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Nuclear Expression of β-Catenin Is Associated with Improved Outcomes in Endometrial Cancer. | LitMetric

Nuclear Expression of β-Catenin Is Associated with Improved Outcomes in Endometrial Cancer.

Diagnostics (Basel)

Division of Gynecologic Oncology, Department of Woman, Child and Public Health, Fondazione Policlinico Universitario A. Gemelli-IRCCS, Catholic University of Sacred Heart, 00168 Rome, Italy.

Published: October 2022

AI Article Synopsis

Article Abstract

Beta-catenin is involved in intercellular adhesion and participates in the Wnt signaling pathway. This study evaluated the expression pattern and prognostic value of β-catenin in a series of endometrial carcinoma patients. Immunohistochemical analyses were used to assess the expression and subcellular localization of β-catenin from tissue sections of 74 patients with endometrial carcinoma. No correlation was found between beta-catenin expression and clinicopathological parameters. Patients expressing nuclear β-catenin ( = 13; 16%) showed a more favorable prognosis than patients expressing membranous β-catenin; the 5-year disease-related survival rate was 100% for cases expressing nuclear β-catenin, compared with 73.8% (SE 0.08) of cases expressing membranous β-catenin ( = 0.04). Although statistical significance was not reached ( = 0.15), cases expressing nuclear β-catenin showed a 5-year disease-free survival rate of 90.9% (SE 0.08) compared with 67.4% (SE 0.08) of cases expressing membranous β-catenin. Univariate Cox analysis revealed that membranous β-catenin expression was found to be associated with a relative risk of death of 33.9 ( = 0.04). The stage of disease ( = 0.0006), histology ( = 0.003), and grading ( = 0.008) were also significantly correlated with disease-free survival according to univariate Cox analyses. Determining β-catenin expression and localization patterns may predict survival in patients with endometrial cancer and, therefore, should be considered a potential prognostic marker of disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600744PMC
http://dx.doi.org/10.3390/diagnostics12102401DOI Listing

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