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Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer
PURPOSE: Experimental studies have suggested that the stromal-derived factor-1 (SDF-1)/CXCR4 axis is associated with tumor aggressiveness and metastasis in several malignancies. We performed a meta-analysis to elucidate the relationship between CXCR4 expression and the clinicopathological features o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Sexual Medicine and Andrology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298820/ https://www.ncbi.nlm.nih.gov/pubmed/25606566 http://dx.doi.org/10.5534/wjmh.2014.32.3.167 |
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author | Lee, Joo Yong Kang, Dong Hyuk Chung, Doo Yong Kwon, Jong Kyou Lee, Hyungmin Cho, Nam Hoon Choi, Young Deuk Hong, Sung Joon Cho, Kang Su |
author_facet | Lee, Joo Yong Kang, Dong Hyuk Chung, Doo Yong Kwon, Jong Kyou Lee, Hyungmin Cho, Nam Hoon Choi, Young Deuk Hong, Sung Joon Cho, Kang Su |
author_sort | Lee, Joo Yong |
collection | PubMed |
description | PURPOSE: Experimental studies have suggested that the stromal-derived factor-1 (SDF-1)/CXCR4 axis is associated with tumor aggressiveness and metastasis in several malignancies. We performed a meta-analysis to elucidate the relationship between CXCR4 expression and the clinicopathological features of prostate cancer. MATERIALS AND METHODS: Data were collected from studies comparing Gleason score, T stage, and the presence of metastasis with CXCR4 levels in human prostate cancer samples. The studies were pooled, and the odds ratio (OR) of CXCR4 expression for clinical and pathological variables was calculated. RESULTS: Five articles were eligible for the current meta-analysis. We found no relationship between CXCR4 expression and Gleason score (<7 vs. ≥7). The forest plot using the fixed-effects model indicated an OR of 1.585 (95% confidence interval [CI]: 0.793~3.171; p=0.193). Further, CXCR4 expression was not associated with the T stage (<T3 vs. ≥T3), and the relevant meta-analysis showed OR=1.803 (95% CI: 0.756~4.297, p=0.183). However, increased CXCR4 expression was strongly associated with metastatic disease with a fixed-effects pooled OR of 7.459 (95% CI: 2.665~20.878, p<0.001). CONCLUSIONS: Our meta-analysis showed that the higher CXCR4 protein expression in prostate cancer specimens is significantly associated with the presence of metastatic disease. This supports previous experimental data supporting the role played by the SDF-1/CXCR4 axis in metastasis. |
format | Online Article Text |
id | pubmed-4298820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korean Society for Sexual Medicine and Andrology |
record_format | MEDLINE/PubMed |
spelling | pubmed-42988202015-01-20 Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer Lee, Joo Yong Kang, Dong Hyuk Chung, Doo Yong Kwon, Jong Kyou Lee, Hyungmin Cho, Nam Hoon Choi, Young Deuk Hong, Sung Joon Cho, Kang Su World J Mens Health Original Article PURPOSE: Experimental studies have suggested that the stromal-derived factor-1 (SDF-1)/CXCR4 axis is associated with tumor aggressiveness and metastasis in several malignancies. We performed a meta-analysis to elucidate the relationship between CXCR4 expression and the clinicopathological features of prostate cancer. MATERIALS AND METHODS: Data were collected from studies comparing Gleason score, T stage, and the presence of metastasis with CXCR4 levels in human prostate cancer samples. The studies were pooled, and the odds ratio (OR) of CXCR4 expression for clinical and pathological variables was calculated. RESULTS: Five articles were eligible for the current meta-analysis. We found no relationship between CXCR4 expression and Gleason score (<7 vs. ≥7). The forest plot using the fixed-effects model indicated an OR of 1.585 (95% confidence interval [CI]: 0.793~3.171; p=0.193). Further, CXCR4 expression was not associated with the T stage (<T3 vs. ≥T3), and the relevant meta-analysis showed OR=1.803 (95% CI: 0.756~4.297, p=0.183). However, increased CXCR4 expression was strongly associated with metastatic disease with a fixed-effects pooled OR of 7.459 (95% CI: 2.665~20.878, p<0.001). CONCLUSIONS: Our meta-analysis showed that the higher CXCR4 protein expression in prostate cancer specimens is significantly associated with the presence of metastatic disease. This supports previous experimental data supporting the role played by the SDF-1/CXCR4 axis in metastasis. Korean Society for Sexual Medicine and Andrology 2014-12 2014-12-29 /pmc/articles/PMC4298820/ /pubmed/25606566 http://dx.doi.org/10.5534/wjmh.2014.32.3.167 Text en Copyright © 2014 Korean Society for Sexual Medicine and Andrology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Joo Yong Kang, Dong Hyuk Chung, Doo Yong Kwon, Jong Kyou Lee, Hyungmin Cho, Nam Hoon Choi, Young Deuk Hong, Sung Joon Cho, Kang Su Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer |
title | Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer |
title_full | Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer |
title_fullStr | Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer |
title_full_unstemmed | Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer |
title_short | Meta-Analysis of the Relationship between CXCR4 Expression and Metastasis in Prostate Cancer |
title_sort | meta-analysis of the relationship between cxcr4 expression and metastasis in prostate cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298820/ https://www.ncbi.nlm.nih.gov/pubmed/25606566 http://dx.doi.org/10.5534/wjmh.2014.32.3.167 |
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