Cargando…
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...
Autor principal: | |
---|---|
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 |
_version_ | 1782216760946065408 |
---|---|
author | Sutherland, Robert L |
author_facet | Sutherland, Robert L |
author_sort | Sutherland, Robert L |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-3218934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sutherlandrobertl endocrineresistanceinbreastcancernewrolesforerbb3anderbb4 |