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High Claudin-4 Antigen Expression in Triple-Negative Breast Cancer by the Immunohistochemistry Method Publisher



Naimi A1 ; Zare N1 ; Amjadi E2 ; Soltan M1
Authors
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Authors Affiliations
  1. 1. Department of Pathology, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Poursina Hakim Digestive Diseases Research Center, Isfahan, Iran

Source: Journal of Research in Medical Sciences Published:2022


Abstract

Background: Triple-negative breast cancer is a heterogeneous subtype of breast cancer. Claudin is an epithelial tight junctional protein, and also it is a receptor for clostridium perfringens enterotoxin and shows impairment of expression in several cancers. The chief purpose of this study is to assess the claudin-4 expression in triple-negative breast cancer (TNBC) Iranian patients and evaluate its correlation with some clinicopathological factors. Materials and Methods: In this study, 81 TNBC patients were evaluated for the claudin-4 expression by immunohistochemistry. The slides' staining intensity was examined and scored from 0 to 3. Then, slides were reviewed to assess the percentage of cells with membrane and cytoplasmic staining; the obtaining scores were 1-4. Finally, added the resulting two numbers from two stages, and the final number was a maximum of 7. Final scores of 0-3 were considered the low expression, and 4-7 were considered the high expression. Finally, the collected data were analyzed using the Chi-square test. Results: Eighty-one women with breast cancer and a mean age of 49 ± 12 years participated in the study. In 80% of the patients, there was a high expression of claudin-4 marker, and 20% had low expression. The expression level of the marker was not significantly correlated with age, tumor size, lymph node involvement, tumor grade, disease stage, Ki-67, and metastasis. Conclusion: The present study confirmed the high frequency of claudin-4 antigen expression in TNBC patients, and no significant correlation was observed between the expression of antigen and demographic or clinicopathological factors. © 2022 BMJ Publishing Group. All rights reserved.