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Mechanisms underlying 3-bromopyruvate-induced cell death in colon cancer

机译:3-溴丙酮酸盐诱导结肠癌细胞死亡的潜在机制

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摘要

3-Bromopyruvate (3BP) is an energy-depleting drug that inhibits Hexokinase II activity by alkylation during glycolysis, thereby suppressing the production of ATP and inducing cell death. As such, 3BP can potentially serve as an anti-tumorigenic agent. Our previous research showed that 3BP can induce apoptosis via AKT /protein Kinase B signaling in breast cancer cells. Here we found that 3BP can also induce colon cancer cell death by necroptosis and apoptosis at the same time and concentration in the SW480 and HT29 cell lines; in the latter, autophagy was also found to be a mechanism of cell death. In HT29 cells, combined treatment with 3BP and the autophagy inhibitor 3-methyladenine (3-MA) exacerbated cell death, while viability in 3BP-treated cells was enhanced by concomitant treatment with the caspase inhibitor benzyloxycarbonyl-Val-Ala-Asp fluoromethylketone (z-VAD-fmk) and the necroptosis inhibitor necrostatin (Nec)-1. Moreover, 3BP inhibited tumor growth in a SW480 xenograft mouse model. These results indicate that 3BP can suppress tumor growth and induce cell death by multiple mechanisms at the same time and concentration in different types of colon cancer cell by depleting cellular energy stores.
机译:3-溴丙酮酸(3BP)是一种耗能药物,可在糖酵解过程中通过烷基化抑制己糖激酶II的活性,从而抑制ATP的产生并诱导细胞死亡。这样,3BP可以潜在地用作抗致瘤剂。我们以前的研究表明3BP可通过AKT /蛋白激酶B信号传导诱导乳腺癌细胞凋亡。在这里,我们发现3BP还可以同时通过SW480和HT29细胞系中的坏死和凋亡诱导结肠癌细胞死亡。在后者中,自噬也是细胞死亡的机制。在HT29细胞中,与3BP和自噬抑制剂3-甲基腺嘌呤(3-MA)联合处理可加剧细胞死亡,而同时通过半胱天冬酶抑制剂苄氧基羰基-Val-Ala-Asp氟甲基酮处理可增强3BP处理的细胞的活力(z -VAD-fmk)和坏死抑制剂necrostatin(Nec)-1。此外,在SW480异种移植小鼠模型中3BP抑制了肿瘤的生长。这些结果表明3BP可以通过多种机制同时抑制肿瘤生长并诱导细胞死亡,并且通过消耗细胞能量储存在不同类型的结肠癌细胞中浓缩。

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