Cells (Jul 2019)

Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer

  • Angela Maselli,
  • Stefania Parlato,
  • Rossella Puglisi,
  • Carla Raggi,
  • Massimo Spada,
  • Daniele Macchia,
  • Giada Pontecorvi,
  • Elisabetta Iessi,
  • Maria Teresa Pagano,
  • Francesca Cirulli,
  • Lucia Gabriele,
  • Alessandra Carè,
  • Patrizia Vici,
  • Laura Pizzuti,
  • Maddalena Barba,
  • Paola Matarrese,
  • Marina Pierdominici,
  • Elena Ortona

DOI
https://doi.org/10.3390/cells8070750
Journal volume & issue
Vol. 8, no. 7
p. 750

Abstract

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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.

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