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    Vascular endothelial growth factor and not cyclooxygenase 2 promotes endothelial cell viability in the pancreatic tumor microenvironment.

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    Authors
    Toomey, Desmond P
    Manahan, Ellen
    McKeown, Ciara
    Rogers, Annamarie
    McMillan, Helen
    Geary, Michael
    Conlon, Kevin C
    Murphy, Joseph F
    Affiliation
    Professorial Surgical Unit, University of Dublin, Trinity College, Dublin, Ireland.
    Issue Date
    2010-07
    MeSH
    Angiogenesis Inhibitors
    Anti-Inflammatory Agents, Non-Steroidal
    Cell Survival
    Cyclooxygenase 2
    Cyclooxygenase 2 Inhibitors
    Dinoprostone
    Endothelium, Vascular
    Humans
    Neovascularization, Pathologic
    Pancreatic Neoplasms
    Pyrazoles
    Sulfonamides
    Tumor Cells, Cultured
    Vascular Endothelial Growth Factors
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    Citation
    Vascular endothelial growth factor and not cyclooxygenase 2 promotes endothelial cell viability in the pancreatic tumor microenvironment. 2010, 39 (5):595-603 Pancreas
    Publisher
    Pancreas
    Journal
    Pancreas
    URI
    http://hdl.handle.net/10147/251857
    DOI
    10.1097/MPA.0b013e3181c6575d
    PubMed ID
    20118820
    Abstract
    Cyclooxygenase 2 (COX-2) and vascular endothelial growth factor (VEGF), often coexpressed in cancer, are associated with poor prognosis. However, results from pancreatic cancer trials of their inhibitors were disappointing. This study delineated the role of COX-2 and nonsteroidal anti-inflammatory drugs in angiogenesis and VEGF regulation.
    Item Type
    Article
    Language
    en
    ISSN
    1536-4828
    ae974a485f413a2113503eed53cd6c53
    10.1097/MPA.0b013e3181c6575d
    Scopus Count
    Collections
    Tallaght University Hospital

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