W
Walter Berger
Researcher at Medical University of Vienna
Publications - 396
Citations - 16667
Walter Berger is an academic researcher from Medical University of Vienna. The author has contributed to research in topics: Cancer & Cell culture. The author has an hindex of 63, co-authored 359 publications receiving 14045 citations. Previous affiliations of Walter Berger include University of Vienna & Université libre de Bruxelles.
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Human tripartite motif protein 52 is required for cell context-dependent proliferation.
Stefan Benke,Benedikt Agerer,Lisa Haas,Martin Stöger,Alexander Lercher,Lisa Gabler,Izabella Kiss,Sara Scinicariello,Walter Berger,Andreas Bergthaler,Anna C. Obenauf,Gijs A. Versteeg +11 more
TL;DR: It is reported here that TRIM52 ablation significantly diminished the proliferation of specific glioblastoma cell lines in cell culture and mouse xenografts by compromising their cell cycle progression in a p53-dependent manner.
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Effects of Multidrug Resistance-Related ATP-Binding-Cassette Transporter Proteins on the Cytoskeletal Activity of Cytochalasins
TL;DR: It is shown that both the microfilament-disrupting and the cytotoxic activity of cytochalasins are reduced in parallel with increased P-gp expression and restorable by P-GP-modulating agents, and the polykaryon-inducing activity of Cytochalasin D is suggested as a specific indicator for a P- gp-mediated multidrug-resistance phenotype and the reversing potency of chemosensitizers.
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Nanoformulations of anticancer thiosemicarbazones to reduce methemoglobin formation and improve anticancer activity
Britta Fischer,Kushtrim Kryeziu,Sebastian Kallus,Petra Heffeter,Walter Berger,Christian R. Kowol,Christian R. Kowol,Bernhard K. Keppler,Bernhard K. Keppler +8 more
TL;DR: In this article, the authors encapsulated Triapine into polymeric nanoparticles and remote-loaded liposomes to improve the drug pharmacokinetics as well as targeted delivery, but burst release of triapine from both nano-formulations was observed, making the synthesis of two novel triapy derivatives necessary in order to improve remoteloading properties.
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MAP kinase activity supported by BRAF V600E mutation rather than gene amplification is associated with ETV1 expression in melanoma brain metastases
Peter Birner,Anna S. Berghoff,Carina Dinhof,Christine Pirker,David Capper,Sebastian F. Schoppmann,Peter Petzelbauer,Andreas von Deimling,Walter Berger,Matthias Preusser +9 more
TL;DR: ETV1 expression is a rare event in human melanoma and seems to be rather based on hyperactivation of MAPK signals, by BRAFV600E mutation, than on ETV1 gene amplification, Consequently, therapeutic inhibition of BRAF and the downstream MAPK pathway also down-regulates oncogenic ETV 1 expression.
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Synergistic effect of Sorafenib and Sunitinib with Enzastaurin, a selective protein kinase C inhibitor in renal cell carcinoma cell lines
Ursula M. Vogl,Walter Berger,Michael Micksche,Christine Pirker,Wolfgang Lamm,Oskar Pichelmeyer,Christoph C. Zielinski,Manuela Schmidinger +7 more
TL;DR: Both Sorafenib and Sunitinib with Enzastaurin at concentrations feasible in vivo showed a synergistic reduction of viable RCC cells by inhibiting cell growth through inhibition of phospho-S6-kinase and GSK3-beta.