Institute of Chemical Biology, Henan University, Kaifeng, China.
Apoptosis. 2011 Jan;16(1):27-34. doi: 10.1007/s10495-010-0537-1.
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 IC(50). 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.
新型萘酰亚胺-聚胺缀合物 NPC-16 在 HepG2 细胞和 Bel-7402 细胞中的抗肿瘤作用及分子机制。通过 Annexin V-FITC 检测试剂盒评估细胞凋亡和坏死,通过吖啶橙和 Lyso-Tracker Red 染色评估自噬。使用罗丹明 123 染色测量线粒体跨膜电位的变化。通过免疫荧光分析和 Western blot 检测 Beclin 1、LC3 II 和 mTOR、p70S6K、14-3-3、caspase 以及 Bcl-2 家族成员的蛋白表达。在这里,我们阐明了 HepG2 细胞和 Bel-7402 细胞对 NPC-16 在 IC50 时的细胞反应性质。NPC-16 通过线粒体途径和死亡受体途径诱导 Bel-7402 细胞中 caspase 依赖性细胞凋亡。不同的是,NPC-16 触发 HepG2 细胞凋亡和自噬,进一步自噬促进细胞凋亡。此外,mTOR 信号通路参与 NPC-16 介导的 HepG2 细胞自噬。因此,NPC-16 可能是研究萘酰亚胺-聚胺缀合物抗肝癌分子机制的有用模板。