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Synthesis of a novel adamantyl nitroxide derivative with potent anti-hepatoma activity in vitro and in vivo

机译:体内和体外具有抗肝癌活性的新型金刚烷氮氧化物衍生物的合成

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摘要

In this study, a novel adamantyl nitroxide derivative was synthesized and its antitumor activities in vitro and in vivo were investigated. The adamantyl nitroxide derivative >4 displayed a potent anticancer activity against all the tested human hepatoma cells, especially with IC50 of 68.1 μM in Bel-7404 cells, compared to the positive control 5-FU (IC50=607.7 μM). The significant inhibition of cell growth was also observed in xenograft mouse model, with low toxicity. Compound >4 suppressed the cell migration and invasion, induced the G2/M phase arrest. Further mechanistic studies revealed that compound >4 induced cell death, which was accompanied with damaging mitochondria, increasing the generation of intracellular reactive oxygen species, cleavages of caspase-9 and caspase-3, as well as activations of Bax and Bcl-2. These results confirmed that adamantyl nitroxide derivative exhibited selective antitumor activities via mitochondrial apoptosis pathway in Bel-7404 cells, and would be a potential anticancer agent for liver cancer.
机译:在这项研究中,合成了一种新型的金刚烷氮氧化物衍生物,并研究了其在体内外的抗肿瘤活性。与阳性对照5-FU(IC50 = 607.7μM)相比,金刚烷氮氧化物衍生物> 4 显示出对所有测试的人肝癌细胞有效的抗癌活性,尤其是Bel-7404细胞的IC50为68.1μM。 )。在异种移植小鼠模型中也观察到细胞生长的显着抑制,毒性低。化合物> 4 抑制细胞迁移和侵袭,诱导G2 / M期阻滞。进一步的机理研究表明,化合物> 4 诱导细胞死亡,并伴随线粒体破坏,增加细胞内活性氧的生成,caspase-9和caspase-3的裂解以及Bax的激活。和Bcl-2。这些结果证实,金刚烷氮氧化物衍生物通过Bel-7404细胞中的线粒体凋亡途径表现出选择性的抗肿瘤活性,并且将是潜在的肝癌抗癌剂。

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