Involvement of matrix metalloproteinase-3 in CCL5/CCR5 pathway of chondrosarcomas metastasis
| Autor: | Tzu-Wei Tan, Yuh-Tzy Lin, Chih-Hsin Tang, Ayaho Yamamoto, Yi-Chin Fong |
|---|---|
| Rok vydání: | 2010 |
| Předmět: |
Small interfering RNA
Blotting Western Chondrosarcoma Enzyme-Linked Immunosorbent Assay Biology Matrix metalloproteinase Polymerase Chain Reaction Biochemistry CCL5 stomatognathic system Cell Line Tumor parasitic diseases medicine Humans Neoplasm Metastasis RNA Small Interfering Chemokine CCL5 Protein kinase B PI3K/AKT/mTOR pathway Pharmacology virus diseases hemic and immune systems Cell migration medicine.disease Immunohistochemistry stomatognathic diseases Cell culture Cancer research Matrix Metalloproteinase 3 |
| Zdroj: | Biochemical Pharmacology. 79:209-217 |
| ISSN: | 0006-2952 |
| DOI: | 10.1016/j.bcp.2009.08.006 |
| Popis: | CCL5 (previously called RANTES) was originally recognized as a product of activated T cells, and plays a crucial role in the migration and metastasis of human cancer cells. It has been reported that the effect of CCL5 is mediated via CCR receptors. We found that human chondrosarcoma tissues had significant expression of the CCL5 and CCR5, which was higher than that in normal cartilage. We also found CCL5 increased the migration and matrix metalloproteinases-3 (MMP)-3 expression in human chondrosarcoma cells (JJ012 cells). In addition, MMP-3 small interfering RNA and inhibitor inhibited the CCL5-induced cell migration. Activations of phosphatidylinositol 3-kinase (PI3K), Akt and NF-kappaB pathways after CCL5 treatment was demonstrated, and CCL5-induced expression of MMP-3 and migration activity was inhibited by the specific inhibitor of PI3K, Akt and NF-kappaB cascades. Taken together, these results indicate that CCL5 and CCR5 interaction enhanced migration of chondrosarcoma cells through the increase of MMP-3 production. |
| Databáze: | OpenAIRE |
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