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    Development of a modified hollow fibre assay for studying agents targeting the tumour neovasculature.

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    Publication date
    2009-07-13T09:17:14Z
    Author
    Shnyder, Steven D.
    Jubb, E.
    Hasan, J.
    Cooper, Patricia A.
    Bibby, Michael C.
    Jayson, G.C.
    Pilarinou, E.
    Keyword
    Hollow fibre assay
    Anti-vascular effects
    Angiogenesis
    H460 non-small cell lung carcinoma cell line
    VEGF
    Peer-Reviewed
    Yes
    
    Metadata
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    Abstract
    Background: Previous studies have shown extensive vascularisation surrounding subcutaneously implanted fibres when the duration of the US National Cancer Institute (NCI) hollow fibre assay was prolonged. Materials and Methods: The feasibility of adapting the NCI assay for evaluating agents targeting the tumour vasculature was investigated in vitro and in vivo. Finally, in the optimised assay, changes in neovasculature formation around the fibres following treatment with the anti-vascular agent paclitaxel were quantified by immunohistochemistry. Results: Correlations between cell number seeded, time in culture and vascular endothelial growth factor (VEGF) secretion were seen. In vivo studies showed that transplanting single rather than 3 fibres at a site reduced inflammation, reducing the length of the fibre transplanted, as did without any significant loss in cell growth over 21 days. A statistically significant reduction in neovascularisation surrounding the fibres was seen accompanying paclitaxel treatment. Conclusion: Modifications made here to the NCI hollow fibre assay demonstrate its potential for analysing anti-tumour vasculature agents.
    URI
    http://hdl.handle.net/10454/2975
    Version
    No full-text available in the repository
    Citation
    Shnyder, S.D., Hasan, J., Jubb, E., Cooper, P.A. and Bibby, M.C. et al. (2005) Development of a modified hollow fibre assay for studying agents targeting the tumour neovasculature. Anticancer Research. Vol. 25, No. 3B, pp. 1889-1894.
    Link to publisher’s version
    http://ar.iiarjournals.org/content/25/3B/1889.abstract
    Type
    Article
    Collections
    Life Sciences Publications

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