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The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study

OBJECTIVES: The prognostic significance of chemokine receptors in stage I/II colon cancer is unclear. We assessed the prognostic value of chemokine receptor CXCR3 and CXCR4 in stage I/II colon cancer. METHODS: 145 patients with stage I/II colon cancer who underwent curative surgery alone from 2000 t...

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Autores principales: Du, Changzheng, Yao, Yunfeng, Xue, Weicheng, Zhu, Wei-Guo, Peng, Yifan, Gu, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139647/
https://www.ncbi.nlm.nih.gov/pubmed/25232565
http://dx.doi.org/10.1136/bmjopen-2014-005012
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author Du, Changzheng
Yao, Yunfeng
Xue, Weicheng
Zhu, Wei-Guo
Peng, Yifan
Gu, Jin
author_facet Du, Changzheng
Yao, Yunfeng
Xue, Weicheng
Zhu, Wei-Guo
Peng, Yifan
Gu, Jin
author_sort Du, Changzheng
collection PubMed
description OBJECTIVES: The prognostic significance of chemokine receptors in stage I/II colon cancer is unclear. We assessed the prognostic value of chemokine receptor CXCR3 and CXCR4 in stage I/II colon cancer. METHODS: 145 patients with stage I/II colon cancer who underwent curative surgery alone from 2000 to 2007 were investigated. Chemokine receptor expression was assessed by immunohistochemistry. The associations between CXCR3, CXCR4 and clinicopathological variables were analysed using the χ(2) test, and the relationships between chemokine receptors and a 5-year disease-free survival were analysed by univariate and multivariate analyses. RESULTS: The high-expression rates of CXCR3 and CXCR4 were 17.9% (26/145) and 38.6% (56/145), respectively. There were no significant associations between the expressions of CXCR3, CXCR4 and clinicopathological factors including gender, age, tumour location, histological differentiation, pathological stage, lymphovascular invasion and pretreatment serum carcinoembryonic antigen (CEA). The 5-year disease-free survival was not significantly different between low-expression groups and high-expression groups of CXCR3 and CXCR4. Multivariate analysis revealed that serum CEA and a number of retrieved lymph nodes, rather than chemokine receptors, were independent prognosticators. CONCLUSIONS: CXCR3 and CXCR4 are not independent prognosticators for stage I/II colon cancer after curative surgery.
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spelling pubmed-41396472014-08-25 The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study Du, Changzheng Yao, Yunfeng Xue, Weicheng Zhu, Wei-Guo Peng, Yifan Gu, Jin BMJ Open Pathology OBJECTIVES: The prognostic significance of chemokine receptors in stage I/II colon cancer is unclear. We assessed the prognostic value of chemokine receptor CXCR3 and CXCR4 in stage I/II colon cancer. METHODS: 145 patients with stage I/II colon cancer who underwent curative surgery alone from 2000 to 2007 were investigated. Chemokine receptor expression was assessed by immunohistochemistry. The associations between CXCR3, CXCR4 and clinicopathological variables were analysed using the χ(2) test, and the relationships between chemokine receptors and a 5-year disease-free survival were analysed by univariate and multivariate analyses. RESULTS: The high-expression rates of CXCR3 and CXCR4 were 17.9% (26/145) and 38.6% (56/145), respectively. There were no significant associations between the expressions of CXCR3, CXCR4 and clinicopathological factors including gender, age, tumour location, histological differentiation, pathological stage, lymphovascular invasion and pretreatment serum carcinoembryonic antigen (CEA). The 5-year disease-free survival was not significantly different between low-expression groups and high-expression groups of CXCR3 and CXCR4. Multivariate analysis revealed that serum CEA and a number of retrieved lymph nodes, rather than chemokine receptors, were independent prognosticators. CONCLUSIONS: CXCR3 and CXCR4 are not independent prognosticators for stage I/II colon cancer after curative surgery. BMJ Publishing Group 2014-08-13 /pmc/articles/PMC4139647/ /pubmed/25232565 http://dx.doi.org/10.1136/bmjopen-2014-005012 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Pathology
Du, Changzheng
Yao, Yunfeng
Xue, Weicheng
Zhu, Wei-Guo
Peng, Yifan
Gu, Jin
The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study
title The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study
title_full The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study
title_fullStr The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study
title_full_unstemmed The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study
title_short The expression of chemokine receptors CXCR3 and CXCR4 in predicting postoperative tumour progression in stages I-II colon cancer: a retrospective study
title_sort expression of chemokine receptors cxcr3 and cxcr4 in predicting postoperative tumour progression in stages i-ii colon cancer: a retrospective study
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139647/
https://www.ncbi.nlm.nih.gov/pubmed/25232565
http://dx.doi.org/10.1136/bmjopen-2014-005012
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