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.
Autoantibodies specific to ERa are involved in tamoxifen resistance in hormone receptor positive breast cancer / Maselli, Angela; Parlato, Stefania; Puglisi, Rossella; Raggi, Carla; Spada, Massimo; Macchia, Daniele; Pontecorvi, Giada; Iessi, Elisabetta; Teresa Pagano, Maria; Cirulli, Francesca; Gabriele, Lucia; Carè, Alessandra; Vici, Patrizia; Pizzuti, Laura; Barba, Maddalena; Matarrese, Paola; Pierdominici, Marina; Ortona, Elena. - In: CELLS. - ISSN 2073-4409. - 8:7(2019), pp. 1-14. [10.3390/cells8070750]
Autoantibodies specific to ERa are involved in tamoxifen resistance in hormone receptor positive breast cancer
Rossella Puglisi;Giada Pontecorvi;Maria Teresa Pagano;Francesca Cirulli;Laura Pizzuti;Maddalena Barba;
2019
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.File | Dimensione | Formato | |
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