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Cisplatin and its dibromido analogue: a comparison of chemical and biological profiles.
Marzo, Tiziano; Bartoli, Gianluca; Gabbiani, Chiara; Pescitelli, Gennaro; Severi, Mirko; Pillozzi, Serena; Michelucci, Elena; Fiorini, Benedetta; Arcangeli, Annarosa; Quiroga, Adóracion G; Messori, Luigi.
Afiliação
  • Marzo T; Laboratory of Metals in Medicine (MetMed), Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019, Sesto Fiorentino, Italy. tiziano.marzo@unifi.it.
  • Bartoli G; Department of Chemistry and Industrial Chemistry, University of Pisa, via Moruzzi, 3, 56124, Pisa, Italy. tiziano.marzo@unifi.it.
  • Gabbiani C; Department of Experimental and Clinical Medicine, University of Florence, Viale GB Morgagni 50, 50134, Florence, Italy.
  • Pescitelli G; Department of Chemistry and Industrial Chemistry, University of Pisa, via Moruzzi, 3, 56124, Pisa, Italy.
  • Severi M; Department of Chemistry and Industrial Chemistry, University of Pisa, via Moruzzi, 3, 56124, Pisa, Italy.
  • Pillozzi S; Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019, Sesto Fiorentino, Italy.
  • Michelucci E; Department of Experimental and Clinical Medicine, University of Florence, Viale GB Morgagni 50, 50134, Florence, Italy.
  • Fiorini B; Mass Spectrometry Centre (CISM), University of Florence, Via U. Schiff 6, 50019, Sesto Fiorentino, Italy.
  • Arcangeli A; Laboratory of Metals in Medicine (MetMed), Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019, Sesto Fiorentino, Italy.
  • Quiroga AG; Department of Experimental and Clinical Medicine, University of Florence, Viale GB Morgagni 50, 50134, Florence, Italy.
  • Messori L; Department of Inorganic Chemistry, Universidad Autonóma de Madrid, C/Francisco Tomás y Valiente 7, 28049, Madrid, Spain.
Biometals ; 29(3): 535-42, 2016 06.
Article em En | MEDLINE | ID: mdl-27086032
The dibromido analogue of cisplatin, cis-PtBr2(NH3)2 (cisPtBr2 hereafter), has been prepared and characterised. Its solution behaviour in standard phosphate buffer, at pH 7.4, was investigated spectrophotometrically and found to reproduce quite closely that of cisplatin; indeed, progressive sequential release of the two halide ligands typically occurs as in the case of cisplatin, with a roughly similar kinetics. Afterward, patterns of reactivity toward model proteins and standard ctDNA were explored and the nature of the resulting interactions elucidated. The antiproliferative properties were then evaluated in four representative cancer cell lines, namely A549 (human lung cancer), HCT116 (human colon cancer), IGROV-1 (human ovarian cancer) and FLG 29.1 (human acute myeloid leukaemia). Cytotoxic properties in line with those of cisplatin were highlighted. From these studies an overall chemical and biological profile emerges for cisPtBr2 closely matching that of cisplatin; the few slight, but meaningful differences that were underscored might be advantageously exploited for clinical application.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Brometos / Cisplatino / Antineoplásicos Limite: Humans Idioma: En Revista: Biometals Assunto da revista: BIOQUIMICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Brometos / Cisplatino / Antineoplásicos Limite: Humans Idioma: En Revista: Biometals Assunto da revista: BIOQUIMICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Itália