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

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-as...

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Autores principales: Maselli, Angela, Parlato, Stefania, Puglisi, Rossella, Raggi, Carla, Spada, Massimo, Macchia, Daniele, Pontecorvi, Giada, Iessi, Elisabetta, Pagano, Maria Teresa, Cirulli, Francesca, Gabriele, Lucia, Carè, Alessandra, Vici, Patrizia, Pizzuti, Laura, Barba, Maddalena, Matarrese, Paola, Pierdominici, Marina, Ortona, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678306/
https://www.ncbi.nlm.nih.gov/pubmed/31331091
http://dx.doi.org/10.3390/cells8070750
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author Maselli, Angela
Parlato, Stefania
Puglisi, Rossella
Raggi, Carla
Spada, Massimo
Macchia, Daniele
Pontecorvi, Giada
Iessi, Elisabetta
Pagano, Maria Teresa
Cirulli, Francesca
Gabriele, Lucia
Carè, Alessandra
Vici, Patrizia
Pizzuti, Laura
Barba, Maddalena
Matarrese, Paola
Pierdominici, Marina
Ortona, Elena
author_facet Maselli, Angela
Parlato, Stefania
Puglisi, Rossella
Raggi, Carla
Spada, Massimo
Macchia, Daniele
Pontecorvi, Giada
Iessi, Elisabetta
Pagano, Maria Teresa
Cirulli, Francesca
Gabriele, Lucia
Carè, Alessandra
Vici, Patrizia
Pizzuti, Laura
Barba, Maddalena
Matarrese, Paola
Pierdominici, Marina
Ortona, Elena
author_sort Maselli, Angela
collection PubMed
description 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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spelling pubmed-66783062019-08-19 Autoantibodies Specific to ERα 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 Pagano, Maria Teresa Cirulli, Francesca Gabriele, Lucia Carè, Alessandra Vici, Patrizia Pizzuti, Laura Barba, Maddalena Matarrese, Paola Pierdominici, Marina Ortona, Elena Cells Brief Report 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. MDPI 2019-07-19 /pmc/articles/PMC6678306/ /pubmed/31331091 http://dx.doi.org/10.3390/cells8070750 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Maselli, Angela
Parlato, Stefania
Puglisi, Rossella
Raggi, Carla
Spada, Massimo
Macchia, Daniele
Pontecorvi, Giada
Iessi, Elisabetta
Pagano, Maria Teresa
Cirulli, Francesca
Gabriele, Lucia
Carè, Alessandra
Vici, Patrizia
Pizzuti, Laura
Barba, Maddalena
Matarrese, Paola
Pierdominici, Marina
Ortona, Elena
Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer
title Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer
title_full Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer
title_fullStr Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer
title_full_unstemmed Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer
title_short Autoantibodies Specific to ERα are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer
title_sort autoantibodies specific to erα are involved in tamoxifen resistance in hormone receptor positive breast cancer
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678306/
https://www.ncbi.nlm.nih.gov/pubmed/31331091
http://dx.doi.org/10.3390/cells8070750
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