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    Anti-chondrosarcoma effects of PEDF mediated via molecules important to apoptosis, cell cycling, adhesion and invasion

    Access Status
    Fulltext not available
    Authors
    Tan, M.
    Choong, P.
    Dass, Crispin
    Date
    2010
    Type
    Journal Article
    
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    Citation
    Tan, M. and Choong, P. and Dass, C. 2010. Anti-chondrosarcoma effects of PEDF mediated via molecules important to apoptosis, cell cycling, adhesion and invasion. Biochemical and Biophysical Research Communications. 398: pp. 613-618.
    Source Title
    Biochemical and Biophysical Research Communications
    DOI
    10.1016/j.bbrc.2010.05.098
    ISSN
    0006-291X
    URI
    http://hdl.handle.net/20.500.11937/14830
    Collection
    • Curtin Research Publications
    Abstract

    Chondrosarcoma develops as a result of overgrowth of chondrocytes and overproduction of cartilage matrix. It is currently surgically treated, although non-invasive methods are being sought. In this report, pigment epithelium-derived factor (PEDF) induced apoptosis in the chondrosarcoma cell line - JJ012, with upregulation of Bax, Fas, caspase-3 and -6 and downregulation of Bcl-2. Cell cycling was also decreased with decreased expression of p38, p-Akt, p-Erk and JNK1 and increased expression of p73 and E2F1. Furthermore, PEDF increased adhesion of cells to collagen-I, with decreased expression of p-Fak, RhoA and cdc42. Invasion of cells through collagen-I was also reduced by PEDF, with decreased expression of uPAR, MMP-14 and increased expression of PAI-1. These findings seminally indicate that PEDF may have potential as an anti-cancer agent against chondrosarcoma.

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