1. Academic Validation
  2. Antioxidant, anticancer activities and mechanistic studies of the flavone glycoside diosmin and its oxidovanadium(IV) complex. Interactions with bovine serum albumin

Antioxidant, anticancer activities and mechanistic studies of the flavone glycoside diosmin and its oxidovanadium(IV) complex. Interactions with bovine serum albumin

  • Bioorg Med Chem. 2016 Sep 15;24(18):4108-4119. doi: 10.1016/j.bmc.2016.06.053.
Luciana Naso 1 Valeria R Martínez 1 Luis Lezama 2 Clarisa Salado 3 María Valcarcel 3 Evelina G Ferrer 1 Patricia A M Williams 4
Affiliations

Affiliations

  • 1 Centro de Química Inorgánica (CEQUINOR, CONICET, UNLP), Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Bv. 120 N° 1465 (62 y 63), 1900 La Plata, Argentina.
  • 2 Departamento de Química Inorgánica, Facultad de Ciencia y Tecnología, Universidad del País Vasco UPV/EHU, PO Box 644, 48080 Bilbao, Spain; BCMaterials, Parque científico y Tecnológico de Bizkaia, Edificio 500-1, 48160 Derio, Spain.
  • 3 Innoprot SL, Parque científico y Tecnológico de Bizkaia, Edificio 502-P1, 48160 Derio, Spain.
  • 4 Centro de Química Inorgánica (CEQUINOR, CONICET, UNLP), Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Bv. 120 N° 1465 (62 y 63), 1900 La Plata, Argentina. Electronic address: williams@quimica.unlp.edu.ar.
Abstract

The natural antioxidant flavonoid diosmin, found in citric fruits, showed low antioxidant properties among Other Flavonoids due to its structural characteristics and low cytotoxicity against lung (A549) and breast (T47D, SKBR3 and MDAMB231) Cancer cell lines. The Anticancer behavior has been improved by the metal complex generated with the flavonoid and the oxidovanadium(IV) ion. This new complex, [VO(dios)(OH)3]Na5·6H2O (VOdios), has been synthesized and characterized both in solid and solution states. The interaction of the metal ion through the sugar moiety of diosmin precluded the improvement of the antioxidant effects. However, the cell-killing effects tested in human lung A549 and breast T47D, SKBR3 and MDAMB231 Cancer cell lines, were enhanced by complexation. The anti-proliferative effects on the human lung Cancer cell line were accompanied by cellular ROS generation and an increase in cytoplasm condensation. The breast Cancer cell lines did not produce caspase3/7 activation, mitochondrial potential reduction and ROS generation. Therefore, a non-apoptotic form of cell death in a caspase- and oxidative stress-independent manner has been proposed. The protein binding ability has been monitored by the quenching of tryptophan emission in the presence of the compounds using bovine serum albumin (BSA) as a model protein. Both compounds could be distributed and transported in vivo and the complex displayed stronger binding affinity and higher contributions to the hydrogen bond and van der Waals forces.

Keywords

Anticancer; Antioxidant; BSA binding; Diosmin; Oxidovanadium(IV) complexes.

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