Volume 50, Issue 2 p. 150-158

Melatonin and vitamin D3 synergistically down-regulate Akt and MDM2 leading to TGFβ-1-dependent growth inhibition of breast cancer cells

Sara Proietti,

Department of Experimental Medicine, University “La Sapienza”, Roma, Italy

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Alessandra Cucina,

Department of Surgery “P.Valdoni”, University “La Sapienza”, Roma, Italy

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Fabrizio D’Anselmi,

Department of Surgery “P.Valdoni”, University “La Sapienza”, Roma, Italy

ASI, Italian Space Agency, Rome, Italy

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Simona Dinicola,

Department of Experimental Medicine, University “La Sapienza”, Roma, Italy

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Alessia Pasqualato,

Department of Basic and Applied Medical Sciences, University G. d’Annunzio, Chieti-Pescara, Italy

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Elisabetta Lisi,

Department of Biology, University of “Roma Tre”, Roma, Italy

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Mariano Bizzarri,

Department of Experimental Medicine, University “La Sapienza”, Roma, Italy

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First published: 22 November 2010
Citations: 17
Address reprint request to Mariano Bizzarri, 14-16, Via Antonio Scarpa, Roma 00161, Italy.
E-mail: mariano.bizzarri@uniroma1.it

Abstract

Abstract: Melatonin and vitamin D3 inhibit breast cancer cell growth and induce apoptosis, but they have never been combined as a breast cancer treatment. Therefore, we investigated whether their association could lead to an enhanced anticancer activity. In MCF-7 breast cancer cells, melatonin together with vitamin D3, induced a synergistic proliferative inhibition, with an almost complete cell growth arrest at 144 hr. Cell growth blockade is associated to an activation of the TGFβ-1 pathway, leading to increased TGFβ-1, Smad4 and phosphorylated-Smad3 levels. Concomitantly, melatonin and D3, alone or in combination, caused a significant reduction in Akt phosphorylation and MDM2 values, with a consequent increase of p53/MDM2 ratio. These effects were completely suppressed by adding a monoclonal anti-TGFβ-1 antibody to the culture medium. Taken together, these results indicate that cytostatic effects triggered by melatonin and D3 are likely related to a complex TGFβ-1-dependent mechanism, involving down-regulation of both MDM2 and Akt-phosphorylation.

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