Back to Search Start Over

Loss of XIAP sensitizes colon cancer cells to PPARgamma independent antitumor effects of troglitazone and 15-PGJ2.

Authors :
Qiao L
Dai Y
Gu Q
Chan KW
Ma J
Lan HY
Zou B
Rocken C
Ebert MP
Wong BC
Source :
Cancer letters [Cancer Lett] 2008 Sep 18; Vol. 268 (2), pp. 260-71. Date of Electronic Publication: 2008 May 13.
Publication Year :
2008

Abstract

We investigated whether the anticancer effect of a combination of XIAP down-regulation and PPAR gamma activation on colon cancer is PPARgamma receptor dependent. HCT116-XIAP(+/+) cells and HCT116-XIAP(-/-) cells were treated with troglitazone or 15-deoxy-Delta(12,14)-prostaglandin J2 (15-PGJ2) with or without prior exposure to PPARgamma inhibitor GW9662. Cell proliferation and apoptosis was evaluated. Athymic mice carrying HCT116-XIAP(-/-) cells-derived tumors were treated with troglitazone in the presence or absence of GW9662. Inhibition of cell proliferation and induction of apoptosis by troglitazone and 15-PGJ2 were more prominent in HCT116-XIAP(-/-) cells. PPARgamma ligand-induced growth inhibition, apoptosis, caspase and PARP cleavage could not be blocked by GW9662. Troglitazone significantly retarded growth of xenograft tumors and this effect was not blocked by GW9662. Marked apoptosis and an up-regulation of E-cadherin were observed in xenograft tumor tissues, and GW9662 did not affect these effects. Thus, a combination of XIAP down-regulation and PPARgamma ligands exert a significant anticancer effect in colon cancer via a PPARgamma independent pathway.

Details

Language :
English
ISSN :
1872-7980
Volume :
268
Issue :
2
Database :
MEDLINE
Journal :
Cancer letters
Publication Type :
Academic Journal
Accession number :
18477501
Full Text :
https://doi.org/10.1016/j.canlet.2008.04.003