Evidence map›Paper›PMID 40844663›Full record

ArticleJournal of molecular histology2025

Hippo signaling pathway in human testis and seminoma: anticancer effect of verteporfin on human seminoma TCam-2 cells.

Tugce Onel, Basak Aru, Ecem Yildirim, Gulderen Yanikkaya Demirel, Sevim Baykal Koca, Aylin Yaba

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Article in Journal of molecular histology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Tugce OnelDepartment of Histology and Embryology, Faculty of Medicine, Demiroğlu Bilim University, 34394, Istanbul, Turkey.
Basak AruDepartment of Immunology, Yeditepe University Faculty of Medicine, 34755, Istanbul, Turkey.
Ecem YildirimDepartment of Histology and Embryology, Faculty of Medicine, University of Health Sciences, 34668, Istanbul, Turkey.
Gulderen Yanikkaya DemirelDepartment of Immunology, Yeditepe University Faculty of Medicine, 34755, Istanbul, Turkey.
Sevim Baykal KocaDepartment of Pathology, Samatya Education and Research Hospital, Istanbul, Turkey.
Aylin YabaDepartment of Histology and Embryology, Yeditepe University Faculty of Medicine, 34755, Istanbul, Turkey. aylinyaba@hotmail.com.ORCID http://orcid.org/0000-0001-6781-9983

Funding

Yeditepe University Research Projects and Scientific Activities of Yeditepe University (YAP) HD-22002
6 · The paper itself

Abstract

aimSeminoma and embryonal carcinoma are among the most common germ cell tumors. Verteporfin, a YAP-TEAD inhibitor, has emerged as a potential anticancer agent. This study investigated the localization of Hippo signaling proteins in human testis, seminoma, and non-seminoma tissues, and examined verteporfin’s effects on TCam-2 seminoma cells.

methodsProtein localization in tissues was assessed using immunohistochemistry. TCam-2 cells were treated with various concentrations of verteporfin (1–40 µM) for 24, 48, and 72 h. Protein and gene expression were analyzed via immunofluorescence, western blotting, and qRT-PCR.

resultsHippo pathway proteins showed distinct localization patterns across tissue types. Verteporfin treatment caused a dose- and time-dependent decrease in protein levels without altering mRNA expression. It also induced nuclear-to-cytoplasmic translocation of pathway proteins and reduced cell proliferation, migration, and viability, while simultaneously promoting apoptosis in TCam-2 human seminoma cells.

conclusionVerteporfin may serve as a promising therapeutic strategy for seminoma by targeting Hippo signaling. These findings support its potential role in personalized treatment approaches for testicular cancer.

Indexed as

Antineoplastic AgentsProtein Serine-Threonine KinasesSeminomaSignal TransductionTesticular NeoplasmsTestisVerteporfinApoptosisCell Line, TumorCell MovementCell ProliferationCell SurvivalGene Expression Regulation, NeoplasticHippo Signaling PathwayHumansMaleAntineoplastic AgentsProtein Serine-Threonine KinasesVerteporfinHippoHuman testisSeminomaTCam-2Verteporfin

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.