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  1. AU="Bierbaumer, Lisa"
  2. AU="Rashid, Muhammad"
  3. AU="Huang, Chiun-Sheng"
  4. AU="Shevchuk, O O"
  5. AU="Mulvihill, Emily"
  6. AU="Gandhi, Adarsh"
  7. AU="Zhao, Chuanrui"
  8. AU="Shelley Wiart"
  9. AU="Lydia E. Wroblewski" AU="Lydia E. Wroblewski"
  10. AU="Paterson, Ross"
  11. AU="Alexander Marx"
  12. AU="Robinson, Jill"
  13. AU="Mitchell, Adam W M"
  14. AU="Ingham, Jesse R"

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  1. Artikel ; Online: The YAP/TAZ Pathway in Osteogenesis and Bone Sarcoma Pathogenesis.

    Kovar, Heinrich / Bierbaumer, Lisa / Radic-Sarikas, Branka

    Cells

    2020  Band 9, Heft 4

    Abstract: YAP and TAZ are intracellular messengers communicating multiple interacting extracellular biophysical and biochemical cues to the transcription apparatus in the nucleus and back to the cell/tissue microenvironment interface through the regulation of ... ...

    Abstract YAP and TAZ are intracellular messengers communicating multiple interacting extracellular biophysical and biochemical cues to the transcription apparatus in the nucleus and back to the cell/tissue microenvironment interface through the regulation of cytoskeletal and extracellular matrix components. Their activity is negatively and positively controlled by multiple phosphorylation events. Phenotypically, they serve an important role in cellular plasticity and lineage determination during development. As they regulate self-renewal, proliferation, migration, invasion and differentiation of stem cells, perturbed expression of YAP/TAZ signaling components play important roles in tumorigenesis and metastasis. Despite their high structural similarity, YAP and TAZ are functionally not identical and may play distinct cell type and differentiation stage-specific roles mediated by a diversity of downstream effectors and upstream regulatory molecules. However, YAP and TAZ are frequently looked at as functionally redundant and are not sufficiently discriminated in the scientific literature. As the extracellular matrix composition and mechanosignaling are of particular relevance in bone formation during embryogenesis, post-natal bone elongation and bone regeneration, YAP/TAZ are believed to have critical functions in these processes. Depending on the differentiation stage of mesenchymal stem cells during endochondral bone development, YAP and TAZ serve distinct roles, which are also reflected in bone tumors arising from the mesenchymal lineage at different developmental stages. Efforts to clinically translate the wealth of available knowledge of the pathway for cancer diagnostic and therapeutic purposes focus mainly on YAP and TAZ expression and their role as transcriptional co-activators of TEAD transcription factors but rarely consider the expression and activity of pathway modulatory components and other transcriptional partners of YAP and TAZ. As there is a growing body of evidence for YAP and TAZ as potential therapeutic targets in several cancers, we here interrogate the applicability of this concept to bone tumors. To this end, this review aims to summarize our current knowledge of YAP and TAZ in cell plasticity, normal bone development and bone cancer.
    Mesh-Begriff(e) Adaptor Proteins, Signal Transducing/metabolism ; Animals ; Bone Neoplasms/genetics ; Bone Neoplasms/metabolism ; Bone Neoplasms/pathology ; Carcinogenesis/genetics ; Carcinogenesis/metabolism ; Carcinogenesis/pathology ; Humans ; Osteogenesis ; Sarcoma/genetics ; Sarcoma/metabolism ; Sarcoma/pathology ; Signal Transduction ; Trans-Activators/metabolism
    Chemische Substanzen Adaptor Proteins, Signal Transducing ; Trans-Activators
    Sprache Englisch
    Erscheinungsdatum 2020-04-15
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells9040972
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Cell culture models of oral mucosal barriers: A review with a focus on applications, culture conditions and barrier properties.

    Bierbaumer, Lisa / Schwarze, Uwe Yacine / Gruber, Reinhard / Neuhaus, Winfried

    Tissue barriers

    2018  Band 6, Heft 3, Seite(n) 1479568

    Abstract: Understanding the function of oral mucosal epithelial barriers is essential for a plethora of research fields such as tumor biology, inflammation and infection diseases, microbiomics, pharmacology, drug delivery, dental and biomarker research. The ... ...

    Abstract Understanding the function of oral mucosal epithelial barriers is essential for a plethora of research fields such as tumor biology, inflammation and infection diseases, microbiomics, pharmacology, drug delivery, dental and biomarker research. The barrier properties are comprised by a physical, a transport and a metabolic barrier, and all these barrier components play pivotal roles in the communication between saliva and blood. The sum of all epithelia of the oral cavity and salivary glands is defined as the blood-saliva barrier. The functionality of the barrier is regulated by its microenvironment and often altered during diseases. A huge array of cell culture models have been developed to mimic specific parts of the blood-saliva barrier, but no ultimate standard in vitro models have been established. This review provides a comprehensive overview about developed in vitro models of oral mucosal barriers, their applications, various cultivation protocols and corresponding barrier properties.
    Mesh-Begriff(e) Cell Culture Techniques ; Humans ; Mouth Mucosa/physiopathology
    Sprache Englisch
    Erscheinungsdatum 2018-09-25
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ISSN 2168-8370
    ISSN (online) 2168-8370
    DOI 10.1080/21688370.2018.1479568
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: High-content drug screening in zebrafish xenografts reveals high efficacy of dual MCL-1/BCL-X

    Grissenberger, Sarah / Sturtzel, Caterina / Wenninger-Weinzierl, Andrea / Radic-Sarikas, Branka / Scheuringer, Eva / Bierbaumer, Lisa / Etienne, Vesnie / Némati, Fariba / Pascoal, Susana / Tötzl, Marcus / Tomazou, Eleni M / Metzelder, Martin / Putz, Eva M / Decaudin, Didier / Delattre, Olivier / Surdez, Didier / Kovar, Heinrich / Halbritter, Florian / Distel, Martin

    Cancer letters

    2022  Band 554, Seite(n) 216028

    Abstract: Ewing sarcoma is a pediatric bone and soft tissue cancer with an urgent need for new therapies to improve disease outcome. To identify effective drugs, phenotypic drug screening has proven to be a powerful method, but achievable throughput in mouse ... ...

    Abstract Ewing sarcoma is a pediatric bone and soft tissue cancer with an urgent need for new therapies to improve disease outcome. To identify effective drugs, phenotypic drug screening has proven to be a powerful method, but achievable throughput in mouse xenografts, the preclinical Ewing sarcoma standard model, is limited. Here, we explored the use of xenografts in zebrafish for high-throughput drug screening to discover new combination therapies for Ewing sarcoma. We subjected xenografts in zebrafish larvae to high-content imaging and subsequent automated tumor size analysis to screen single agents and compound combinations. We identified three drug combinations effective against Ewing sarcoma cells: Irinotecan combined with either an MCL-1 or an BCL-X
    Mesh-Begriff(e) Humans ; Animals ; Mice ; Sarcoma, Ewing/drug therapy ; Sarcoma, Ewing/genetics ; Sarcoma, Ewing/metabolism ; Zebrafish/metabolism ; Myeloid Cell Leukemia Sequence 1 Protein/genetics ; Myeloid Cell Leukemia Sequence 1 Protein/metabolism ; Drug Evaluation, Preclinical ; Heterografts ; Apoptosis ; bcl-X Protein/genetics ; bcl-X Protein/metabolism ; Cell Line, Tumor
    Chemische Substanzen Myeloid Cell Leukemia Sequence 1 Protein ; bcl-X Protein
    Sprache Englisch
    Erscheinungsdatum 2022-12-01
    Erscheinungsland Ireland
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 195674-7
    ISSN 1872-7980 ; 0304-3835
    ISSN (online) 1872-7980
    ISSN 0304-3835
    DOI 10.1016/j.canlet.2022.216028
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: YAP/TAZ inhibition reduces metastatic potential of Ewing sarcoma cells.

    Bierbaumer, Lisa / Katschnig, Anna M / Radic-Sarikas, Branka / Kauer, Maximilian O / Petro, Jeffrey A / Högler, Sandra / Gurnhofer, Elisabeth / Pedot, Gloria / Schäfer, Beat W / Schwentner, Raphaela / Mühlbacher, Karin / Kromp, Florian / Aryee, Dave N T / Kenner, Lukas / Uren, Aykut / Kovar, Heinrich

    Oncogenesis

    2021  Band 10, Heft 1, Seite(n) 2

    Abstract: Ewing sarcoma (EwS) is a highly metastatic bone cancer characterized by the ETS fusion oncoprotein EWS-FLI1. EwS cells are phenotypically highly plastic and switch between functionally distinct cell states dependent on EWS-FLI1 fluctuations. Whereas EWS- ... ...

    Abstract Ewing sarcoma (EwS) is a highly metastatic bone cancer characterized by the ETS fusion oncoprotein EWS-FLI1. EwS cells are phenotypically highly plastic and switch between functionally distinct cell states dependent on EWS-FLI1 fluctuations. Whereas EWS-FLI1
    Sprache Englisch
    Erscheinungsdatum 2021-01-08
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2674437-5
    ISSN 2157-9024
    ISSN 2157-9024
    DOI 10.1038/s41389-020-00294-8
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel: Dynamics of CRISPR/Cas9-mediated genomic editing of the

    Scharf, Irene / Bierbaumer, Lisa / Huber, Heidemarie / Wittmann, Philipp / Haider, Christine / Pirker, Christine / Berger, Walter / Mikulits, Wolfgang

    Oncology letters

    2017  Band 15, Heft 2, Seite(n) 2441–2450

    Abstract: Genomic editing using the CRISPR/Cas9 technology allows selective interference with gene expression. With this method, a multitude of haploid and diploid cells from different organisms have been employed to successfully generate knockouts of genes coding ...

    Abstract Genomic editing using the CRISPR/Cas9 technology allows selective interference with gene expression. With this method, a multitude of haploid and diploid cells from different organisms have been employed to successfully generate knockouts of genes coding for proteins or small RNAs. Yet, cancer cells exhibiting an aberrant ploidy are considered to be less accessible to CRISPR/Cas9-mediated genomic editing, as amplifications of the targeted gene locus could hamper its effectiveness. Here we examined the suitability of CRISPR/Cas9 to knockout the receptor tyrosine kinase Axl in the human hepatoma cell lines HLF and SNU449. The genomic editing events were validated in two single cell clones each from putative HLF and SNU449 knockout cells (HLF-Axl
    Sprache Englisch
    Erscheinungsdatum 2017-12-13
    Erscheinungsland Greece
    Dokumenttyp Journal Article
    ZDB-ID 2573196-8
    ISSN 1792-1082 ; 1792-1074
    ISSN (online) 1792-1082
    ISSN 1792-1074
    DOI 10.3892/ol.2017.7605
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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