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Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches

Endocrine therapy is the main treatment for hormone receptor-positive (HR+) breast cancer. However, advanced tumors develop resistance to endocrine therapy, rendering it ineffective as the disease progresses. There are several molecular mechanisms of primary and secondary endocrine resistance. Resis...

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Autores principales: Raheem, Farah, Karikalan, Suganya Arunachalam, Batalini, Felipe, El Masry, Aya, Mina, Lida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671474/
https://www.ncbi.nlm.nih.gov/pubmed/38003387
http://dx.doi.org/10.3390/ijms242216198
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author Raheem, Farah
Karikalan, Suganya Arunachalam
Batalini, Felipe
El Masry, Aya
Mina, Lida
author_facet Raheem, Farah
Karikalan, Suganya Arunachalam
Batalini, Felipe
El Masry, Aya
Mina, Lida
author_sort Raheem, Farah
collection PubMed
description Endocrine therapy is the main treatment for hormone receptor-positive (HR+) breast cancer. However, advanced tumors develop resistance to endocrine therapy, rendering it ineffective as the disease progresses. There are several molecular mechanisms of primary and secondary endocrine resistance. Resistance can develop due to either alteration of the estrogen receptor pathway (e.g., ESR1 mutations) or upstream growth factors signaling pathways (e.g., PI3K/Akt/mTOR pathway). Despite progress in the development of molecularly targeted anticancer therapies, the emergence of resistance remains a major limitation and an area of unmet need. In this article, we review the mechanisms of acquired endocrine resistance in HR+ advanced breast cancer and discuss current and future investigational therapeutic approaches.
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spelling pubmed-106714742023-11-11 Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches Raheem, Farah Karikalan, Suganya Arunachalam Batalini, Felipe El Masry, Aya Mina, Lida Int J Mol Sci Review Endocrine therapy is the main treatment for hormone receptor-positive (HR+) breast cancer. However, advanced tumors develop resistance to endocrine therapy, rendering it ineffective as the disease progresses. There are several molecular mechanisms of primary and secondary endocrine resistance. Resistance can develop due to either alteration of the estrogen receptor pathway (e.g., ESR1 mutations) or upstream growth factors signaling pathways (e.g., PI3K/Akt/mTOR pathway). Despite progress in the development of molecularly targeted anticancer therapies, the emergence of resistance remains a major limitation and an area of unmet need. In this article, we review the mechanisms of acquired endocrine resistance in HR+ advanced breast cancer and discuss current and future investigational therapeutic approaches. MDPI 2023-11-11 /pmc/articles/PMC10671474/ /pubmed/38003387 http://dx.doi.org/10.3390/ijms242216198 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Raheem, Farah
Karikalan, Suganya Arunachalam
Batalini, Felipe
El Masry, Aya
Mina, Lida
Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches
title Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches
title_full Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches
title_fullStr Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches
title_full_unstemmed Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches
title_short Metastatic ER+ Breast Cancer: Mechanisms of Resistance and Future Therapeutic Approaches
title_sort metastatic er+ breast cancer: mechanisms of resistance and future therapeutic approaches
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671474/
https://www.ncbi.nlm.nih.gov/pubmed/38003387
http://dx.doi.org/10.3390/ijms242216198
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