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The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers
INTRODUCTION: Expression of human epidermal growth factor receptor (HER)2 and HER3 have been investigated in small BTC studies using variable scoring systems. METHODS: HER2 and HER3 overexpression/amplification were explored following internationally agreed guidelines using immunohistochemistry (IHC...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193702/ https://www.ncbi.nlm.nih.gov/pubmed/30335866 http://dx.doi.org/10.1371/journal.pone.0206007 |
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author | Lamarca, Angela Galdy, Salvatore Barriuso, Jorge Moghadam, Sharzad Beckett, Elizabeth Rogan, Jane Backen, Alison Billington, Catherine McNamara, Mairéad G. Hubner, Richard A. Cramer, Angela Valle, Juan W. |
author_facet | Lamarca, Angela Galdy, Salvatore Barriuso, Jorge Moghadam, Sharzad Beckett, Elizabeth Rogan, Jane Backen, Alison Billington, Catherine McNamara, Mairéad G. Hubner, Richard A. Cramer, Angela Valle, Juan W. |
author_sort | Lamarca, Angela |
collection | PubMed |
description | INTRODUCTION: Expression of human epidermal growth factor receptor (HER)2 and HER3 have been investigated in small BTC studies using variable scoring systems. METHODS: HER2 and HER3 overexpression/amplification were explored following internationally agreed guidelines using immunohistochemistry (IHC) and fluorescent in-situ hybridisation (FISH), respectively. Logistic regression and survival analysis (Kaplan Meier, Log rank test and Cox Regression) were used for statistical analysis. RESULTS: Sixty-seven eligible patients with Stage I/II (31.3%) or III/IV (68.7%) disease at diagnosis were included. Membrane HER2 overexpression/amplification was identified in 1 patient (1%). HER3 overexpression was predominantly cytoplasmic; the rate of overexpression/amplification of HER3 in membrane and cytoplasm was 16% [ampullary cancer (AMP) (1/13; 8%), gallbladder cancer (GBC) (1/10; 10%), intra-hepatic cholangiocarcinoma (ICC) (6/26; 23%), extra-hepatic cholangiocarcinoma (ECC) (3/18; 17%)] and 24% [AMP (1/13; 8%), GBC (1/10; 10%), ICC (10/26; 38%), ECC (4/18; 22%)], respectively. CONCLUSIONS: A significant subset of patients with BTC expressed HER3. Inhibition of HER3 warrants further investigation. A better understanding of the downstream effects of HER3 in BTC requires further mechanistic investigations to identify new biomarkers and improve patient selection for future clinical trials. |
format | Online Article Text |
id | pubmed-6193702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61937022018-11-05 The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers Lamarca, Angela Galdy, Salvatore Barriuso, Jorge Moghadam, Sharzad Beckett, Elizabeth Rogan, Jane Backen, Alison Billington, Catherine McNamara, Mairéad G. Hubner, Richard A. Cramer, Angela Valle, Juan W. PLoS One Research Article INTRODUCTION: Expression of human epidermal growth factor receptor (HER)2 and HER3 have been investigated in small BTC studies using variable scoring systems. METHODS: HER2 and HER3 overexpression/amplification were explored following internationally agreed guidelines using immunohistochemistry (IHC) and fluorescent in-situ hybridisation (FISH), respectively. Logistic regression and survival analysis (Kaplan Meier, Log rank test and Cox Regression) were used for statistical analysis. RESULTS: Sixty-seven eligible patients with Stage I/II (31.3%) or III/IV (68.7%) disease at diagnosis were included. Membrane HER2 overexpression/amplification was identified in 1 patient (1%). HER3 overexpression was predominantly cytoplasmic; the rate of overexpression/amplification of HER3 in membrane and cytoplasm was 16% [ampullary cancer (AMP) (1/13; 8%), gallbladder cancer (GBC) (1/10; 10%), intra-hepatic cholangiocarcinoma (ICC) (6/26; 23%), extra-hepatic cholangiocarcinoma (ECC) (3/18; 17%)] and 24% [AMP (1/13; 8%), GBC (1/10; 10%), ICC (10/26; 38%), ECC (4/18; 22%)], respectively. CONCLUSIONS: A significant subset of patients with BTC expressed HER3. Inhibition of HER3 warrants further investigation. A better understanding of the downstream effects of HER3 in BTC requires further mechanistic investigations to identify new biomarkers and improve patient selection for future clinical trials. Public Library of Science 2018-10-18 /pmc/articles/PMC6193702/ /pubmed/30335866 http://dx.doi.org/10.1371/journal.pone.0206007 Text en © 2018 Lamarca et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lamarca, Angela Galdy, Salvatore Barriuso, Jorge Moghadam, Sharzad Beckett, Elizabeth Rogan, Jane Backen, Alison Billington, Catherine McNamara, Mairéad G. Hubner, Richard A. Cramer, Angela Valle, Juan W. The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers |
title | The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers |
title_full | The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers |
title_fullStr | The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers |
title_full_unstemmed | The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers |
title_short | The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers |
title_sort | her3 pathway as a potential target for inhibition in patients with biliary tract cancers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193702/ https://www.ncbi.nlm.nih.gov/pubmed/30335866 http://dx.doi.org/10.1371/journal.pone.0206007 |
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