Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer.
Angela MaselliStefania ParlatoRossella PuglisiCarla RaggiMassimo SpadaDaniele MacchiaGiada PontecorviElisabetta IessiMaria Teresa PaganoFrancesca CirulliLucia GabrieleAlessandra CarèPatrizia ViciLaura PizzutiMaddalena BarbaPaola MatarreseMarina PierdominiciElena OrtonaPublished in: Cells (2019)
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.
Keyphrases
- estrogen receptor
- breast cancer cells
- positive breast cancer
- cell cycle
- endoplasmic reticulum
- cell proliferation
- systemic lupus erythematosus
- type diabetes
- stem cells
- oxidative stress
- signaling pathway
- high resolution
- mesenchymal stem cells
- fatty acid
- cell death
- quantum dots
- insulin resistance
- smoking cessation
- high speed