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Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis

BACKGROUND: Syndecan-1 plays a vital role in the suppression, transformation, and migration of several cancer types, including colorectal cancer (CRC). However, the prognostic and clinical significance of syndecan-1 in CRC remains conflicting. Therefore, we performed a meta-analysis to clarify this...

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Autores principales: Wei, Hao-tang, Guo, Er-na, Dong, Bao-guo, Chen, Li-sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628393/
https://www.ncbi.nlm.nih.gov/pubmed/26518017
http://dx.doi.org/10.1186/s12876-015-0383-2
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author Wei, Hao-tang
Guo, Er-na
Dong, Bao-guo
Chen, Li-sheng
author_facet Wei, Hao-tang
Guo, Er-na
Dong, Bao-guo
Chen, Li-sheng
author_sort Wei, Hao-tang
collection PubMed
description BACKGROUND: Syndecan-1 plays a vital role in the suppression, transformation, and migration of several cancer types, including colorectal cancer (CRC). However, the prognostic and clinical significance of syndecan-1 in CRC remains conflicting. Therefore, we performed a meta-analysis to clarify this relationship. METHODS: A comprehensive literature search for relevant studies published up to December 2014 was performed using PubMed, EMBASE, and Ovid library database. The odds ratio (OR) and pooled hazard ratio (HR) with their 95 % confidence intervals (CI) were used to estimate the effects. RESULTS: Ten studies with 888 CRC patients were selected for evaluation. The results showed that syndecan-1 expression was lower in CRC tissue than in normal colorectal tissue (OR = 0.02, 95 % CI = 0.00–0.09), and lower in the advanced stage than in the early stage (OR = 2.24, 95 % CI = 1.14 − 4.42). Additionally, syndecan-1 expression was higher in well and moderately differentiated CRC than in poorly differentiated CRC (OR = 2.91, 95 % CI = 1.21–6.98); no significant difference was found in patients with or without lymph node metastasis (OR = 0.91, 95 % CI = 0.34–2.43) and distant metastasis (OR = 0.89, 95 % CI = 0.19-4.21). The pooled results showed that syndecan-1 expression was not associated with survival in CRC patients (HR = 0.93, 95 % CI = 0.86–1.01). CONCLUSION: This meta-analysis indicated that loss of syndecan-1 expression is associated with CRC development, histological differentiation, and clinical stage, but not with lymph node metastasis and distant metastasis. In addition, these findings fail to support the prognostic significance of syndecan-1 in CRC.
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spelling pubmed-46283932015-11-01 Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis Wei, Hao-tang Guo, Er-na Dong, Bao-guo Chen, Li-sheng BMC Gastroenterol Research Article BACKGROUND: Syndecan-1 plays a vital role in the suppression, transformation, and migration of several cancer types, including colorectal cancer (CRC). However, the prognostic and clinical significance of syndecan-1 in CRC remains conflicting. Therefore, we performed a meta-analysis to clarify this relationship. METHODS: A comprehensive literature search for relevant studies published up to December 2014 was performed using PubMed, EMBASE, and Ovid library database. The odds ratio (OR) and pooled hazard ratio (HR) with their 95 % confidence intervals (CI) were used to estimate the effects. RESULTS: Ten studies with 888 CRC patients were selected for evaluation. The results showed that syndecan-1 expression was lower in CRC tissue than in normal colorectal tissue (OR = 0.02, 95 % CI = 0.00–0.09), and lower in the advanced stage than in the early stage (OR = 2.24, 95 % CI = 1.14 − 4.42). Additionally, syndecan-1 expression was higher in well and moderately differentiated CRC than in poorly differentiated CRC (OR = 2.91, 95 % CI = 1.21–6.98); no significant difference was found in patients with or without lymph node metastasis (OR = 0.91, 95 % CI = 0.34–2.43) and distant metastasis (OR = 0.89, 95 % CI = 0.19-4.21). The pooled results showed that syndecan-1 expression was not associated with survival in CRC patients (HR = 0.93, 95 % CI = 0.86–1.01). CONCLUSION: This meta-analysis indicated that loss of syndecan-1 expression is associated with CRC development, histological differentiation, and clinical stage, but not with lymph node metastasis and distant metastasis. In addition, these findings fail to support the prognostic significance of syndecan-1 in CRC. BioMed Central 2015-10-30 /pmc/articles/PMC4628393/ /pubmed/26518017 http://dx.doi.org/10.1186/s12876-015-0383-2 Text en © Wei et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wei, Hao-tang
Guo, Er-na
Dong, Bao-guo
Chen, Li-sheng
Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis
title Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis
title_full Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis
title_fullStr Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis
title_full_unstemmed Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis
title_short Prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis
title_sort prognostic and clinical significance of syndecan-1 in colorectal cancer: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628393/
https://www.ncbi.nlm.nih.gov/pubmed/26518017
http://dx.doi.org/10.1186/s12876-015-0383-2
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