Synthesis and in-depth studies on the anticancer activity of novel palladacyclopentadienyl complexes stabilized by N-Heterocyclic carbene ligands
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Scattolin, Thomas
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Caligiuri, Isabella
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Mouawad, Nayla
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El Boustani, Maguie
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IRCCS CRO Aviano Natl Canc Inst, Pathol Unit, I-33081 Aviano, ItalyUniv Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci Via Torino 155, I-30174 Venice, Italy
El Boustani, Maguie
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Demitri, Nicola
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Elettra Sincrotrone Trieste, SS 14 Km 163-5 Area Sci Pk, I-34149 Trieste, ItalyUniv Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci Via Torino 155, I-30174 Venice, Italy
Demitri, Nicola
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Rizzolio, Flavio
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Univ Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci Via Torino 155, I-30174 Venice, Italy
IRCCS CRO Aviano Natl Canc Inst, Pathol Unit, I-33081 Aviano, ItalyUniv Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci Via Torino 155, I-30174 Venice, Italy
Rizzolio, Flavio
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Visentin, Fabiano
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Univ Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci Via Torino 155, I-30174 Venice, ItalyUniv Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci Via Torino 155, I-30174 Venice, Italy
Visentin, Fabiano
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[1] Univ Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci Via Torino 155, I-30174 Venice, Italy
New palladacyclopentadienyl complexes with bis-N-heterocyclic carbenes as spectator ligands have been synthesized and exhaustively characterized. The crystal structure of complex la has been also determined by X-ray diffraction analysis. Their in vitro cytotoxicity and that of other palladacyclopentadienyl derivatives coordinating different ancillary ligands has been determined against different cancer cell lines. Many complexes have shown an antiproliferative activity toward tumor cells often definitely better than cisplatin, whereas they have resulted practically inactive against the non-cancer MRC-5 cell line. The mechanism of action of bis-NHC derivative la, particularly active against ovarian cancer cell lines was studied in depth. Through a longitudinally analysis, it is shown that compound la induces apoptosis via DNA damage and release of cytochrome C. We propose compound la as a powerful and specific drug for the therapy of a deadly disease such as high grade serous ovarian cancer. (C) 2019 Elsevier Masson SAS. All rights reserved.
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Univ Ferrara, Dipartimento Sci Vita & Biotecnol, Via Fossato Mortara 74, I-44121 Ferrara, ItalyUniv Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci,Via Torino 155, I-30174 Venice, Italy
Gambari, Roberto
Visentin, Fabiano
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Univ Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci,Via Torino 155, I-30174 Venice, ItalyUniv Ca Foscari, Dipartimento Sci Mol & Nanosistemi, Campus Sci,Via Torino 155, I-30174 Venice, Italy