Antiestrogens are currently used for treating breast cancer patients who have estrogen receptor-positive tumors. However, patients with advanced disease will eventually develop resistance to the drugs. Therefore, compounds effective on antiestrogen-resistant tumors will be of great importance for future breast cancer treatment. In this study, we have investigated the effect of the chemotherapeutic compound cisplatin using a panel of antiestrogen-resistant breast cancer cell lines established from the human breast cancer cell line MCF-7. We show that the antiestrogen-resistant cells are significantly more sensitive to cisplatin-induced cell death than antiestrogen-sensitive MCF-7 cells and we show that cisplatin induces cell death by activating both the caspase and lysosomal death pathways. The antiestrogen-resistant cell lines express lower levels of antiapoptotic Bcl-2 protein compared with parental MCF-7 cells. Our data show that Bcl-2 can protect antiestrogen-resistant breast cancer cells from cisplatin-induced cell death, indicating that the reduced expression of Bcl-2 in the antiestrogen-resistant cells plays a role in sensitizing the cells to cisplatin treatment. Copyright © 2007 American Association for Cancer Research.
CITATION STYLE
Yde, C. W., Gyrd-Hansen, M., Lykkesfeldt, A. E., Issinger, O. G., & Stenvang, J. (2007). Breast cancer cells with acquired antiestrogen resistance are sensitized to cisplatin-induced cell death. Molecular Cancer Therapeutics, 6(6), 1869–1876. https://doi.org/10.1158/1535-7163.MCT-07-0072
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