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Clinicopathological significance of claudin-4 in gastric carcinoma

BACKGROUND: Aberrant expression of claudin proteins has been reported in a variety of cancers. Previous studies have demonstrated that overexpression of claudin may promote tumorigenesis and metastasis through increased invasion and survival of tumor cells. However, the prognostic significance of cl...

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Autores principales: Zhu, Jin-Liang, Gao, Peng, Wang, Zhen-Ning, Song, Yong-Xi, Li, Ai-Lin, Xu, Ying-Ying, Wang, Mei-Xian, Xu, Hui-Mian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717126/
https://www.ncbi.nlm.nih.gov/pubmed/23822740
http://dx.doi.org/10.1186/1477-7819-11-150
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author Zhu, Jin-Liang
Gao, Peng
Wang, Zhen-Ning
Song, Yong-Xi
Li, Ai-Lin
Xu, Ying-Ying
Wang, Mei-Xian
Xu, Hui-Mian
author_facet Zhu, Jin-Liang
Gao, Peng
Wang, Zhen-Ning
Song, Yong-Xi
Li, Ai-Lin
Xu, Ying-Ying
Wang, Mei-Xian
Xu, Hui-Mian
author_sort Zhu, Jin-Liang
collection PubMed
description BACKGROUND: Aberrant expression of claudin proteins has been reported in a variety of cancers. Previous studies have demonstrated that overexpression of claudin may promote tumorigenesis and metastasis through increased invasion and survival of tumor cells. However, the prognostic significance of claudin-4 in gastric cancer remains unclear. METHODS: Immunohistochemistry was used to analyze the expression of claudin-4 in 329 clinical gastric cancer specimens and 44 normal stomach samples, 21 intestinal metaplasia samples, and 21 adjacent precursor lesions dysplasia samples. Statistical analysis methods were used to evaluate the relationship between claudin-4 expression and various clinicopathological parameters. Univariate and multivariate analyses were performed, respectively, to detect the independent predictors of survival. RESULTS: Claudin-4 expression was present in only 7(15.9%) normal gastric samples, but expression of claudin-4 in the intestinal metaplasia lesions and dysplasia lesions was 90.5% and 95.2%, respectively. The expression of claudin-4 was significantly associated with histological differentiation (P < 0.001) and tumor growth patterns (P < 0.001) but not associated with patient survival. However, intermediate type staining of claudin-4 exhibited a trend of correlation with patients’ survival (P = 0.023). The five-year survival rate with low expression of claudin-4 in intermediate type (76.4%) was similar to expanding type (64.5%), while the high expression group (46.6%) was closer to infiltrative type (50.7%). CONCLUSIONS: The findings in this study demonstrate claudin-4 aberrant expression in gastric cancer and precursor lesions. The expression of claudin-4 could serve as a basis for identifying gastric cancer of the intermediate type.
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spelling pubmed-37171262013-07-21 Clinicopathological significance of claudin-4 in gastric carcinoma Zhu, Jin-Liang Gao, Peng Wang, Zhen-Ning Song, Yong-Xi Li, Ai-Lin Xu, Ying-Ying Wang, Mei-Xian Xu, Hui-Mian World J Surg Oncol Research BACKGROUND: Aberrant expression of claudin proteins has been reported in a variety of cancers. Previous studies have demonstrated that overexpression of claudin may promote tumorigenesis and metastasis through increased invasion and survival of tumor cells. However, the prognostic significance of claudin-4 in gastric cancer remains unclear. METHODS: Immunohistochemistry was used to analyze the expression of claudin-4 in 329 clinical gastric cancer specimens and 44 normal stomach samples, 21 intestinal metaplasia samples, and 21 adjacent precursor lesions dysplasia samples. Statistical analysis methods were used to evaluate the relationship between claudin-4 expression and various clinicopathological parameters. Univariate and multivariate analyses were performed, respectively, to detect the independent predictors of survival. RESULTS: Claudin-4 expression was present in only 7(15.9%) normal gastric samples, but expression of claudin-4 in the intestinal metaplasia lesions and dysplasia lesions was 90.5% and 95.2%, respectively. The expression of claudin-4 was significantly associated with histological differentiation (P < 0.001) and tumor growth patterns (P < 0.001) but not associated with patient survival. However, intermediate type staining of claudin-4 exhibited a trend of correlation with patients’ survival (P = 0.023). The five-year survival rate with low expression of claudin-4 in intermediate type (76.4%) was similar to expanding type (64.5%), while the high expression group (46.6%) was closer to infiltrative type (50.7%). CONCLUSIONS: The findings in this study demonstrate claudin-4 aberrant expression in gastric cancer and precursor lesions. The expression of claudin-4 could serve as a basis for identifying gastric cancer of the intermediate type. BioMed Central 2013-07-04 /pmc/articles/PMC3717126/ /pubmed/23822740 http://dx.doi.org/10.1186/1477-7819-11-150 Text en Copyright ©2013 Zhu 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
Zhu, Jin-Liang
Gao, Peng
Wang, Zhen-Ning
Song, Yong-Xi
Li, Ai-Lin
Xu, Ying-Ying
Wang, Mei-Xian
Xu, Hui-Mian
Clinicopathological significance of claudin-4 in gastric carcinoma
title Clinicopathological significance of claudin-4 in gastric carcinoma
title_full Clinicopathological significance of claudin-4 in gastric carcinoma
title_fullStr Clinicopathological significance of claudin-4 in gastric carcinoma
title_full_unstemmed Clinicopathological significance of claudin-4 in gastric carcinoma
title_short Clinicopathological significance of claudin-4 in gastric carcinoma
title_sort clinicopathological significance of claudin-4 in gastric carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717126/
https://www.ncbi.nlm.nih.gov/pubmed/23822740
http://dx.doi.org/10.1186/1477-7819-11-150
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