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Epidermal growth factor signalling and bone metastasis

Epidermal growth factor (EGF) signalling is well known for its multifaceted functions in development and tissue homoeostasis. The EGF family of ligands and receptors (ERBB family) have also been extensively investigated for their roles in promoting tumourigenesis and metastasis in a variety of cance...

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Detalles Bibliográficos
Autores principales: Lu, X, Kang, Y
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822931/
https://www.ncbi.nlm.nih.gov/pubmed/20010942
http://dx.doi.org/10.1038/sj.bjc.6605490
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author Lu, X
Kang, Y
author_facet Lu, X
Kang, Y
author_sort Lu, X
collection PubMed
description Epidermal growth factor (EGF) signalling is well known for its multifaceted functions in development and tissue homoeostasis. The EGF family of ligands and receptors (ERBB family) have also been extensively investigated for their roles in promoting tumourigenesis and metastasis in a variety of cancer types. Recent findings indicate that EGF signalling is an important mediator of bone metastasis in breast, prostate and kidney cancers. The EGF signalling stimulates the growth of bone metastasis directly by increasing tumour cell proliferation and indirectly by engaging bone stromal cell in metastasis-promoting activities. Therefore, molecular targeting of ERBB receptors may benefit patients with bone metastasis and should be evaluated in clinical trials.
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spelling pubmed-28229312011-02-02 Epidermal growth factor signalling and bone metastasis Lu, X Kang, Y Br J Cancer Minireview Epidermal growth factor (EGF) signalling is well known for its multifaceted functions in development and tissue homoeostasis. The EGF family of ligands and receptors (ERBB family) have also been extensively investigated for their roles in promoting tumourigenesis and metastasis in a variety of cancer types. Recent findings indicate that EGF signalling is an important mediator of bone metastasis in breast, prostate and kidney cancers. The EGF signalling stimulates the growth of bone metastasis directly by increasing tumour cell proliferation and indirectly by engaging bone stromal cell in metastasis-promoting activities. Therefore, molecular targeting of ERBB receptors may benefit patients with bone metastasis and should be evaluated in clinical trials. Nature Publishing Group 2010-02-02 2009-12-15 /pmc/articles/PMC2822931/ /pubmed/20010942 http://dx.doi.org/10.1038/sj.bjc.6605490 Text en Copyright © 2010 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Minireview
Lu, X
Kang, Y
Epidermal growth factor signalling and bone metastasis
title Epidermal growth factor signalling and bone metastasis
title_full Epidermal growth factor signalling and bone metastasis
title_fullStr Epidermal growth factor signalling and bone metastasis
title_full_unstemmed Epidermal growth factor signalling and bone metastasis
title_short Epidermal growth factor signalling and bone metastasis
title_sort epidermal growth factor signalling and bone metastasis
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822931/
https://www.ncbi.nlm.nih.gov/pubmed/20010942
http://dx.doi.org/10.1038/sj.bjc.6605490
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