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Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma
A large number of patients suffering from oesophageal adenocarcinomas do not respond to conventional chemotherapy; therefore, it is necessary to identify new predictive biomarkers and patient signatures to improve patient outcomes and therapy selections. We analysed 87 formalin-fixed and paraffin-em...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179464/ https://www.ncbi.nlm.nih.gov/pubmed/21966358 http://dx.doi.org/10.1371/journal.pone.0023985 |
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author | Berg, Daniela Wolff, Claudia Langer, Rupert Schuster, Tibor Feith, Marcus Slotta-Huspenina, Julia Malinowsky, Katharina Becker, Karl-Friedrich |
author_facet | Berg, Daniela Wolff, Claudia Langer, Rupert Schuster, Tibor Feith, Marcus Slotta-Huspenina, Julia Malinowsky, Katharina Becker, Karl-Friedrich |
author_sort | Berg, Daniela |
collection | PubMed |
description | A large number of patients suffering from oesophageal adenocarcinomas do not respond to conventional chemotherapy; therefore, it is necessary to identify new predictive biomarkers and patient signatures to improve patient outcomes and therapy selections. We analysed 87 formalin-fixed and paraffin-embedded (FFPE) oesophageal adenocarcinoma tissue samples with a reverse phase protein array (RPPA) to examine the expression of 17 cancer-related signalling molecules. Protein expression levels were analysed by unsupervised hierarchical clustering and correlated with clinicopathological parameters and overall patient survival. Proteomic analyses revealed a new, very promising molecular subtype of oesophageal adenocarcinoma patients characterised by low levels of the HSP27 family proteins and high expression of those of the HER family with positive lymph nodes, distant metastases and short overall survival. After confirmation in other independent studies, our results could be the foundation for the development of a Her2-targeted treatment option for this new patient subgroup of oesophageal adenocarcinoma. |
format | Online Article Text |
id | pubmed-3179464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31794642011-09-30 Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma Berg, Daniela Wolff, Claudia Langer, Rupert Schuster, Tibor Feith, Marcus Slotta-Huspenina, Julia Malinowsky, Katharina Becker, Karl-Friedrich PLoS One Research Article A large number of patients suffering from oesophageal adenocarcinomas do not respond to conventional chemotherapy; therefore, it is necessary to identify new predictive biomarkers and patient signatures to improve patient outcomes and therapy selections. We analysed 87 formalin-fixed and paraffin-embedded (FFPE) oesophageal adenocarcinoma tissue samples with a reverse phase protein array (RPPA) to examine the expression of 17 cancer-related signalling molecules. Protein expression levels were analysed by unsupervised hierarchical clustering and correlated with clinicopathological parameters and overall patient survival. Proteomic analyses revealed a new, very promising molecular subtype of oesophageal adenocarcinoma patients characterised by low levels of the HSP27 family proteins and high expression of those of the HER family with positive lymph nodes, distant metastases and short overall survival. After confirmation in other independent studies, our results could be the foundation for the development of a Her2-targeted treatment option for this new patient subgroup of oesophageal adenocarcinoma. Public Library of Science 2011-09-23 /pmc/articles/PMC3179464/ /pubmed/21966358 http://dx.doi.org/10.1371/journal.pone.0023985 Text en Berg 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Berg, Daniela Wolff, Claudia Langer, Rupert Schuster, Tibor Feith, Marcus Slotta-Huspenina, Julia Malinowsky, Katharina Becker, Karl-Friedrich Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma |
title | Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma |
title_full | Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma |
title_fullStr | Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma |
title_full_unstemmed | Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma |
title_short | Discovery of New Molecular Subtypes in Oesophageal Adenocarcinoma |
title_sort | discovery of new molecular subtypes in oesophageal adenocarcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179464/ https://www.ncbi.nlm.nih.gov/pubmed/21966358 http://dx.doi.org/10.1371/journal.pone.0023985 |
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