Sodium orthovanadate associated with pharmacological doses of ascorbate causes an increased generation of ROS in tumor cells that inhibits proliferation and triggers apoptosis

Günther, Tânia Mara Fischer;Kviecinski, Maicon Roberto;Baron, Carla Cristine;Felipe, Karina Bettega;Pedrosa, Rozangela Curi;et.al.
(2013) Biochemical and Biophysical Research Communications — Vol. 430, n° 3, p. 883-888 (2013)

Files

fisher-kviecinski-baron-sodium-biochembiophysicalres.pdf
  • Restricted Access
  • Adobe PDF
  • 1.08 MB
Request a copy

Details

Authors
  • Günther, Tânia Mara Fischer
    Author
  • Kviecinski, Maicon Roberto
    Author
  • Baron, Carla Cristine
    Author
  • Felipe, Karina Bettega
    Author
  • Verrax, JulienUCLouvain
    Author
  • Buc Calderon, PedroUCLouvain
    Author
  • Pedrosa, Rozangela Curi
    Author
Show more
Abstract
Pharmacological doses of ascorbate were evaluated for its ability to potentiate the toxicity of sodium orthovanadate (Na(3)VO(4)) in tumor cells. Cytotoxicity, inhibition of cell proliferation, generation of ROS and DNA fragmentation were assessed in T24 cells. Na(3)VO(4) was cytotoxic against T24 cells (EC(50)=5.8 μM at 24 h), but in the presence of ascorbate (100 μM) the EC(50) fell to 3.3 μM. Na(3)VO(4) plus ascorbate caused a strong inhibition of cell proliferation (up to 20%) and increased the generation of ROS (4-fold). Na(3)VO(4) did not directly cleave plasmid DNA, at this aspect no synergism was found occurring between Na(3)VO(4) and ascorbate once the resulting action of the combination was no greater than that of both substances administered separately. Cells from Ehrlich ascites carcinoma-bearing mice were used to determine the activity of antioxidant enzymes, the extent of the oxidative damage and the type of cell death. Na(3)VO(4) alone, or combined with ascorbate, increased catalase activity, but only Na(3)VO(4) plus ascorbate increased superoxide dismutase activity (up to 4-fold). Oxidative damage on proteins and lipids was higher due to the treatment done with Na(3)VO(4) plus ascorbate (2-3-fold). Ascorbate potentiated apoptosis in tumor cells from mice treated with Na(3)VO(4). The results indicate that pharmacological doses of ascorbate enhance the generation of ROS induced by Na(3)VO(4) in tumor cells causing inhibition of proliferation and apoptosis. Apoptosis induced by orthovanadate and ascorbate is closer related to inhibition on Bcl-xL and activation of Bax. Our data apparently rule out a mechanism of cell demise p53-dependent or related to Cdk2 impairment.
Affiliations

Citations

  • APA
  • Chicago
  • FWB

Günther, T. M. F., Kviecinski, M. R., Baron, C. C., Felipe, K. B., Farias, M. S., da Silva, F. O., Bücker, N. C. F., Pich, C. T., Ferreira, E. A., Wilhelm Filho, D., Verrax, J., Buc Calderon, P., & Pedrosa, R. C. (2013). Sodium orthovanadate associated with pharmacological doses of ascorbate causes an increased generation of ROS in tumor cells that inhibits proliferation and triggers apoptosis. Biochemical and Biophysical Research Communications, 430(3), 883-888. https://doi.org/10.1016/j.bbrc.2012.12.061 (Original work published 2013)