Literature DB >> 19576191

Cytotoxicity of methoctramine and methoctramine-related polyamines.

Maddalena Zini1, Catherine L Passariello, Davide Gottardi, Silvia Cetrullo, Flavio Flamigni, Carla Pignatti, Anna Minarini, Vincenzo Tumiatti, Andrea Milelli, Carlo Melchiorre, Claudio Stefanelli.   

Abstract

Methoctramine and its analogues are polymethylene tetramines that selectively bind to a variety of receptor sites. Although these compounds are widely used as pharmacological tools for receptor characterization, the toxicological properties of these polyamine-based structures are largely unknown. We have evaluated the cytotoxic effects of methoctramine and related symmetrical analogues differing in polymethylene chain length between the inner nitrogens against a panel of cell lines. Methoctramine caused cell death only at high micromolar concentrations, whereas its pharmacological action is exerted at nanomolar level. Increasing the spacing between the inner nitrogen atoms resulted in a significative increase in cytotoxicity. In particular, an elevated cytotoxicity is associated to a methylene chain length of 12 units dividing the inner amine functions (compound 5). H9c2 cardiomyoblasts were the most sensitive cells, followed by SH-SY5Y neuroblastoma, whereas HL60 leukaemia cells were much more resistant. Methoctramine and related compounds down-regulated ornithine decarboxylase, the first enzyme of polyamine biosynthesis even at non-toxic concentration. Further, methoctramine and compound 5 caused a limited up-regulation of spermine/spermidine N-acetyltransferase, suggesting that interference in polyamine metabolism is not a primary mechanism of toxicity. Methoctramine and its analogues bound to DNA with a higher affinity than spermine, but the correlation with their toxic effect was poor. The highly toxic compound 5 killed the cells in the absence of caspase activation and caused an increase in p53 expression and ERK1/2 phosphorylation. Compound 5 was directly oxidized by cell homogenates producing hydrogen peroxide and its toxic effect was partially subdued by the inhibition of its uptake, by the NMDA ligand MK-801, and by the antioxidant N-acetylcysteine, suggesting that compound 5 can act at different cellular levels and lead to oxidative stress.

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Year:  2009        PMID: 19576191     DOI: 10.1016/j.cbi.2009.06.015

Source DB:  PubMed          Journal:  Chem Biol Interact        ISSN: 0009-2797            Impact factor:   5.192


  4 in total

1.  Substituted E-3-(3-indolylmethylene)-1,3-dihydroindol-2-ones with antitumor activity. In depth study of the effect on growth of breast cancer cells.

Authors:  Aldo Andreani; Stefania Bellini; Silvia Burnelli; Massimiliano Granaiola; Alberto Leoni; Alessandra Locatelli; Rita Morigi; Mirella Rambaldi; Lucilla Varoli; Natalia Calonghi; Concettina Cappadone; Maddalena Zini; Claudio Stefanelli; Lanfranco Masotti; Robert H Shoemaker
Journal:  J Med Chem       Date:  2010-08-12       Impact factor: 7.446

2.  Network-based assessment of the selectivity of metabolic drug targets in Plasmodium falciparum with respect to human liver metabolism.

Authors:  Susanna Bazzani; Andreas Hoppe; Hermann-Georg Holzhütter
Journal:  BMC Syst Biol       Date:  2012-08-31

3.  Identification of Deregulated Signaling Pathways in Jurkat Cells in Response to a Novel Acylspermidine Analogue-N4-Erucoyl Spermidine.

Authors:  Syed Shoeb Razvi; Hani Choudhry; Mohammed Nihal Hasan; Mohammed A Hassan; Said Salama Moselhy; Khalid Omer Abualnaja; Mazin A Zamzami; Taha Abduallah Kumosani; Abdulrahman Labeed Al-Malki; Majed A Halwani; Abdulkhaleg Ibrahim; Ali Hamiche; Christian Bronner; Tadao Asami; Mahmoud Alhosin
Journal:  Epigenet Insights       Date:  2018-11-27

4.  Identification and Characterization of Novel Small-Molecule SMOX Inhibitors.

Authors:  Amelia B Furbish; Ahmed S Alford; Pieter Burger; Yuri K Peterson; Tracy Murray-Stewart; Robert A Casero; Patrick M Woster
Journal:  Med Sci (Basel)       Date:  2022-08-30
  4 in total

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