Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminoma

IntroductionThe most common testicular tumors are seminomas. They are characterized by rapid growth and a very high potential for metastasis to other organs. Mutual interactions of tumor cells play an important role in the invasiveness and metastatic capacity, in which complexes of adhesion proteins...

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Main Authors: Grzegorz Młynarczyk, Natalia Domian, Irena Kasacka
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1269637/full
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author Grzegorz Młynarczyk
Natalia Domian
Irena Kasacka
author_facet Grzegorz Młynarczyk
Natalia Domian
Irena Kasacka
author_sort Grzegorz Młynarczyk
collection DOAJ
description IntroductionThe most common testicular tumors are seminomas. They are characterized by rapid growth and a very high potential for metastasis to other organs. Mutual interactions of tumor cells play an important role in the invasiveness and metastatic capacity, in which complexes of adhesion proteins play a special role. There is a lack of studies on changes in these molecules and their behaviour in testicular cancer. The aim of the study was immunohistochemical identification and evalutaion of adhesive molecules β-catenin, E-cadherin, galectin-3 in testicular cancer – seminoma.MethodsTests were performed on sections of testicular cancer – seminoma in comparison with unchanged tissue samples as a control. Material was taken from 30 patients who underwent orchiectomy. Immunohistochemistry and PCR were used to identify β-catenin, E-cadherin and galectin-3 and gene expression.ResultsImmunoreactivity and expression of β-catenin and E-cadherin in seminomas were markedly decreased compared to non-cancerous testicular tissue. Galectin-3 immunoreactivity was found in both control and cancerous tissue, but in different location. In non-cancerous tissue, it was localized in the cytoplasm of the cells of the seminiferous tubules, in seminomas it was localized mainly in the endothelium. The expression of the Lgals3 gene encoding galectin-3 in seminomas was slightl higher in relation to the tissue unchanged by the carcinogenetic process.ConclusionsThe results of the study suggest a significant role of β-catenin, E-cadherin and galectin-3 in the carcinogenesis of seminomas and may indicate new aspects of the patomechanism of seminomas formation, and thus time lead to better understand the biology of these tumors.
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spelling doaj.art-c60f2371fe1c47b8b7a9d21f1bbf593a2023-12-08T12:28:12ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2023-12-011310.3389/fonc.2023.12696371269637Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminomaGrzegorz Młynarczyk0Natalia Domian1Irena Kasacka2Department of Urology, Medical University of Białystok, Bialystok, PolandDepartment of Histology and Cytophysiology, Medical University of Białystok, Bialystok, PolandDepartment of Histology and Cytophysiology, Medical University of Białystok, Bialystok, PolandIntroductionThe most common testicular tumors are seminomas. They are characterized by rapid growth and a very high potential for metastasis to other organs. Mutual interactions of tumor cells play an important role in the invasiveness and metastatic capacity, in which complexes of adhesion proteins play a special role. There is a lack of studies on changes in these molecules and their behaviour in testicular cancer. The aim of the study was immunohistochemical identification and evalutaion of adhesive molecules β-catenin, E-cadherin, galectin-3 in testicular cancer – seminoma.MethodsTests were performed on sections of testicular cancer – seminoma in comparison with unchanged tissue samples as a control. Material was taken from 30 patients who underwent orchiectomy. Immunohistochemistry and PCR were used to identify β-catenin, E-cadherin and galectin-3 and gene expression.ResultsImmunoreactivity and expression of β-catenin and E-cadherin in seminomas were markedly decreased compared to non-cancerous testicular tissue. Galectin-3 immunoreactivity was found in both control and cancerous tissue, but in different location. In non-cancerous tissue, it was localized in the cytoplasm of the cells of the seminiferous tubules, in seminomas it was localized mainly in the endothelium. The expression of the Lgals3 gene encoding galectin-3 in seminomas was slightl higher in relation to the tissue unchanged by the carcinogenetic process.ConclusionsThe results of the study suggest a significant role of β-catenin, E-cadherin and galectin-3 in the carcinogenesis of seminomas and may indicate new aspects of the patomechanism of seminomas formation, and thus time lead to better understand the biology of these tumors.https://www.frontiersin.org/articles/10.3389/fonc.2023.1269637/fullβ-cateninE-cadheringalectin-3testicular cancerseminoma
spellingShingle Grzegorz Młynarczyk
Natalia Domian
Irena Kasacka
Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminoma
Frontiers in Oncology
β-catenin
E-cadherin
galectin-3
testicular cancer
seminoma
title Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminoma
title_full Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminoma
title_fullStr Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminoma
title_full_unstemmed Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminoma
title_short Changes in adhesion molecules: β-catenin, E-cadherin and Galectin-3 in cells of testicular seminoma
title_sort changes in adhesion molecules β catenin e cadherin and galectin 3 in cells of testicular seminoma
topic β-catenin
E-cadherin
galectin-3
testicular cancer
seminoma
url https://www.frontiersin.org/articles/10.3389/fonc.2023.1269637/full
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AT nataliadomian changesinadhesionmoleculesbcateninecadherinandgalectin3incellsoftesticularseminoma
AT irenakasacka changesinadhesionmoleculesbcateninecadherinandgalectin3incellsoftesticularseminoma