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CXCR7 expression in esophageal cancer
BACKGROUND: The chemokine CXCL12 and its receptor CXCR4 play a major role in tumor invasion, proliferation and metastasis in different malignant diseases, including esophageal carcinoma, amongst others. CXCR7 was recently identified as a novel alternate receptor for CXCL12. The aim of this study was...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851264/ https://www.ncbi.nlm.nih.gov/pubmed/24074251 http://dx.doi.org/10.1186/1479-5876-11-238 |
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author | Tachezy, Michael Zander, Hilke Gebauer, Florian von Loga, Katharina Pantel, Klaus Izbicki, Jakob R Bockhorn, Maximilian |
author_facet | Tachezy, Michael Zander, Hilke Gebauer, Florian von Loga, Katharina Pantel, Klaus Izbicki, Jakob R Bockhorn, Maximilian |
author_sort | Tachezy, Michael |
collection | PubMed |
description | BACKGROUND: The chemokine CXCL12 and its receptor CXCR4 play a major role in tumor invasion, proliferation and metastasis in different malignant diseases, including esophageal carcinoma, amongst others. CXCR7 was recently identified as a novel alternate receptor for CXCL12. The aim of this study was to evaluate the prognostic impact of expression of chemokine receptor CXCR7 in patients with esophageal carcinoma (EC). METHODS: Expression of CXCR7 in primary tumors, lymph nodes and distant metastases of 299 patients with EC was evaluated by immunohistochemistry on a tissue microarray and compared with clinical and histopathological data. RESULTS: In esophageal cancer sections, CXCR7-specific reactivity was apparent in 45% of the squamous cell carcinomas (ESCC), but only occasionally in adenocarcinomas. No correlation between CXCR4 and CXCR7 expression was evident. We correlated expression with clinical and histopathological characteristics, but could not find any association. CONCLUSIONS: Contrary to the other known CXCL12 receptor, CXCR4, CXCR7 is expressed in ESCC only, underlining the divergent mechanisms and backgrounds of EAC and ESCC. The results of the study do not indicate a significant functional role for CXCR7 in EAC or ESCC of the esophagus. However, its variable expression in the main two main types of EC needs to be further investigated. |
format | Online Article Text |
id | pubmed-3851264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38512642013-12-06 CXCR7 expression in esophageal cancer Tachezy, Michael Zander, Hilke Gebauer, Florian von Loga, Katharina Pantel, Klaus Izbicki, Jakob R Bockhorn, Maximilian J Transl Med Research BACKGROUND: The chemokine CXCL12 and its receptor CXCR4 play a major role in tumor invasion, proliferation and metastasis in different malignant diseases, including esophageal carcinoma, amongst others. CXCR7 was recently identified as a novel alternate receptor for CXCL12. The aim of this study was to evaluate the prognostic impact of expression of chemokine receptor CXCR7 in patients with esophageal carcinoma (EC). METHODS: Expression of CXCR7 in primary tumors, lymph nodes and distant metastases of 299 patients with EC was evaluated by immunohistochemistry on a tissue microarray and compared with clinical and histopathological data. RESULTS: In esophageal cancer sections, CXCR7-specific reactivity was apparent in 45% of the squamous cell carcinomas (ESCC), but only occasionally in adenocarcinomas. No correlation between CXCR4 and CXCR7 expression was evident. We correlated expression with clinical and histopathological characteristics, but could not find any association. CONCLUSIONS: Contrary to the other known CXCL12 receptor, CXCR4, CXCR7 is expressed in ESCC only, underlining the divergent mechanisms and backgrounds of EAC and ESCC. The results of the study do not indicate a significant functional role for CXCR7 in EAC or ESCC of the esophagus. However, its variable expression in the main two main types of EC needs to be further investigated. BioMed Central 2013-09-30 /pmc/articles/PMC3851264/ /pubmed/24074251 http://dx.doi.org/10.1186/1479-5876-11-238 Text en Copyright © 2013 Tachezy et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Tachezy, Michael Zander, Hilke Gebauer, Florian von Loga, Katharina Pantel, Klaus Izbicki, Jakob R Bockhorn, Maximilian CXCR7 expression in esophageal cancer |
title | CXCR7 expression in esophageal cancer |
title_full | CXCR7 expression in esophageal cancer |
title_fullStr | CXCR7 expression in esophageal cancer |
title_full_unstemmed | CXCR7 expression in esophageal cancer |
title_short | CXCR7 expression in esophageal cancer |
title_sort | cxcr7 expression in esophageal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851264/ https://www.ncbi.nlm.nih.gov/pubmed/24074251 http://dx.doi.org/10.1186/1479-5876-11-238 |
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