The expression of Claudin 1 correlates with β-catenin and is a prognostic factor of poor outcome in gastric cancer

45Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

Abstract

Claudin 1 is one of the tight junction proteins, which are critical in the maintenance of epithelial integrity. Aberrant regulation of CLDN1 and its correlation with β-catenin have been discovered in malignant tumors. The present study aimed to investigate the expression profile and clinical relevance of CLDN1 and β-catenin. The protein levels of CLDN1 and β-catenin were examined using immunohistochemical staining. The characteristics of expression profile and prognostic value were analyzed using Pearson's χ2 test and Kaplan-Meier analysis, respectively. β-catenin overexpression and knockdown were used to investigate its role in regulating CLDN1 expression. We showed that CLDN1 was overexpressed in intestinal-type, presence of lymph node metastasis, higher TNM stage in gastric cancer patients and correlated with decreased overall survival. The characteristics of CLDN1 expression were associated with that of β-catenin. CLDN1 and β-catenin showed similar prognostic value in intestinal-type gastric cancers. β-catenin knockdown and overexpression in cell models revealed a positive relation between CLDN1 and β-catenin. Our study demonstrated that CLDN1 is a biomarker for intestinal-type gastric cancer with shorter survival. The expression of CLDN1 was strongly associated with β-catenin in gastric cancer patients and a gastric cancer cell model.

Author supplied keywords

Cite

CITATION STYLE

APA

Huang, J., Li, J., Qu, Y., Zhang, J., Zhang, L., Chen, X., … Zhu, Z. (2014). The expression of Claudin 1 correlates with β-catenin and is a prognostic factor of poor outcome in gastric cancer. International Journal of Oncology, 44(4), 1293–1301. https://doi.org/10.3892/ijo.2014.2298

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free