR细胞中强烈的细胞凋亡诱导和细胞内药物蓄积未改变的基础上证实了YQ36的超敏性。进一步的结果表明,YQ36不能被视为P-gp的底物,这有助于其成功逃脱P-gp介导的外排。有趣的是,我们观察到YQ36可以在细胞核中积累并诱导DNA损伤。 YQ36还可以诱导caspase-3的活化,对线粒体功能产生影响。总的来说,我们的数据表明YQ36对MDR细胞表现出有效的活性,诱导DNA损伤并通过线粒体途径触发随后的细胞凋亡。

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