Anti-chondrosarcoma effects of PEDF mediated via molecules important to apoptosis, cell cycling, adhesion and invasion
dc.contributor.author | Tan, M. | |
dc.contributor.author | Choong, P. | |
dc.contributor.author | Dass, Crispin | |
dc.date.accessioned | 2017-01-30T11:46:11Z | |
dc.date.available | 2017-01-30T11:46:11Z | |
dc.date.created | 2014-09-02T20:01:14Z | |
dc.date.issued | 2010 | |
dc.identifier.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. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/14830 | |
dc.identifier.doi | 10.1016/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.publisher | Academic Press | |
dc.title | Anti-chondrosarcoma effects of PEDF mediated via molecules important to apoptosis, cell cycling, adhesion and invasion | |
dc.type | Journal Article | |
dcterms.source.volume | 398 | |
dcterms.source.startPage | 613 | |
dcterms.source.endPage | 618 | |
dcterms.source.issn | 0006-291X | |
dcterms.source.title | Biochemical and Biophysical Research Communications | |
curtin.accessStatus | Fulltext not available |