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Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification

Cross-communication between different signalling systems is critical for the integration of multiple and changing environmental influences on individual cells. The epidermal growth factor receptor (EGFR) has been identified as a key element in the complex signalling network that is utilized by vario...

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Detalles Bibliográficos
Autores principales: Prenzel, Norbert, Zwick, Esther, Leserer, Michael, Ullrich, Axel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138773/
https://www.ncbi.nlm.nih.gov/pubmed/11250708
http://dx.doi.org/10.1186/bcr52
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author Prenzel, Norbert
Zwick, Esther
Leserer, Michael
Ullrich, Axel
author_facet Prenzel, Norbert
Zwick, Esther
Leserer, Michael
Ullrich, Axel
author_sort Prenzel, Norbert
collection PubMed
description Cross-communication between different signalling systems is critical for the integration of multiple and changing environmental influences on individual cells. The epidermal growth factor receptor (EGFR) has been identified as a key element in the complex signalling network that is utilized by various classes of cell-surface receptors. This nonclassical mode of signalling system cross-talk, in distinction to receptor activation induced by cognate ligands, has been termed 'signal transactivation'. With the EGFR as the convergence point and distribution focus, this scenario may involve signals emitted by other members of the tyrosine kinase family, cytokine receptors, ion channels, G-protein-coupled receptors and integrins.
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spelling pubmed-1387732003-02-27 Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification Prenzel, Norbert Zwick, Esther Leserer, Michael Ullrich, Axel Breast Cancer Res Review Cross-communication between different signalling systems is critical for the integration of multiple and changing environmental influences on individual cells. The epidermal growth factor receptor (EGFR) has been identified as a key element in the complex signalling network that is utilized by various classes of cell-surface receptors. This nonclassical mode of signalling system cross-talk, in distinction to receptor activation induced by cognate ligands, has been termed 'signal transactivation'. With the EGFR as the convergence point and distribution focus, this scenario may involve signals emitted by other members of the tyrosine kinase family, cytokine receptors, ion channels, G-protein-coupled receptors and integrins. BioMed Central 2000 2000-03-25 /pmc/articles/PMC138773/ /pubmed/11250708 http://dx.doi.org/10.1186/bcr52 Text en Copyright © 2000 Current Science Ltd
spellingShingle Review
Prenzel, Norbert
Zwick, Esther
Leserer, Michael
Ullrich, Axel
Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification
title Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification
title_full Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification
title_fullStr Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification
title_full_unstemmed Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification
title_short Tyrosine kinase signalling in breast cancer: Epidermal growth factor receptor - convergence point for signal integration and diversification
title_sort tyrosine kinase signalling in breast cancer: epidermal growth factor receptor - convergence point for signal integration and diversification
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138773/
https://www.ncbi.nlm.nih.gov/pubmed/11250708
http://dx.doi.org/10.1186/bcr52
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