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Molecular targeted therapies for breast cancer treatment
Targeting the oestrogen receptor, HER2 (human epidermal growth factor receptor 2) and vascular endothelial growth factor has markedly improved breast cancer therapy. New targeted therapeutic approaches to induction of apoptosis or inhibition of anti-apoptosis, cell cycle progression, signal transduc...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2575526/ https://www.ncbi.nlm.nih.gov/pubmed/18671839 http://dx.doi.org/10.1186/bcr2112 |
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author | Schlotter, Claus M Vogt, Ulf Allgayer, Heike Brandt, Burkhard |
author_facet | Schlotter, Claus M Vogt, Ulf Allgayer, Heike Brandt, Burkhard |
author_sort | Schlotter, Claus M |
collection | PubMed |
description | Targeting the oestrogen receptor, HER2 (human epidermal growth factor receptor 2) and vascular endothelial growth factor has markedly improved breast cancer therapy. New targeted therapeutic approaches to induction of apoptosis or inhibition of anti-apoptosis, cell cycle progression, signal transduction and angiogenesis are described. The molecular pathways and their inhibitory or repair mechanisms are discussed in the preclinical and clinical settings. |
format | Text |
id | pubmed-2575526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25755262008-10-30 Molecular targeted therapies for breast cancer treatment Schlotter, Claus M Vogt, Ulf Allgayer, Heike Brandt, Burkhard Breast Cancer Res Review Targeting the oestrogen receptor, HER2 (human epidermal growth factor receptor 2) and vascular endothelial growth factor has markedly improved breast cancer therapy. New targeted therapeutic approaches to induction of apoptosis or inhibition of anti-apoptosis, cell cycle progression, signal transduction and angiogenesis are described. The molecular pathways and their inhibitory or repair mechanisms are discussed in the preclinical and clinical settings. BioMed Central 2008 2008-07-24 /pmc/articles/PMC2575526/ /pubmed/18671839 http://dx.doi.org/10.1186/bcr2112 Text en Copyright © 2008 BioMed Central Ltd |
spellingShingle | Review Schlotter, Claus M Vogt, Ulf Allgayer, Heike Brandt, Burkhard Molecular targeted therapies for breast cancer treatment |
title | Molecular targeted therapies for breast cancer treatment |
title_full | Molecular targeted therapies for breast cancer treatment |
title_fullStr | Molecular targeted therapies for breast cancer treatment |
title_full_unstemmed | Molecular targeted therapies for breast cancer treatment |
title_short | Molecular targeted therapies for breast cancer treatment |
title_sort | molecular targeted therapies for breast cancer treatment |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2575526/ https://www.ncbi.nlm.nih.gov/pubmed/18671839 http://dx.doi.org/10.1186/bcr2112 |
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