Circmsb Consorzio Interuniversitario Of Ric In Chimica Dei Metalli Nei Sistemi Biologici

Parma, Italy

Circmsb Consorzio Interuniversitario Of Ric In Chimica Dei Metalli Nei Sistemi Biologici

Parma, Italy
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Bisceglie F.,University of Parma | Bisceglie F.,Circmsb Consorzio Interuniversitario Of Ric In Chimica Dei Metalli Nei Sistemi Biologici | Pinelli S.,Circmsb Consorzio Interuniversitario Of Ric In Chimica Dei Metalli Nei Sistemi Biologici | Pinelli S.,University of Parma | And 10 more authors.
Journal of Inorganic Biochemistry | Year: 2014

This paper reports the synthesis and characterization of trans-cinnamaldehyde thiosemicarbazone (Htcin), cuminaldehyde thiosemicarbazone (Htcum) and their copper and nickel complexes. All the compounds, which on healthy cells (human fibroblasts) show a neglectable cytotoxicity, were screened in vitro in cell line U937 for their antileukemic activity. These compounds, in spite of their molecular similarity, present variegated behaviors. Htcin shows no inhibition activity in U935 cells, while both its metal complexes inhibit proliferation with IC50 at μM concentrations. The other ligand, Htcum, and its metal complexes, besides inhibiting proliferation, induce apoptosis. The cell cycle analysis highlights a G2/M checkpoint stop suggesting a possible direct action on DNA or on topoisomerase IIa. From CD and UV spectroscopy experiments, the DNA results to be not the main target of all these molecules, while both copper complexes are effective topoisomerase IIa inhibitors. All of these molecules activate caspase-9 and caspase-3, while caspase-8 activity is significantly induced by both cinnamaldehyde metal complexes. Tests on PgP and intracellular metal concentrations (determined by mean of atomic absorption spectrometry) show that the compounds tend to accumulate in the cytoplasm and that the cells do not manage to pump out copper and nickel ions. © 2014 Elsevier Inc.

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