Background & Objective: Basal cell carcinoma (BCC) is a common skin cancer arising from the basal layer of the epidermis and its appendages. They are locally invasive, aggressive, and destructive of skin and the surrounding structures. Β-Catenin is a multifunctional protein located to the intracellular side of the cytoplasmic membrane coded by the CTNNB1 gene, which maps to chromosome 3p22.1. It has a critical role in cell-to-cell adhesion by linking cadherins to the actin cytoskeleton and has a central role in transcriptional regulation in the Wnt signaling pathway. We evaluated the diagnostic value of the Beta catenin immunohistochemistry marker in distinction of aggressive and non-aggressive Basal cell carcinoma. Methods: This cross sectional and descriptive-analytical study was done on archived formalin fixed, paraffin embedded tissue blocks in pathology library of Al-Zahra hospital in Isfahan city. We used immunochemistry to determinate the role of Β-Catenin in aggressiveness in BCC with higher rate of relapse. Results: A total of 76 samples were evaluated in two groups (aggressive &none aggressive). The mean percentage of cytoplasmic Β-Catenin staining in aggressive group was more significant than the other group (sensitivity: 86.8% specificity: 81.6%, PPV: 81.5% and NPV: 86.1%) and the mean percentage of membranous Β-Catenin staining in non-aggressive group were significant more than the aggressive group. Intensity of membranous staining in both groups significant less than normal epithelium. Conclusion: Cytoplasmic Β-Catenin staining in aggressive BCC is more significant than non-aggressive subtypes, so this indicates that the use of Β-Catenin IHC marker maybe helpful in the diagnosis of aggressive BCC.
CITATION STYLE
Rajabi, P., Heydarpoor, M., Maghsoudi, A., Mohaghegh, F., & Mobarakeh, M. D. (2019). The study for diagnostic value of Β-catenin immunohistochemistry marker in distinction of aggressive and non-aggressive basal cell carcinoma. Iranian Journal of Pathology, 14(1), 52–60. https://doi.org/10.30699/IJP.14.1.52
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