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      Overexpression of HER2 modulates bcl-2, bcl-XL, and tamoxifen-induced apoptosis in human MCF-7 breast cancer cells.

      Clinical cancer research : an official journal of the American Association for Cancer Research
      Apoptosis, drug effects, Breast Neoplasms, chemistry, drug therapy, pathology, Estrogen Antagonists, pharmacology, Female, Humans, Proto-Oncogene Proteins, analysis, Proto-Oncogene Proteins c-bcl-2, Receptor, ErbB-2, physiology, Receptors, Estrogen, Tamoxifen, Tumor Cells, Cultured, bcl-2-Associated X Protein, bcl-X Protein

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          Abstract

          Overexpression of HER2 in estrogen receptor (ER)-positive human breast tumors has been associated with resistance to endocrine therapy. Here we investigated the effects of HER2 on expression of apoptotic pathways and modulation of tamoxifen-induced apoptosis in ER-positive MCF-7 breast cancer cells. We report that HER2 overexpression in MCF-7 cells is accompanied by up-regulation of antiapoptotic Bcl-2 and Bcl-XL proteins and suppression of tamoxifen-induced apoptosis. In addition, human tumor cell lines that are both ER positive and overexpress HER2 also express enhanced levels of Bcl-2 compared to cells that are either ER positive or overexpress HER2 alone. Our findings suggest that possible deregulation of antiapoptotic Bcl-2 and Bcl-XL may be associated with the enhanced survival of HER2-overexpressing and ER-positive breast cancer cells treated with antiestrogens.

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