Chondrosarcoma and Peroxisome Proliferator-Activated Receptor
被引:16
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Nishida, K.
[1
,2
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Kunisada, T.
[2
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Shen, Z. N.
[2
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Kadota, Y.
[2
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Hashizume, K.
论文数: 0引用数: 0
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Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Orthopaed Surg, Okayama 7008558, JapanOkayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Human Morphol, Okayama 7008558, Japan
Hashizume, K.
[2
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Ozaki, T.
论文数: 0引用数: 0
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Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Orthopaed Surg, Okayama 7008558, JapanOkayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Human Morphol, Okayama 7008558, Japan
Ozaki, T.
[2
]
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[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
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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Univ Calif Los Angeles, Div Hematol & Oncol, Cedars Sinai Med Ctr, Sch Med, Los Angeles, CA 90048 USAUniv Calif Los Angeles, Div Hematol & Oncol, Cedars Sinai Med Ctr, Sch Med, Los Angeles, CA 90048 USA
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Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USAUniv Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 1492, Houston, TX 77030 USA
Wang, D.
Ning, W.
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Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USAUniv Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 1492, Houston, TX 77030 USA
Ning, W.
Xie, D.
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Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USAUniv Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 1492, Houston, TX 77030 USA
Xie, D.
Guo, L.
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Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USAUniv Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 1492, Houston, TX 77030 USA
Guo, L.
DuBois, R. N.
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Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 1492, Houston, TX 77030 USA
Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USAUniv Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 1492, Houston, TX 77030 USA