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Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4

Endocrine resistance is a major limitation to the successful treatment of estrogen receptor-positive (ER(+)) breast cancer, and the EGFR (epidermal growth factor receptor) and ErbB-2 receptor tyrosine kinases are involved in this process. A recent study now implicates the other two ErbB family membe...

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Detalles Bibliográficos
Autor principal: Sutherland, Robert L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218934/
https://www.ncbi.nlm.nih.gov/pubmed/21639949
http://dx.doi.org/10.1186/bcr2878
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author Sutherland, Robert L
author_facet Sutherland, Robert L
author_sort Sutherland, Robert L
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description Endocrine resistance is a major limitation to the successful treatment of estrogen receptor-positive (ER(+)) breast cancer, and the EGFR (epidermal growth factor receptor) and ErbB-2 receptor tyrosine kinases are involved in this process. A recent study now implicates the other two ErbB family members, ErbB-3 and -4. Exposure of ER(+ )breast cancer cells to the pure antiestrogen, fulvestrant, increased levels of ErbB-3 or ErbB-4 and sensitivity to the growth-stimulatory effects of heregulin ݱ, a potent ligand for these receptors. Thus, the initial growth-inhibitory effects of fulvestrant appear compromised by cellular plasticity that allows rapid compensatory growth stimulation via ErbB-3/4. Further evaluation of pan-ErbB receptor inhibitors in endocrine-resistant disease appears warranted.
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spelling pubmed-32189342011-11-20 Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4 Sutherland, Robert L Breast Cancer Res Editorial Endocrine resistance is a major limitation to the successful treatment of estrogen receptor-positive (ER(+)) breast cancer, and the EGFR (epidermal growth factor receptor) and ErbB-2 receptor tyrosine kinases are involved in this process. A recent study now implicates the other two ErbB family members, ErbB-3 and -4. Exposure of ER(+ )breast cancer cells to the pure antiestrogen, fulvestrant, increased levels of ErbB-3 or ErbB-4 and sensitivity to the growth-stimulatory effects of heregulin ݱ, a potent ligand for these receptors. Thus, the initial growth-inhibitory effects of fulvestrant appear compromised by cellular plasticity that allows rapid compensatory growth stimulation via ErbB-3/4. Further evaluation of pan-ErbB receptor inhibitors in endocrine-resistant disease appears warranted. BioMed Central 2011 2011-05-20 /pmc/articles/PMC3218934/ /pubmed/21639949 http://dx.doi.org/10.1186/bcr2878 Text en Copyright ©2011 BioMed Central Ltd
spellingShingle Editorial
Sutherland, Robert L
Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4
title Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4
title_full Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4
title_fullStr Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4
title_full_unstemmed Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4
title_short Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4
title_sort endocrine resistance in breast cancer: new roles for erbb3 and erbb4
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218934/
https://www.ncbi.nlm.nih.gov/pubmed/21639949
http://dx.doi.org/10.1186/bcr2878
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