Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Tachezy, Michael, Zander, Hilke, Gebauer, Florian, von Loga, Katharina, Pantel, Klaus, Izbicki, Jakob R, Bockhorn, Maximilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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
_version_ 1782294257409720320
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
work_keys_str_mv AT tachezymichael cxcr7expressioninesophagealcancer
AT zanderhilke cxcr7expressioninesophagealcancer
AT gebauerflorian cxcr7expressioninesophagealcancer
AT vonlogakatharina cxcr7expressioninesophagealcancer
AT pantelklaus cxcr7expressioninesophagealcancer
AT izbickijakobr cxcr7expressioninesophagealcancer
AT bockhornmaximilian cxcr7expressioninesophagealcancer