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HER2 expression as a potential marker for response to therapy targeted to the EGFR
Since human epidermal growth factor receptor 2 (HER2) is known to participate with the epidermal growth factor receptor (EGFR) in mitogenic signalling, we hypothesised that HER2 overexpression might indicate responsiveness to EGFR targeted therapies. MCF7 breast cancer cells transfected with the HER...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361260/ https://www.ncbi.nlm.nih.gov/pubmed/16622439 http://dx.doi.org/10.1038/sj.bjc.6603078 |
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author | Emlet, D R Schwartz, R Brown, K A Pollice, A A Smith, C A Shackney, S E |
author_facet | Emlet, D R Schwartz, R Brown, K A Pollice, A A Smith, C A Shackney, S E |
author_sort | Emlet, D R |
collection | PubMed |
description | Since human epidermal growth factor receptor 2 (HER2) is known to participate with the epidermal growth factor receptor (EGFR) in mitogenic signalling, we hypothesised that HER2 overexpression might indicate responsiveness to EGFR targeted therapies. MCF7 breast cancer cells transfected with the HER2 gene were subcloned to establish a set of genetically related cell lines expressing graded levels of HER2 by immunoblot analysis. The subcloned cell lines and parental MCF7 cells were characterised by their growth characteristics, and cell by cell patterns of EGFR, HER2 and HER3 expression as well as levels of phosphorylated mitogen-activated protein kinase (MAPK) and AKT by laser scanning cytometry (LSC). Growth inhibition assays were used to characterise response to EGFR targeted therapy, and to determine the relationship between therapeutic response and levels of tyrosine kinase expression. The levels of growth inhibition of AG1478 and of the AG1478-trastuzumab combinations were correlated with levels of HER2 expression among the different cell lines. Among EGFR, HER2 and HER3, HER2 overexpression was the best single predictive marker, but combinations of two markers provided additional predictive information. |
format | Text |
id | pubmed-2361260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23612602009-09-10 HER2 expression as a potential marker for response to therapy targeted to the EGFR Emlet, D R Schwartz, R Brown, K A Pollice, A A Smith, C A Shackney, S E Br J Cancer Translational Therapeutics Since human epidermal growth factor receptor 2 (HER2) is known to participate with the epidermal growth factor receptor (EGFR) in mitogenic signalling, we hypothesised that HER2 overexpression might indicate responsiveness to EGFR targeted therapies. MCF7 breast cancer cells transfected with the HER2 gene were subcloned to establish a set of genetically related cell lines expressing graded levels of HER2 by immunoblot analysis. The subcloned cell lines and parental MCF7 cells were characterised by their growth characteristics, and cell by cell patterns of EGFR, HER2 and HER3 expression as well as levels of phosphorylated mitogen-activated protein kinase (MAPK) and AKT by laser scanning cytometry (LSC). Growth inhibition assays were used to characterise response to EGFR targeted therapy, and to determine the relationship between therapeutic response and levels of tyrosine kinase expression. The levels of growth inhibition of AG1478 and of the AG1478-trastuzumab combinations were correlated with levels of HER2 expression among the different cell lines. Among EGFR, HER2 and HER3, HER2 overexpression was the best single predictive marker, but combinations of two markers provided additional predictive information. Nature Publishing Group 2006-04-24 2006-04-04 /pmc/articles/PMC2361260/ /pubmed/16622439 http://dx.doi.org/10.1038/sj.bjc.6603078 Text en Copyright © 2006 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 | Translational Therapeutics Emlet, D R Schwartz, R Brown, K A Pollice, A A Smith, C A Shackney, S E HER2 expression as a potential marker for response to therapy targeted to the EGFR |
title | HER2 expression as a potential marker for response to therapy targeted to the EGFR |
title_full | HER2 expression as a potential marker for response to therapy targeted to the EGFR |
title_fullStr | HER2 expression as a potential marker for response to therapy targeted to the EGFR |
title_full_unstemmed | HER2 expression as a potential marker for response to therapy targeted to the EGFR |
title_short | HER2 expression as a potential marker for response to therapy targeted to the EGFR |
title_sort | her2 expression as a potential marker for response to therapy targeted to the egfr |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361260/ https://www.ncbi.nlm.nih.gov/pubmed/16622439 http://dx.doi.org/10.1038/sj.bjc.6603078 |
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