M
Matthias Artaker
Researcher at Medical University of Vienna
Publications - 8
Citations - 559
Matthias Artaker is an academic researcher from Medical University of Vienna. The author has contributed to research in topics: HDAC1 & Stromal cell. The author has an hindex of 7, co-authored 8 publications receiving 468 citations.
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Journal ArticleDOI
PDGFR blockade is a rational and effective therapy for NPM-ALK–driven lymphomas
Daniela Laimer,Helmut Dolznig,Karoline Kollmann,Paul Vesely,Paul Vesely,Michaela Schlederer,Olaf Merkel,Olaf Merkel,Ana Iris Schiefer,Melanie R. Hassler,Susi Heider,Lena Amenitsch,Christiane Thallinger,Philipp B. Staber,Philipp B. Staber,Ingrid Simonitsch-Klupp,Matthias Artaker,Sabine Lagger,Sabine Lagger,Suzanne D. Turner,Stefano Pileri,Pier Paolo Piccaluga,Peter Valent,Katia Messana,Indira Landra,Thomas Weichhart,Sylvia Knapp,Sylvia Knapp,Medhat Shehata,Maria Todaro,Veronika Sexl,Gerald Höfler,Roberto Piva,Roberto Piva,Enzo Medico,Bruce Ruggeri,Mangeng Cheng,Robert Eferl,Gerda Egger,Josef M. Penninger,Ulrich Jaeger,Richard Moriggl,Giorgio Inghirami,Lukas Kenner +43 more
TL;DR: It is shown that the activator protein 1 family members JUN and JUNB promote lymphoma development and tumor dissemination through transcriptional regulation of platelet-derived growth factor receptor-β (PDGFRB) in a mouse model of NPM-ALK–triggered lymphomagenesis.
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IGFBP7, a novel tumor stroma marker, with growth-promoting effects in colon cancer through a paracrine tumor–stroma interaction
Christian Rupp,Martin Scherzer,Albin Rudisch,Christine Unger,Christian Haslinger,Norbert Schweifer,Matthias Artaker,Harini Nivarthi,Richard Moriggl,Markus Hengstschläger,Dontscho Kerjaschki,Wolfgang Sommergruber,Helmut Dolznig,P Garin-Chesa +13 more
TL;DR: It is shown that in contrast to its tumor-suppressor function in epithelial cells, IGFPB7 can promote anchorage-independent growth in malignant mesenchymal cells and in epitheric cells with an EMT phenotype and can induce colony formation in colon cancer cells co-cultured with IGFBP7-expressing CAFs by a paracrine tumor–stroma interaction.
Journal ArticleDOI
Autocrine WNT2 signaling in fibroblasts promotes colorectal cancer progression
Nina Kramer,J Schmöllerl,Christine Unger,Harini Nivarthi,Albin Rudisch,Daniela Unterleuthner,Martin Scherzer,Angelika Riedl,Matthias Artaker,Ilija Crncec,D Lenhardt,Thomas Schwarz,B Prieler,Xiaonan Han,Markus Hengstschläger,Julia Schüler,Robert Eferl,Richard Moriggl,Wolfgang Sommergruber,Helmut Dolznig +19 more
TL;DR: It is shown for the first time that WNT2 is one of the most significantly induced genes in CRC stroma as compared to normal stroma, and W NT2 and its receptor are classifies as promising stromal targets to confine cancer progression in combination with conventional or targeted therapies.
Journal ArticleDOI
Stat5 regulates cellular iron uptake of erythroid cells via IRP-2 and TfR-1.
Marc A. Kerenyi,Florian Grebien,Helmuth Gehart,Manfred Schifrer,Matthias Artaker,Boris Kovacic,Hartmut Beug,Richard Moriggl,Ernst W. Müllner +8 more
TL;DR: It is demonstrated that mice completely lacking Stat5 suffer from microcytic anemia due to reduced expression of the antiapoptotic proteins Bcl-x(L) and Mcl-1 followed by enhanced apoptosis, establishing an unexpected mechanistic link between EpoR/Jak/Stat signaling and iron metabolism, processes absolutely essential for erythropoiesis and life.
Journal ArticleDOI
A single allele of Hdac2 but not Hdac1 is sufficient for normal mouse brain development in the absence of its paralog
Astrid Hagelkruys,Sabine Lagger,Julia Krahmer,Alexandra Leopoldi,Matthias Artaker,Oliver Pusch,Jürgen Zezula,Simon Weissmann,Yunli Xie,Christian Schöfer,Michaela Schlederer,Gerald Brosch,Patrick Matthias,Jim Selfridge,Hans Lassmann,Jürgen A. Knoblich,Christian Seiser +16 more
TL;DR: The data indicate that HDAC1 and HDAC2 have a common function in maintaining proper chromatin structures and show that Hdac2 has a unique role by controlling the fate of neural progenitors during normal brain development.