Cytotoxic phenanthroline derivatives alter metallostasis and redox homeostasis in neuroblastoma cells.

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2018
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Abstract
Copper homeostasis is generally investigated focusing on a single component of the metallostasis network. Here we address several of the factors controlling the metallostasis for neuroblastoma cells (SH-SY5Y) upon treatment with 2,9-dimethyl-1,10-phenanthroline-5,6-dione (phendione) and 2,9-dimethyl-1,10-phenanthroline (cuproindione). These compounds bind and transport copper inside cells, exert their cytotoxic activity through the induction of oxidative stress, causing apoptosis and alteration of the cellular redox and copper homeostasis network. The intracellular pathway ensured by copper transporters (Ctr1, ATP7A), chaperones (CCS, ATOX, COX 17, Sco1, Sco2), small molecules (GSH) and transcription factors (p53) is scrutinised.
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naletova2018cytotoxic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Naletova, Irina;Satriano, Cristina;Curci, Alessandra;Margiotta, Nicola;Natile, Giovanni;Arena, Giuseppe;La Mendola, Diego;Nicoletti, Vincenzo Giuseppe;Rizzarelli, Enrico;
Journal oncotarget
Year 2018
DOI
10.18632/oncotarget.26346
URL
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