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J Inorg Biochem ; 129: 127-34, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-24121302

RESUMEN

In this study we report the synthesis, the X-ray crystal structure and the in vivo tumor growth suppression and nephroprotective activity of bis-dimethylsulfoxide-cis-tetrachlorodi-µ-pivalatodirhenium(III), cis-Re2[(CH3)3CCOO]2Cl4·2(CH3)2SO (I). The interactions of I with DNA were also investigated by electrophoretic mobility shift assays, electronic absorption titrations, ΔTm and viscosity measurements, which indicate that compound I interacts relatively strongly with the DNA (Kb 2.2×10(3)M(-1)), most likely by forming covalent interstrand cross-links, and by kinking and unwinding supercoiled DNA; moreover, DNA cleavage by I is enhanced in the presence of redox-active species. The in vivo antitumor activity of I is considerable and is accompanied by significant elimination of red blood cell and kidney damage. Remarkably, compound I in combination with cisplatin (combined Re-Pt antitumor system) led to suppression of tumor growth or complete tumor elimination. The antihemolytic and nephroprotective abilities of I only or as a part of the Re-Pt antitumor system were established and a possible mechanism for the influence of I on these properties, involving erythropoietin production, is proposed.


Asunto(s)
Antineoplásicos , ADN de Neoplasias , Neoplasias Experimentales/tratamiento farmacológico , Renio , Animales , Antineoplásicos/síntesis química , Antineoplásicos/química , Antineoplásicos/farmacología , Cisplatino/química , Cisplatino/farmacología , Cristalografía por Rayos X , ADN de Neoplasias/química , ADN de Neoplasias/metabolismo , Ensayos de Selección de Medicamentos Antitumorales , Neoplasias Experimentales/metabolismo , Neoplasias Experimentales/patología , Oxidación-Reducción , Ratas , Ratas Wistar , Renio/química , Renio/farmacología
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