Abstract
Tamoxifen resistance is a major hurdle in the treatment of estrogen receptor (ER)-positive breast cancer. The mechanisms of tamoxifen resistance are not fully understood although several underlying molecular events have been suggested. Recently, we identified autoantibodies reacting with membrane-associated ERα (anti-ERα Abs) in sera of breast cancer patients, able to promote tumor growth. Here, we investigated whether anti-ERα Abs purified from sera of ER-positive breast cancer patients could contribute to tamoxifen resistance. Anti-ERα Abs inhibited tamoxifen-mediated effects on cell cycle and proliferation in MCF-7 cells. Moreover, anti-ERα Abs hampered the tamoxifen-mediated reduction of tumor growth in SCID mice xenografted with breast tumor. Notably, simvastatin-mediated disaggregation of lipid rafts, where membrane-associated ERα is embedded, restored tamoxifen sensitivity, preventing anti-ERα Abs effects. In conclusion, detection of serum anti-ERα Abs may help predict tamoxifen resistance and concur to appropriately inform therapeutic decisions concerning hormone therapy in ER-positive breast cancer patients.
Original language | English |
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Journal | Cells |
Volume | 8 |
Issue number | 7 |
DOIs | |
Publication status | Published - Jul 19 2019 |
Keywords
- Adult
- Aged
- Aged, 80 and over
- Animals
- Antineoplastic Agents, Hormonal/immunology
- Autoantibodies/blood
- Breast Neoplasms/drug therapy
- Drug Resistance, Neoplasm/immunology
- Estrogen Receptor alpha/immunology
- Female
- Humans
- MCF-7 Cells
- Mice
- Mice, SCID
- Middle Aged
- Tamoxifen/therapeutic use
- Xenograft Model Antitumor Assays