J
Johanna Liebl
Researcher at Ludwig Maximilian University of Munich
Publications - 31
Citations - 992
Johanna Liebl is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Angiogenesis & Endothelial stem cell. The author has an hindex of 21, co-authored 31 publications receiving 877 citations.
Papers
More filters
Journal ArticleDOI
The V-ATPase-inhibitor Archazolid abrogates tumor metastasis via inhibition of endocytic activation of the Rho-GTPase Rac1
Romina M. Wiedmann,Karin von Schwarzenberg,Andrea Palamidessi,Laura Schreiner,Rebekka Kubisch,Johanna Liebl,Christina Schempp,Dirk Trauner,György Vereb,Stefan Zahler,Ernst Wagner,Rolf Müller,Giorgio Scita,Angelika M. Vollmar +13 more
TL;DR: The results indicate that archazolid effectively decreases metastatic dissemination of breast tumors by impairing the trafficking and spatially restricted activation of EGFR and Rho-GTPase Rac1, which are pivotal for directed movement of cells.
Journal ArticleDOI
Cyclin-dependent Kinase 5 Regulates Endothelial Cell Migration and Angiogenesis
Johanna Liebl,Sabine B. Weitensteiner,György Vereb,Lili Takács,Robert Fürst,Angelika M. Vollmar,Stefan Zahler +6 more
TL;DR: It is shown that cyclin-dependent kinase 5 (Cdk5), an important modulator of neuronal processes, regulates endothelial cell migration and angiogenesis, suggesting Cdk5 as a novel target for antiangiogenic therapy.
Journal ArticleDOI
Targeting cyclin dependent kinase 5 in hepatocellular carcinoma – A novel therapeutic approach
Sandra M. Ehrlich,Johanna Liebl,Maximilian A. Ardelt,Thorsten Lehr,Enrico N. De Toni,Doris Mayr,Lydia Brandl,Thomas Kirchner,Stefan Zahler,Alexander L. Gerbes,Angelika M. Vollmar +10 more
TL;DR: Cdk5 is introduced as a novel drugable target for HCC treatment and the combination of Cdk5 inhibition and DNA damaging agents as a Novel therapeutic approach is suggested.
Journal ArticleDOI
Vacuolar-ATPase inhibition blocks iron metabolism to mediate therapeutic effects in breast cancer
Lina S. Schneider,Karin von Schwarzenberg,Thorsten Lehr,Melanie Ulrich,Rebekka Kubisch-Dohmen,Johanna Liebl,Dirk Trauner,Dirk Menche,Angelika M. Vollmar +8 more
TL;DR: This study offers preclinical evidence of an important metabolic mechanism underlying the antitumor activity of inhibitors of the vacuolar-type ATPase (V-ATPase), a heteromultimeric proton pump, and links V- ATPase to cell-cycle progression and DNA synthesis in cancer cells.
Journal ArticleDOI
Twice switched at birth: cell cycle-independent roles of the "neuron-specific" cyclin-dependent kinase 5 (Cdk5) in non-neuronal cells.
TL;DR: Issues of pharmacological inhibition, the versatile roles, and the growing evidence for the functional importance of Cdk5 in non-neuronal tissues are discussed, including blood cells, tumor cells, epithelial cells, the vascular endothelium, testis, adipose and endocrine tissues.