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Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas
INTRODUCTION: The tight junction molecule Claudin 18.2 is selectively expressed in healthy and malignant gastric epithelial tissue and is a promising therapy target for high Claudin 18.2 expressing adenocarcinomas of the esophagogastric junction and stomach (AEG/S). METHODS: This study analyzed the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577914/ https://www.ncbi.nlm.nih.gov/pubmed/32488802 http://dx.doi.org/10.1007/s12094-020-02380-0 |
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author | Arnold, A. Daum, S. von Winterfeld, M. Berg, E. Hummel, M. Rau, B. Stein, U. Treese, C. |
author_facet | Arnold, A. Daum, S. von Winterfeld, M. Berg, E. Hummel, M. Rau, B. Stein, U. Treese, C. |
author_sort | Arnold, A. |
collection | PubMed |
description | INTRODUCTION: The tight junction molecule Claudin 18.2 is selectively expressed in healthy and malignant gastric epithelial tissue and is a promising therapy target for high Claudin 18.2 expressing adenocarcinomas of the esophagogastric junction and stomach (AEG/S). METHODS: This study analyzed the prevalence, characteristics and prognostic impact of Claudin 18.2 expression in primary tumor, lymph node and distant metastasis in a large Caucasian AGE/S cohort with 414 patients. RESULTS: Claudin 18.2 was highly expressed in 17.1% of primary tumors, 26.7% of lymph node metastasis and 16.7% of distant metastasis. High Claudin 18.2 expression in lymph node metastasis and primary tumors correlated significantly (p < 0.001). High expression of Claudin 18.2 was neither associated with histomorphogical subtype, or tumor state, nor with overall survival. CONCLUSION: In Caucasian AEG/S patients, 17.1% appeared to be eligible for an anti-Claudin 18.2 therapy. Claudin 18.2 expression itself has no impact on prognosis and is not related to any tumor subtype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12094-020-02380-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7577914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-75779142020-10-27 Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas Arnold, A. Daum, S. von Winterfeld, M. Berg, E. Hummel, M. Rau, B. Stein, U. Treese, C. Clin Transl Oncol Brief Research Article INTRODUCTION: The tight junction molecule Claudin 18.2 is selectively expressed in healthy and malignant gastric epithelial tissue and is a promising therapy target for high Claudin 18.2 expressing adenocarcinomas of the esophagogastric junction and stomach (AEG/S). METHODS: This study analyzed the prevalence, characteristics and prognostic impact of Claudin 18.2 expression in primary tumor, lymph node and distant metastasis in a large Caucasian AGE/S cohort with 414 patients. RESULTS: Claudin 18.2 was highly expressed in 17.1% of primary tumors, 26.7% of lymph node metastasis and 16.7% of distant metastasis. High Claudin 18.2 expression in lymph node metastasis and primary tumors correlated significantly (p < 0.001). High expression of Claudin 18.2 was neither associated with histomorphogical subtype, or tumor state, nor with overall survival. CONCLUSION: In Caucasian AEG/S patients, 17.1% appeared to be eligible for an anti-Claudin 18.2 therapy. Claudin 18.2 expression itself has no impact on prognosis and is not related to any tumor subtype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12094-020-02380-0) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-06-01 2020 /pmc/articles/PMC7577914/ /pubmed/32488802 http://dx.doi.org/10.1007/s12094-020-02380-0 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Brief Research Article Arnold, A. Daum, S. von Winterfeld, M. Berg, E. Hummel, M. Rau, B. Stein, U. Treese, C. Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas |
title | Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas |
title_full | Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas |
title_fullStr | Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas |
title_full_unstemmed | Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas |
title_short | Prognostic impact of Claudin 18.2 in gastric and esophageal adenocarcinomas |
title_sort | prognostic impact of claudin 18.2 in gastric and esophageal adenocarcinomas |
topic | Brief Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577914/ https://www.ncbi.nlm.nih.gov/pubmed/32488802 http://dx.doi.org/10.1007/s12094-020-02380-0 |
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