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Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus

Barrett esophagus (BE) is caused by chronic gastroesophageal reflux and predisposes to the development of esophageal adenocarcinoma through different grades of dysplasia. Only a subset of BE patients will finally develop esophageal adenocarcinoma. The majority will therefore not benefit from an endo...

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Autores principales: Kerkhof, Marjon, Kusters, Johannes G., van Dekken, Herman, Kuipers, Ernst J., Siersema, Peter D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618977/
https://www.ncbi.nlm.nih.gov/pubmed/18032827
http://dx.doi.org/10.1155/2007/814950
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author Kerkhof, Marjon
Kusters, Johannes G.
van Dekken, Herman
Kuipers, Ernst J.
Siersema, Peter D.
author_facet Kerkhof, Marjon
Kusters, Johannes G.
van Dekken, Herman
Kuipers, Ernst J.
Siersema, Peter D.
author_sort Kerkhof, Marjon
collection PubMed
description Barrett esophagus (BE) is caused by chronic gastroesophageal reflux and predisposes to the development of esophageal adenocarcinoma through different grades of dysplasia. Only a subset of BE patients will finally develop esophageal adenocarcinoma. The majority will therefore not benefit from an endoscopic surveillance program, based on the histological identification of dysplasia. Several studies have been performed to find additional biomarkers that can be used to detect the subgroup of patients with an increased risk of developing malignancy in BE. In this review, we will summarize the most promising tissue biomarkers, i.e. proliferation/cell cycle proteins, tumor suppressor genes, adhesion molecules, DNA ploidy status and inflammation associated markers, that can be used for risk stratification in BE, and discuss their respective clinical application.
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spelling pubmed-46189772016-01-12 Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus Kerkhof, Marjon Kusters, Johannes G. van Dekken, Herman Kuipers, Ernst J. Siersema, Peter D. Cell Oncol Other Barrett esophagus (BE) is caused by chronic gastroesophageal reflux and predisposes to the development of esophageal adenocarcinoma through different grades of dysplasia. Only a subset of BE patients will finally develop esophageal adenocarcinoma. The majority will therefore not benefit from an endoscopic surveillance program, based on the histological identification of dysplasia. Several studies have been performed to find additional biomarkers that can be used to detect the subgroup of patients with an increased risk of developing malignancy in BE. In this review, we will summarize the most promising tissue biomarkers, i.e. proliferation/cell cycle proteins, tumor suppressor genes, adhesion molecules, DNA ploidy status and inflammation associated markers, that can be used for risk stratification in BE, and discuss their respective clinical application. IOS Press 2007 2007-11-21 /pmc/articles/PMC4618977/ /pubmed/18032827 http://dx.doi.org/10.1155/2007/814950 Text en Copyright © 2007 Hindawi Publishing Corporation and the authors.
spellingShingle Other
Kerkhof, Marjon
Kusters, Johannes G.
van Dekken, Herman
Kuipers, Ernst J.
Siersema, Peter D.
Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus
title Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus
title_full Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus
title_fullStr Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus
title_full_unstemmed Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus
title_short Biomarkers for Risk Stratification of Neoplastic Progression in Barrett Esophagus
title_sort biomarkers for risk stratification of neoplastic progression in barrett esophagus
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618977/
https://www.ncbi.nlm.nih.gov/pubmed/18032827
http://dx.doi.org/10.1155/2007/814950
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