Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

The chromatin guardian ATRX is a strong prognostic biomarker in melanoma

Title: The chromatin guardian ATRX is a strong prognostic biomarker in melanoma
Authors: Frei, Céline Arlette; Litchfield, Cassandra; Mihic, Alanna; Prutek, Fabiola; Fitsche, André; Wiesmann, Fabius; Wanner, Miriam; Sobottka, Bettina; Mihic-Probst, Daniela; Zuend, Gregor; Zoche, Martin; Zimmermann, Marc; Ziegler, Johanna; Yu, Shuqing; Wollscheid, Bernd; Wildschut, Mattheus H.E.; Wicki, Andreas; Wey, Norbert; Wendt, Fabian; Weller, Michael; Wegmann, Rebekka; Weber, Walter P.; Weber, Sandra; Vlajnic, Tatjana; Vetter, Marcus; Van Drogen, Audrey; Tusup, Marina; Tuncel, Mustafa A.; Toussaint, Nora C.; Tosevski, Vinko; Tolnay, Markus; Thomas, Tinu M.; Theocharides, Alexandre P.A.; Tanna, Tanmay; Stekhoven, Daniel J.; Stark, Stefan; Sreedharan, Vipin T.; Snijder, Berend; Sivapatham, Sujana; Singer, Franziska; Shao, Wenguang; Senti, Gabriela; Schär, Tobias; Schwan, Severin; Schwalie, Petra C.; Schlenker, Ramona; del Castillo, Jacobo Sarabia; Santacroce, Natascha; Rätsch, Gunnar; Rosano-González, María L.; Rommel, Christian; Ritter, Mathilde; Rimmer, Natalie; Prélot, Laurie; Prummer, Michael; Piscuoglio, Salvatore; Pelkmans, Lucas; Pedrioli, Patrick G.A.; Lopéz, Monica Nunez; Nowak, Marta; Nicolet, Stefan; Ng, Charlotte K.Y.; Murri, Riccardo; Muenst, Simone; Moch, Holger; Milani, Emanuela S.; Miglino, Nicola; Metzler, Julian M.; Mena, Julien; Mehnert, Martin; Markolin, Philipp; Manz, Markus G.; Maass, Gerd; Lugert, Sebastian; Lombardo, Flavio C.; Lischetti, Ulrike; Levesque, Mitchell; Lehmann, Kjong Van; Kurzeder, Christian; Kunze, Christian P.; Kuipers, Jack; Kuebler, Werner; Koelzer, Viktor H.; Kahraman, Abdullah; Kahles, André; Jermann, Philip M.; James, Alva R.; Jaeger, Tim M.; Jacobs, Andrea; Jacob, Francis; Irmisch, Anja; Immer, Alexander; Huesser, Tamara; Holtackers, Rene; Herter, Sylvia; Heinzelmann-Schwarz, Viola; Haeuptle, Pirmin; Günther, Detlef; Gut, Gabriele; Grob, Linda; Goetze, Sandra; Frey, Bruno; Frei, Anja L.; Ficek-Pascual, Joanna; Ferreira, Pedro F.; Fedier, André; Esposito, Cinzia; Eschbach, Katja; Erkens, Martin; Engler, Stefanie; Dummer, Reinhard; Davidson, Natalie R.; Danenberg, Esther; D’Costa, Maya; Coelho, Ricardo; Chicherova, Natalia; Chevrier, Stéphane; Casanova, Ruben; Calgua, Byron; Bosshard, Lars; Bonilla, Ximena; Bodenmiller, Bernd; Bertolini, Anne; Bernasconi, Lara; Beisel, Christian; Beerenwinkel, Niko; Beck-Schimmer, Beatrice; Baumhoer, Daniel; Baciu-Drăgan, Monica Andreea; Bacac, Marina; Attinger, Per Olof; Andani, Sonali; Alborelli, Ilaria; Albinus, Jonas; Albert, Silvana I.; Al-Quaddoomi, Faisal S.; Ak, Melike; Aebersold, Rudolf
Contributors: Tumor Profiler Consortium
Publication Year: 2026
Collection: Ecole Polytechnique Fédérale Lausanne (EPFL): Infoscience
Subject Terms: ATRX; Epigenomics; Hypoxia; Melanoma; Tumor progression
Description: In our study, we investigated the role of the chromatin remodeler ATRX in the progression of cutaneous melanoma. We analyzed ATRX protein expression in over 350 melanomas, correlating findings with clinical data, tumor proliferation rates, and vessel density. Additionally, we examined whole-genome sequencing data from 70 melanoma metastases to assess ATRX genetic alterations and compared these with protein expression patterns. We observed a significant reduction in ATRX protein expression in metastases compared to primary tumors: 51% of primary melanomas showed ATRX positivity in over 50% of tumor cells, versus only 25% of metastases (p = 0.01). ATRX loss was associated with earlier metastasis (median 17 vs. 46 months), reduced overall survival (median 69 vs. 162.5 months), and worse tumor-specific survival (p = 0.01). ATRX expression correlated positively with vessel density (rs = 0.3) and negatively with proliferation (rs = – 0.3), suggesting a role in hypoxia response. Genetically, intronic mutations were most frequent (80%), followed by copy number variations (loss: 29%, gain: 37%). Interestingly, ATRX copy number changes did not correlate with protein levels, pointing to epigenetic regulation. Our findings highlight ATRX loss as an early and prognostically relevant event in melanoma, with potential as a therapeutic target. ; SDSC-GE
Document Type: article in journal/newspaper
Language: English
ISSN: 2045-2322
Relation: Scientific reports; https://infoscience.epfl.ch/handle/20.500.14299/258545
DOI: 10.1038/s41598-025-30842-4
Availability: https://doi.org/10.1038/s41598-025-30842-4; https://infoscience.epfl.ch/handle/20.500.14299/258545; https://hdl.handle.net/20.500.14299/258545
Rights: true
Accession Number: edsbas.42CBA928
Database: BASE