Differential Expression Patterns of Bcl-2, D2-40, β-Catenin and E-Cadherin in Thymomas: Correlation with Clinical Stages and Subtypes

胸腺瘤 免疫组织化学 病理 染色 鉴别诊断 临床意义 医学 阶段(地层学) 生物 古生物学
作者
Büşra Yaprak Bayrak,Ayşegül Üçüncü Kefeli,Çiğdem Vural,İsa Çam,Ekin Y. Calcali,Aykut Eliçora,Hüseyin Fatih Sezer,Salih Topçu
出处
期刊:Applied Immunohistochemistry & Molecular Morphology [Lippincott Williams & Wilkins]
卷期号:33 (4): 250-256
标识
DOI:10.1097/pai.0000000000001264
摘要

Thymomas are rare mediastinal tumors exhibiting heterogeneous behavior. Although histologic subtypes and stages serve as prognostic factors, the molecular mechanisms of thymoma progression are unclear. Immunohistochemical markers like Bcl-2, D2-40, β-catenin, and E-cadherin offer insights into thymoma biology, but their predictive value for clinical outcomes remains uncertain. This study evaluated the expression of these markers across thymoma subtypes and stages, aiming to assess their prognostic significance. A retrospective analysis was conducted on 66 thymoma cases resected at a single center between 2005 and 2023. Immunohistochemical staining was performed to assess the expression of Bcl-2, D2-40, β-catenin, and E-cadherin. Clinicopathological characteristics were correlated with immunohistochemical findings using statistical analysis. Differential expression patterns of Bcl-2, D2-40, β-catenin, and E-cadherin were observed across thymoma subtypes and clinical stages. Bcl-2 displayed cytoplasmic positivity predominantly in type A and B thymomas, while E-cadherin showed membranous staining in type B thymomas and cytoplasmic staining in type A and AB thymomas. β-catenin demonstrated membranous staining in type B thymomas and cytoplasmic staining in type A and AB thymomas. D2-40 expression was localized to peripheral regions and invasive nests of thymomas, with higher expression in type B2 thymomas and early-stage tumors. Our findings indicate that immunohistochemical markers may provide valuable insights into thymoma biology and prognosis. Further validation in larger, multicenter cohorts is warranted to confirm the prognostic significance of these markers and their potential utility in guiding clinical management.

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