http://www.cnr.it/ontology/cnr/individuo/prodotto/ID179353
Mitochondria are primary targets in apoptosis induced by the mixed phosphine gold species chlorotriphenylphosphine-1,3-bis(diphenylphosphino)propanegold(I) in melanoma cell lines. (Articolo in rivista)
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- Mitochondria are primary targets in apoptosis induced by the mixed phosphine gold species chlorotriphenylphosphine-1,3-bis(diphenylphosphino)propanegold(I) in melanoma cell lines. (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.bcp.2006.11.018 (literal)
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CARUSO Francesco; VILLA Raffaella; ROSSI Miriam; PETTINARI Claudio; PADUANO Francesco; PENNATI Marzia; DAIDONE Maria Grazia; ZAFFARONI, Nadia (2007)
Mitochondria are primary targets in apoptosis induced by the mixed phosphine gold species chlorotriphenylphosphine-1,3-bis(diphenylphosphino)propanegold(I) in melanoma cell lines.
in Biochemical pharmacology
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- CARUSO Francesco; VILLA Raffaella; ROSSI Miriam; PETTINARI Claudio; PADUANO Francesco; PENNATI Marzia; DAIDONE Maria Grazia; ZAFFARONI, Nadia (literal)
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- http://dx.doi.org/10.1016/j.bcp.2006.11.018 (literal)
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- Istituto di Chimica Biomolecolare, Consiglio Nazionale delle Ricerche, Piazzale Aldo Moro 5, 00185 Rome, Italy;
Dipartimento di Oncologia Sperimentale e Laboratori, Fondazione IRCCS Istituto Nazionale dei Tumori,
Via Venezian 1, 20133 Milan, Italy;
Vassar College, Department of Chemistry, Poughkeepsie, NY 12604-0484, USA;
Dipartimento di Scienze Chimiche, Universita di Camerino, via S. Agostino 1, 62032 Camerino, MC, Italy (literal)
- Titolo
- Mitochondria are primary targets in apoptosis induced by the mixed phosphine gold species chlorotriphenylphosphine-1,3-bis(diphenylphosphino)propanegold(I) in melanoma cell lines. (literal)
- Abstract
- Based on previous evidence indicating a selective cytotoxic activity of the mixed phosphine
gold complex chlorotriphenylphosphine-1,3-bis(diphenylphosphino)propanegold(I) for
melanoma cells, we investigated the cellular bases of its antiproliferative effect in a panel
of human melanoma cell lines (JR8, SK-Mel-5, Mel-501, 2/60, 2/21 and GRIG). The drug
consistently induced a dose-dependent inhibition of cell growth, with IC50 values ranging
from 0.8 to 2.3 mM and, when tested under the same experimental conditions, its cytotoxic
activity was higher than (from 2- to 5-fold) or comparable to that of cisplatin as a function of
cell lines. The ability of the gold complex to activate programmed cell death was assessed in
JR8 and 2/60 cells, and a dose-dependent increase in cells with an apoptotic nuclear
morphology was observed in both cell lines (up to 40 and 66% of the overall cell population,
for JR8 and 2/60 cell lines, respectively). Such an apoptotic response was mediated by a dosedependent
loss of mitochondrial membrane potential, cytochrome c and Smac/DIABLO
release from mitochondria into cytosol and enhanced caspase-9 and caspase-3 catalytic
activity. A reduced or completely abrogated expression of the anti-apoptotic proteins c-IAP1,
XIAP and survivin in drug-treated cells was also observed. Overall, results from the study
indicate that chlorotriphenylphosphine-1,3-bis(diphenylphosphino)propanegold(I) markedly
inhibits melanoma cell growth by inducing mitochondria-mediated apoptosis and
suggest it as a good candidate for additional evaluation as an anticancer agent against
melanoma. (literal)
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