Significance of mitochondrial calcium and nitric oxide for apoptosis of human breast cancer cells induced by tamoxifen and etoposide

  • Authors:
    • Arti Parihar
    • Mordhwaj S. Parihar
    • Pedram Ghafourifar
  • View Affiliations

  • Published online on: March 1, 2008     https://doi.org/10.3892/ijmm.21.3.317
  • Pages: 317-324
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Abstract

In the present study, we tested the significance of mitochondria for apoptosis upon exposure to tamoxifen and etoposide using two human breast cancer cell lines, MCF-7 and MDA-MB-231. We showed that both tamoxifen and etoposide induced apoptosis, increased intramitochondrial calcium and nitric oxide, and decreased mitochondrial transmembrane potential in both cell lines. Both drugs increased mitochondrial protein tyrosine nitration and caused release of cytochrome c from the mitochondria of both cell lines. This study suggests that tamoxifen and etoposide utilize a common mechanism to induce apoptosis in MCF-7 and MDA-MB-231 cells.

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March 2008
Volume 21 Issue 3

Print ISSN: 1107-3756
Online ISSN:1791-244X

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Spandidos Publications style
Parihar A, Parihar MS and Ghafourifar P: Significance of mitochondrial calcium and nitric oxide for apoptosis of human breast cancer cells induced by tamoxifen and etoposide. Int J Mol Med 21: 317-324, 2008
APA
Parihar, A., Parihar, M.S., & Ghafourifar, P. (2008). Significance of mitochondrial calcium and nitric oxide for apoptosis of human breast cancer cells induced by tamoxifen and etoposide. International Journal of Molecular Medicine, 21, 317-324. https://doi.org/10.3892/ijmm.21.3.317
MLA
Parihar, A., Parihar, M. S., Ghafourifar, P."Significance of mitochondrial calcium and nitric oxide for apoptosis of human breast cancer cells induced by tamoxifen and etoposide". International Journal of Molecular Medicine 21.3 (2008): 317-324.
Chicago
Parihar, A., Parihar, M. S., Ghafourifar, P."Significance of mitochondrial calcium and nitric oxide for apoptosis of human breast cancer cells induced by tamoxifen and etoposide". International Journal of Molecular Medicine 21, no. 3 (2008): 317-324. https://doi.org/10.3892/ijmm.21.3.317