Show simple item record

dc.contributor.authorTan, M.
dc.contributor.authorChoong, P.
dc.contributor.authorDass, Crispin
dc.date.accessioned2017-01-30T11:46:11Z
dc.date.available2017-01-30T11:46:11Z
dc.date.created2014-09-02T20:01:14Z
dc.date.issued2010
dc.identifier.citationTan, 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.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/14830
dc.identifier.doi10.1016/j.bbrc.2010.05.098
dc.description.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.

dc.publisherAcademic Press
dc.titleAnti-chondrosarcoma effects of PEDF mediated via molecules important to apoptosis, cell cycling, adhesion and invasion
dc.typeJournal Article
dcterms.source.volume398
dcterms.source.startPage613
dcterms.source.endPage618
dcterms.source.issn0006-291X
dcterms.source.titleBiochemical and Biophysical Research Communications
curtin.accessStatusFulltext not available


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record