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Hedgehog signaling in the murine melanoma microenvironment.

Hedgehog signaling in the murine melanoma microenvironment. Research Abstract Details 

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  • Hedgehog signaling in the murine melanoma microenvironment. Abstract Text:

    ling gengLing Geng,kyle c cuneoKyle C Cuneo,michael k cooperMichael K Cooper,hong wangHong Wang,konjeti sekharKonjeti Sekhar,allie fuAllie Fu,dennis e hallahanDennis E Hallahan,ling gengLing Geng,kyle c cuneoKyle C Cuneo,michael k cooperMichael K Cooper,hong wangHong Wang,konjeti sekharKonjeti Sekhar,allie fuAllie Fu,dennis e hallahanDennis E Hallahan,ling gengLing Geng,kyle c cuneoKyle C Cuneo,michael k cooperMichael K Cooper,hong wangHong Wang,konjeti sekharKonjeti Sekhar,allie fuAllie Fu,dennis e hallahanDennis E Hallahan,

    The Hedgehog intercellular signaling pathway regulates cell proliferation and differentiation. This pathway has been implicated to play a role in the pathogenesis of cancer and in embryonic blood vessel development. In the current study, Hedgehog signaling in tumor related vasculature and microenvironment was examined using human umbilical vein endothelial cells and B16F0 (murine melanoma) tumors models. Use of exogenous Sonic hedgehog (Shh) peptide significantly increased BrdU incorporation in endothelial cells in vitro by a factor of 2 (P < 0.001). The Hedgehog pathway antagonist cyclopamine effectively reduced Shh-induced proliferation to control levels. To study Hedgehog signaling in vivo a hind limb tumor model with the B16F0 cell line was used. Treatment with 25 mg/kg cyclopamine significantly attenuated BrdU incorporation in tumor cells threefold (P < 0.001), in tumor related endothelial cells threefold (P = 0.004), and delayed tumor growth by 4 days. Immunohistochemistry revealed that the Hedgehog receptor Patched was localized to the tumor stroma and that B16F0 cells expressed Shh peptide. Furthermore, mouse embryonic fibroblasts required the presence of B16F0 cells to express Patched in a co-culture assay system. These studies indicate that Shh peptide produced by melanoma cells induces Patched expression in fibroblasts. To study tumor related angiogenesis a vascular window model was used to monitor tumor vascularity. Treatment with cyclopamine significantly attenuated vascular formation by a factor of 2.5 (P < 0.001) and altered vascular morphology. Furthermore, cyclopamine reduced tumor blood vessel permeability to FITC labeled dextran while having no effect on normal blood vessels. These studies suggest that Hedgehog signaling regulates melanoma related vascular formation and function.

    Hedgehog signaling in the murine melanoma microenvironment. Publishing Authors By Initials

    l gengL Geng,kc cuneoKC Cuneo,mk cooperMK Cooper,h wangH Wang,k sekharK Sekhar,a fuA Fu,de hallahanDE Hallahan,l gengL Geng,kc cuneoKC Cuneo,mk cooperMK Cooper,h wangH Wang,k sekharK Sekhar,a fuA Fu,de hallahanDE Hallahan,l gengL Geng,kc cuneoKC Cuneo,mk cooperMK Cooper,h wangH Wang,k sekharK Sekhar,a fuA Fu,de hallahanDE Hallahan,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

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    Hedgehog signaling in the murine melanoma microenvironment. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Angiogenesis

    VOLUME: 10

    Page Numbers: 259-67

    Journal Abbreviation: Angiogenesis

    ISSN: 0969-6970

    DAY: 31

    MONTH: 08

    YEAR: 2007

    Hedgehog signaling in the murine melanoma microenvironment. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9814575

    Hedgehog signaling in the murine melanoma microenvironment. Keywords Mesh Terms:

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    Grant and Affiliation Information for Hedgehog signaling in the murine melanoma microenvironment.

    AFFILIATION: Department of Radiation Oncology, Vanderbilt University School of Medicine, Nashville, USA, kyle.cuneo@vanderbilt.edu.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: Angiogenesis

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