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NPC-16, a novel naphthalimide–polyamine conjugate, induced apoptosis and autophagy in human hepatoma HepG2 cells and Bel-7402 cells

机译:NPC-16是一种新型的萘二甲酰亚胺-多胺缀合物,可诱导人肝癌HepG2细胞和Bel-7402细胞凋亡和自噬

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The antitumor effects and molecular mechanism of NPC-16, a novel naphthalimide–polyamine conjugate, were evaluated in HepG2 cells and Bel-7402 cells. Apoptosis and necrosis were evaluated by Annexin V-FITC detection kit, and autophagy by acridine orange and Lyso-Tracker Red staining. The change of mitochondrial transmembrane potential was measured using rhodamine 123 staining. The protein expression of Beclin 1, LC3 II and mTOR, p70S6 K, 14-3-3, caspase, and Bcl-2 family members was detected by immunofluorescence assays and Western Blot. Here, we elucidated the nature of cellular response of HepG2 cells and Bel-7402 cells to NPC-16 at IC50. NPC-16 induced caspase-dependent apoptosis via the mitochondrial pathway and death receptor pathway in Bel-7402 cells. Differently, NPC-16 triggered HepG2 cells both apoptosis and autophagy, further autophagy facilitated cellular apoptosis. Furthermore, mTOR signal pathway was involved in NPC-16-mediated autophagy in HepG2 cells. Thus, NPC-16 may be useful as a potential template for investigation the molecular mechanism of naphthalimide–polyamine conjugate against hepatocellular carcinoma.
机译:在HepG2细胞和Bel-7402细胞中评估了一种新型的萘二甲酰亚胺-多胺缀合物NPC-16的抗肿瘤作用和分子机制。通过Annexin V-FITC检测试剂盒评估细胞凋亡和坏死,并通过a啶橙和Lyso-Tracker Red染色自噬。使用若丹明123染色测量线粒体跨膜电位的变化。通过免疫荧光测定和Western Blot检测Beclin 1,LC3 II和mTOR,p70S6 K,14-3-3,caspase和Bcl-2家族成员的蛋白表达。在这里,我们阐明了在IC 50 下HepG2细胞和Bel-7402细胞对NPC-16的细胞应答的性质。 NPC-16通过Bel-7402细胞中的线粒体途径和死亡受体途径诱导caspase依赖性凋亡。不同的是,NPC-16触发HepG2细胞凋亡和自噬,进一步的自噬促进细胞凋亡。此外,mTOR信号通路参与了NPC-16介导的HepG2细胞自噬。因此,NPC-16可用作研究萘二甲酰亚胺-多胺缀合物对抗肝细胞癌的分子机制的潜在模板。

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