METODO DI BELLA > PRINCIPI ATTIVI > Melatonina > Melatonin reduces pancreatic tumor cell viability by altering mitochondrial physiology.

 
Melatonin reduces pancreatic tumor cell viability by altering mitochondrial physiology. di Gonzalez A, Del Castillo-Vaquero A, Miro-Moran A, Tapia JA, Salido GM
 
 
Data: 08/04/2011
Tipologia: Area Pazienti - Documentazione
Lingua: Inglese
Pubblicazione: Journal of Pineal Research
Anno: 2011
Fonte: J Pineal Res. 2011 Apr;50(3):250-60.
 
 
Descrizione:

Melatonin reduces proliferation in many different cancer cell lines. Thus, melatonin is considered a promising antitumor agent, promoting apoptosis in tumor cells while preserving viability of normal cells. Herein, we examined the effects of melatonin on the pancreatic AR42J tumor cell line. We have analyzed cytosolic-free Ca(2+) concentration ([Ca(2+) ](c) ), mitochondrial-free Ca(2+) concentration ([Ca(2+) ](m) ), mitochondrial membrane potential (Ψm), mitochondrial flavin adenine dinucleotide (FAD) oxidative state, cellular viability and caspase-3 activity. Our results show that melatonin induced transient changes in [Ca(2+) ](c) and [Ca(2+) ](m) . Melatonin also induced depolarization of Ψm and led to a reduction in the level of oxidized FAD. In addition, melatonin reduced AR42J cell viability. Finally, we found a Ca(2+) -dependent caspase-3 activation in response to melatonin. Collectively, these data support the likelihood that melatonin reduces viability of tumor AR42J cells via its action on mitochondrial activity and caspase-3 activation.

 
 
 

 

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