JBIC Journal of Biological Inorganic Chemistry

, Volume 20, Issue 7, pp 1175–1191 | Cite as

Oxidovanadium(IV) complexes with chrysin and silibinin: anticancer activity and mechanisms of action in a human colon adenocarcinoma model

  • I. E. León
  • J. F. Cadavid-Vargas
  • I. Tiscornia
  • V. Porro
  • S. Castelli
  • P. Katkar
  • A. Desideri
  • M. Bollati-Fogolin
  • S. B. Etcheverry
Original Paper

Abstract

Vanadium compounds were studied during recent years to be considered as a representative of a new class of nonplatinum metal antitumor agents in combination to its low toxicity. On the other hand, flavonoids are a wide family of polyphenolic compounds synthesized by plants that display many interesting biological effects. Since coordination of ligands to metals can improve the pharmacological properties, we report herein, for the first time, a exhaustive study of the mechanisms of action of two oxidovanadium(IV) complexes with the flavonoids: silibinin Na2[VO(silibinin)2]·6H2O (VOsil) and chrysin [VO(chrysin)2EtOH]2 (VOchrys) on human colon adenocarcinoma derived cell line HT-29. The complexes inhibited the cell viability of colon adenocarcinoma cells in a dose dependent manner with a greater potency than that the free ligands and free metal, demonstrating the benefit of complexation. The decrease of the ratio of the amount of reduced glutathione to the amount of oxidized glutathione were involved in the deleterious effects of both complexes. Besides, VOchrys caused cell cycle arrest in G2/M phase while VOsil activated caspase 3 and triggering the cells directly to apoptosis. Moreover, VOsil diminished the NF-kB activation via increasing the sensitivity of cells to apoptosis. On the other hand, VOsil inhibited the topoisomerase IB activity concluding that this is important target involved in the anticancer vanadium effects. As a whole, the results presented herein demonstrate that VOsil has a stronger deleterious action than VOchrys on HT-29 cells, whereby suggesting that Vosil is the potentially best candidate for future use in alternative anti-tumor treatments.

Graphical Abstract

Keywords

Metal based drug HT-29 human colon adenocarcinoma cells Mechanisms of action Flavonoids Vanadium 

Supplementary material

775_2015_1298_MOESM1_ESM.pdf (190 kb)
Supplementary material 1 (PDF 190 kb)

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Copyright information

© SBIC 2015

Authors and Affiliations

  • I. E. León
    • 1
    • 2
  • J. F. Cadavid-Vargas
    • 1
    • 2
  • I. Tiscornia
    • 3
  • V. Porro
    • 3
  • S. Castelli
    • 4
  • P. Katkar
    • 4
  • A. Desideri
    • 4
  • M. Bollati-Fogolin
    • 3
  • S. B. Etcheverry
    • 1
    • 2
  1. 1.Cátedra de Bioquímica Patológica, Facultad Ciencias ExactasUniversidad Nacional de La PlataLa PlataArgentina
  2. 2.Centro de Química Inorgánica (CEQUINOR-CONICET), Facultad de Ciencias ExactasUniversidad Nacional de La PlataLa PlataArgentina
  3. 3.Unidad de Biología Celular, Institut Pasteur de MontevideoMontevideoUruguay
  4. 4.Department of BiologyUniversity of Rome “Tor Vergata”RomeItaly

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