Chondrosarcoma and Peroxisome Proliferator-Activated Receptor

被引:16
|
作者
Nishida, K. [1 ,2 ]
Kunisada, T. [2 ]
Shen, Z. N. [2 ]
Kadota, Y. [2 ]
Hashizume, K. [2 ]
Ozaki, T. [2 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Human Morphol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Orthopaed Surg, Okayama 7008558, Japan
关键词
D O I
10.1155/2008/250568
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Induction of differentiation and apoptosis in cancer cells by ligands of PPAR gamma is a novel therapeutic approach to malignant tumors. Chondrosarcoma (malignant cartilage tumor) and OUMS-27 cells (cell line established from grade III human chondrosarcoma) express PPAR gamma. PPAR gamma ligands inhibited cell proliferation in a dose-dependent manner, and induced apoptosis of OUMS-27. The higher-grade chondrosarcoma expressed a higher amount of antiapoptotic Bcl-xL in vivo. The treatment of OUMS-27 by 15d-PGJ(2), the most potent endogenous ligand for PPAR gamma, downregulated expression of Bcl-xL and induced transient upregulation of proapoptotic Bax, which could accelerate cytochrome c release from mitochondria to the cytosol, followed by induction of caspase-dependent apoptosis. 15d-PGJ(2) induced the expression of CDK inhibitor p21 protein in human chondrosarcoma cells, which appears to be involved in the mechanism of inhibition of cell proliferation. These findings suggest that targeted therapy with PPAR gamma ligands could be a novel strategy against chondrosarcoma. Copyright (C) 2008 K. Nishida et al.
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页数:7
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