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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
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.
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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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