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Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis

BACKGROUND: The prognostic significance of claudin 4 (CLDN4) in patients with gastric cancer (GC) is controversial. This meta-analysis aims to assess the correlation between CLDN4 expression and clinicopathological characteristics and assess the prognostic significance of CLDN4 in GC. METHODS: We se...

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Autores principales: Chen, Xiaowan, Zhao, Junhua, Li, Ailin, Gao, Peng, Sun, Jingxu, Song, Yongxi, Liu, Jingjing, Chen, Ping, Wang, Zhenning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892849/
https://www.ncbi.nlm.nih.gov/pubmed/27313466
http://dx.doi.org/10.2147/OTT.S99461
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author Chen, Xiaowan
Zhao, Junhua
Li, Ailin
Gao, Peng
Sun, Jingxu
Song, Yongxi
Liu, Jingjing
Chen, Ping
Wang, Zhenning
author_facet Chen, Xiaowan
Zhao, Junhua
Li, Ailin
Gao, Peng
Sun, Jingxu
Song, Yongxi
Liu, Jingjing
Chen, Ping
Wang, Zhenning
author_sort Chen, Xiaowan
collection PubMed
description BACKGROUND: The prognostic significance of claudin 4 (CLDN4) in patients with gastric cancer (GC) is controversial. This meta-analysis aims to assess the correlation between CLDN4 expression and clinicopathological characteristics and assess the prognostic significance of CLDN4 in GC. METHODS: We searched the PubMed and Embase databases. We performed the meta-analysis with odds ratio (OR), hazard ratio (HR), and 95% confidence interval (CI) as effect values. RESULTS: Fourteen studies containing 2,106 patients with GC were analyzed. The overall analysis showed that CLDN4 expression was associated with increasing pT category, tumor size, and lymph node metastasis in patients with GC (pT3–T4 vs pT1–T2: OR =1.56, 95% CI =1.13–2.16; P<0.01; large tumor size vs small tumor size: OR =1.64, 95% CI =1.15–2.34; P<0.01; positive lymph node metastasis vs negative lymph node metastasis: OR =1.49, 95% CI =1.12–1.97; P<0.01). CLDN4 expression was associated with histological differentiation (differentiated type vs undifferentiated type: OR =2.90, 95% CI =1.32–6.37; P=0.01; Lauren intestinal type vs diffuse type: OR =3.51, 95% CI =1.48–8.28; P<0.01). CLDN4 expression was also strongly associated with sex and age. This meta-analysis found no significant association between CLDN4 expression and prognosis for overall survival in patients with GC (HR =0.74, 95% CI =0.43–1.27; P=0.28). CONCLUSION: Present study indicates that aberrant CLDN4 expression plays an important role in the clinicopathological characteristics of GC.
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spelling pubmed-48928492016-06-16 Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis Chen, Xiaowan Zhao, Junhua Li, Ailin Gao, Peng Sun, Jingxu Song, Yongxi Liu, Jingjing Chen, Ping Wang, Zhenning Onco Targets Ther Original Research BACKGROUND: The prognostic significance of claudin 4 (CLDN4) in patients with gastric cancer (GC) is controversial. This meta-analysis aims to assess the correlation between CLDN4 expression and clinicopathological characteristics and assess the prognostic significance of CLDN4 in GC. METHODS: We searched the PubMed and Embase databases. We performed the meta-analysis with odds ratio (OR), hazard ratio (HR), and 95% confidence interval (CI) as effect values. RESULTS: Fourteen studies containing 2,106 patients with GC were analyzed. The overall analysis showed that CLDN4 expression was associated with increasing pT category, tumor size, and lymph node metastasis in patients with GC (pT3–T4 vs pT1–T2: OR =1.56, 95% CI =1.13–2.16; P<0.01; large tumor size vs small tumor size: OR =1.64, 95% CI =1.15–2.34; P<0.01; positive lymph node metastasis vs negative lymph node metastasis: OR =1.49, 95% CI =1.12–1.97; P<0.01). CLDN4 expression was associated with histological differentiation (differentiated type vs undifferentiated type: OR =2.90, 95% CI =1.32–6.37; P=0.01; Lauren intestinal type vs diffuse type: OR =3.51, 95% CI =1.48–8.28; P<0.01). CLDN4 expression was also strongly associated with sex and age. This meta-analysis found no significant association between CLDN4 expression and prognosis for overall survival in patients with GC (HR =0.74, 95% CI =0.43–1.27; P=0.28). CONCLUSION: Present study indicates that aberrant CLDN4 expression plays an important role in the clinicopathological characteristics of GC. Dove Medical Press 2016-05-27 /pmc/articles/PMC4892849/ /pubmed/27313466 http://dx.doi.org/10.2147/OTT.S99461 Text en © 2016 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Chen, Xiaowan
Zhao, Junhua
Li, Ailin
Gao, Peng
Sun, Jingxu
Song, Yongxi
Liu, Jingjing
Chen, Ping
Wang, Zhenning
Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis
title Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis
title_full Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis
title_fullStr Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis
title_full_unstemmed Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis
title_short Clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis
title_sort clinicopathological significance of claudin 4 expression in gastric carcinoma: a systematic review and meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892849/
https://www.ncbi.nlm.nih.gov/pubmed/27313466
http://dx.doi.org/10.2147/OTT.S99461
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