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HER2 therapy: Molecular mechanisms of trastuzumab resistance
Trastuzumab is a monoclonal antibody targeted against the HER2 tyrosine kinase receptor. The majority of patients with metastatic breast cancer who initially respond to trastuzumab develop resistance within one year of treatment initiation, and in the adjuvant setting 15% of patients still relapse d...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797036/ https://www.ncbi.nlm.nih.gov/pubmed/17096862 http://dx.doi.org/10.1186/bcr1612 |
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author | Nahta, Rita Esteva, Francisco J |
author_facet | Nahta, Rita Esteva, Francisco J |
author_sort | Nahta, Rita |
collection | PubMed |
description | Trastuzumab is a monoclonal antibody targeted against the HER2 tyrosine kinase receptor. The majority of patients with metastatic breast cancer who initially respond to trastuzumab develop resistance within one year of treatment initiation, and in the adjuvant setting 15% of patients still relapse despite trastuzumab-based therapy. In this review, we discuss potential mechanisms of antitumor activity by trastuzumab, and how these mechanisms become altered to promote therapeutic resistance. We also discuss novel therapies that may improve the efficacy of trastuzumab, and that offer hope that the survival of breast cancer patients with HER2-overexpressing tumors can be vastly improved. |
format | Text |
id | pubmed-1797036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-17970362007-02-13 HER2 therapy: Molecular mechanisms of trastuzumab resistance Nahta, Rita Esteva, Francisco J Breast Cancer Res Review Trastuzumab is a monoclonal antibody targeted against the HER2 tyrosine kinase receptor. The majority of patients with metastatic breast cancer who initially respond to trastuzumab develop resistance within one year of treatment initiation, and in the adjuvant setting 15% of patients still relapse despite trastuzumab-based therapy. In this review, we discuss potential mechanisms of antitumor activity by trastuzumab, and how these mechanisms become altered to promote therapeutic resistance. We also discuss novel therapies that may improve the efficacy of trastuzumab, and that offer hope that the survival of breast cancer patients with HER2-overexpressing tumors can be vastly improved. BioMed Central 2006 2006-11-06 /pmc/articles/PMC1797036/ /pubmed/17096862 http://dx.doi.org/10.1186/bcr1612 Text en Copyright © 2006 BioMed Central Ltd |
spellingShingle | Review Nahta, Rita Esteva, Francisco J HER2 therapy: Molecular mechanisms of trastuzumab resistance |
title | HER2 therapy: Molecular mechanisms of trastuzumab resistance |
title_full | HER2 therapy: Molecular mechanisms of trastuzumab resistance |
title_fullStr | HER2 therapy: Molecular mechanisms of trastuzumab resistance |
title_full_unstemmed | HER2 therapy: Molecular mechanisms of trastuzumab resistance |
title_short | HER2 therapy: Molecular mechanisms of trastuzumab resistance |
title_sort | her2 therapy: molecular mechanisms of trastuzumab resistance |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797036/ https://www.ncbi.nlm.nih.gov/pubmed/17096862 http://dx.doi.org/10.1186/bcr1612 |
work_keys_str_mv | AT nahtarita her2therapymolecularmechanismsoftrastuzumabresistance AT estevafranciscoj her2therapymolecularmechanismsoftrastuzumabresistance |