Updating germ cell tumour pathogenesis - the ability of seminomas for FOXA2-driven extra-embryonic differentiation.


Journal

Histopathology
ISSN: 1365-2559
Titre abrégé: Histopathology
Pays: England
ID NLM: 7704136

Informations de publication

Date de publication:
Sep 2023
Historique:
revised: 06 04 2023
received: 03 03 2023
accepted: 16 04 2023
medline: 11 8 2023
pubmed: 2 6 2023
entrez: 2 6 2023
Statut: ppublish

Résumé

Testicular germ cell tumours are the most common solid malignancies in young men of age 14-44 years. It is generally accepted that both seminomas and non-seminomas arise from a common precursor, the germ cell neoplasia in-situ, which itself is the result of a defective (primordial) germ cell development. The stem cell-like population of the non-seminomas, the embryonal carcinoma, is capable of the differentiation of all three germ layers (teratomas) and extra-embryonic tissues (yolk-sac tumours, choriocarcioma) into cells. In contrast, seminomas are thought to have a limited differentiation potential. Nevertheless, several studies have highlighted their ability to undergo reprogramming to an embryonal carcinoma or differentiation into other non-seminomatous entities. Here, we demonstrate that in approximately 5% of seminomas, the yolk-sac tumour driver gene FOXA2 is detectable at the protein level, indicative of an occult yolk-sac tumour subpopulation that putatively arose from seminoma cells, as the presence of other GCT entities could be excluded. The presence of these subpopulations might render the tumour more aggressive and argue for an adjustment of the therapeutic concept. We used our data to update the model of germ cell tumour pathogenesis, especially regarding the developmental potential of seminomas. Additionally, we suggest to include detection of FOXA2 into standard routine diagnosis of seminomas.

Identifiants

pubmed: 37265221
doi: 10.1111/his.14933
doi:

Substances chimiques

FOXA2 protein, human 0
Hepatocyte Nuclear Factor 3-beta 135845-92-0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

477-481

Subventions

Organisme : Wilhelm Sander-Stiftung
ID : 2016.041.3
Organisme : Wilhelm Sander-Stiftung
ID : 2016.041.2
Organisme : Wilhelm Sander-Stiftung
ID : 2016.041.1

Informations de copyright

© 2023 The Authors. Histopathology published by John Wiley & Sons Ltd.

Références

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Nettersheim D, Jostes S, Sharma R et al. BMP inhibition in seminomas initiates acquisition of pluripotency via NODAL signaling resulting in reprogramming to an embryonal carcinoma. PLoS Genet 2015; 11; e1005415.
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Auteurs

Felix Bremmer (F)

Institute of Pathology, University Medical Center Goettingen, Goettingen, Germany.

Lena Lubk (L)

Institute of Pathology, University Medical Center Goettingen, Goettingen, Germany.

Philipp Ströbel (P)

Institute of Pathology, University Medical Center Goettingen, Goettingen, Germany.

Daniel Nettersheim (D)

Department of Urology, Urological Research Laboratory, Translational UroOncology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.

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