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

      Apoptosis
      Acridine Orange, analysis, Annexin A5, Antimetabolites, Antineoplastic, chemical synthesis, pharmacology, Apoptosis, drug effects, Autophagy, Carcinoma, Hepatocellular, drug therapy, metabolism, pathology, Cell Line, Tumor, Cell Proliferation, Humans, Intracellular Signaling Peptides and Proteins, Liver Neoplasms, Membrane Potential, Mitochondrial, Mitochondria, Naphthalimides, chemistry, Necrosis, Polyamines, Receptors, Death Domain, Signal Transduction

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          Abstract

          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.

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