Dokument: Molecular and epigenetic ex vivo profiling of testis cancer-associated fibroblasts and their interaction with germ cell tumor cells and macrophages

Titel:Molecular and epigenetic ex vivo profiling of testis cancer-associated fibroblasts and their interaction with germ cell tumor cells and macrophages
URL für Lesezeichen:https://docserv.uni-duesseldorf.de/servlets/DocumentServlet?id=67629
URN (NBN):urn:nbn:de:hbz:061-20241121-115712-5
Kollektion:Publikationen
Sprache:Englisch
Dokumententyp:Wissenschaftliche Texte » Artikel, Aufsatz
Medientyp:Text
Autoren: Stephan, Alexa [Autor]
Suhrmann, Jan-Henrik [Autor]
Skowron, Margaretha A. [Autor]
Che, Yue [Autor]
Poschmann, Gereon [Autor]
Petzsch, Patrick [Autor]
Kresbach,Catena [Autor]
Wruck, Wasco [Autor]
Pongratanakul, Pailin [Autor]
Adjaye, James [Autor]
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Dateien vom 21.11.2024 / geändert 21.11.2024
Stichwörter:Cancer-associated fibroblasts, Microenvironment, Germ cell tumors, DNA methylation, Fibroblasts, Secretome, Extracellular matrix
Beschreibung:Germ cell tumors (GCT) are the most common solid tumors in young men of age 15 - 40. In previous studies, we profiled the interaction of GCT cells with cells of the tumor microenvironment (TM), which showed that especially the 3D interaction of fibroblasts (FB) or macrophages with GCT cells influenced the growth behavior and cisplatin response as well as the transcriptome and secretome of the tumor cells, suggesting that the crosstalk of these cells with GCT cells is crucial for tumor progression and therapy outcome.
In this study, we shed light on the mechanisms of activation of cancer-associated fibroblasts (CAF) in the GCT setting and their effects on GCT cells lines and the monocyte cell line THP-1. Ex vivo cultures of GCT-derived CAF were established and characterized molecularly and epigenetically by performing DNA methylation arrays, RNA sequencing, and mass spectrometry-based secretome analysis.
We demonstrated that the activation state of CAF is influenced by their former prevailing tumor environment in which they have resided. Hereby, we postulate that seminoma (SE) and embryonal carcinoma (EC) activate CAF, while teratoma (TER) play only a minor role in CAF formation. In turn, CAF influence proliferation and the expression of cisplatin sensitivity-related factors in GCT cells lines as well as polarization of in vitro-induced macrophages by the identified effector molecules IGFBP1, LGALS3BP, LYVE1, and PTX3.
Our data suggests that the vital interaction of CAF with GCT cells and with macrophages has a huge influence on shaping the extracellular matrix as well as on recruitment of immune cells to the TM. In conclusion, therapeutically interfering with CAF and / or macrophages in addition to the standard therapy might slow-down progression of GCT and re-shaping of the TM to a tumor-promoting environment.
Significance: The interaction of CAF with GCT and macrophages considerably influences the microenvironment. Thus, therapeutically interfering with CAF might slow-down progression of GCT and re-shaping of the microenvironment to a tumor-promoting environment.
Rechtliche Vermerke:Originalveröffentlichung:
Stephan, A., Suhrmann, J.-H., Skowron, M. A., Che, Y., Poschmann, G., Petzsch, P., Kresbach, C., Wruck, W., Pongratanakul, P., Adjaye, J., Stühler, K., Köhrer, K., Schüller, U., & Nettersheim, D. (2024). Molecular and epigenetic ex vivo profiling of testis cancer-associated fibroblasts and their interaction with germ cell tumor cells and macrophages. Matrix Biology, 132, 10–23. https://doi.org/10.1016/j.matbio.2024.06.001
Lizenz:Creative Commons Lizenzvertrag
Dieses Werk ist lizenziert unter einer Creative Commons Namensnennung 4.0 International Lizenz
Fachbereich / Einrichtung:Medizinische Fakultät
Dokument erstellt am:21.11.2024
Dateien geändert am:21.11.2024
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