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Synthesis and evaluation of pyridinium-hydrazone derivatives as potential antitumoral agents.

Abstract
The hydrazones of 4-hydrazinylpyridinium bearing alkylphenyl groups on pyridinium nitrogen were synthesized and evaluated for their cytotoxic activity against MCF-7, PC3, U2OS, and HEK293 cell lines by Wst1 cell proliferation assay. Cytotoxic activity results indicated that d derivatives having butylene chain; 4 and 5 series having naphthalene and anthracene ring systems showed high cytotoxic activity (IC50  = 3.27-8.54 μm) on cancer cells. 3d (4-(2-(4-hydroxybenzylidene)hydrazinyl)-1-(4-phenylbutyl)pyridinium bromide) was the most cytotoxic compound with IC50 value of 3.27 μm against MCF-7. The most active derivatives (1d, 2d, 3d, 4, and 5 series) were selected to investigate for the effects on autophagy by analyzing the expression of autophagy marker proteins. The conversion of LC3-I to its lipidated form LC3-II is essential for autophagy and related to autophagosomes. According to our results, all tested compounds except for 3d induced lipidated form LC3-II accumulation. Then, the effects of the compounds on p62 protein level were also analyzed by the immunoblotting as the autophagy inhibition results in accumulation of p62. Further molecular mechanistic studies including morphological analysis and live-death assays indicated that all tested compounds (1d, 2d, 3d, 4, and 5 series) are potent antitumoral molecules and all except for 3d have potential to inhibit autophagic flux.
AuthorsSülünay Parlar, Yalçın Erzurumlu, Recep Ilhan, Petek Ballar Kırmızıbayrak, Vildan Alptüzün, Ercin Erciyas
JournalChemical biology & drug design (Chem Biol Drug Des) Vol. 92 Issue 1 Pg. 1198-1205 (07 2018) ISSN: 1747-0285 [Electronic] England
PMID29415336 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2018 John Wiley & Sons A/S.
Chemical References
  • Antineoplastic Agents
  • Hydrazones
  • Microtubule-Associated Proteins
  • Pyridinium Compounds
  • Sequestosome-1 Protein
Topics
  • Antineoplastic Agents (chemical synthesis, chemistry, pharmacology)
  • Autophagy (drug effects)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Drug Screening Assays, Antitumor
  • HEK293 Cells
  • Humans
  • Hydrazones (chemical synthesis, chemistry, pharmacology)
  • Microtubule-Associated Proteins (metabolism)
  • Pyridinium Compounds (chemical synthesis, chemistry, pharmacology)
  • Sequestosome-1 Protein (metabolism)
  • Structure-Activity Relationship

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