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Int J Mol Sci ; 19(3)2018 Mar 05.
Article in English | MEDLINE | ID: mdl-29510576

ABSTRACT

Lung metastasis constitutes the leading cause of the death in patients with osteosarcoma. We have previously reported that plasminogen activator inhibitor-1 (PAI-1) regulates the invasion and lung metastasis of osteosarcoma cells in a mouse model and as well as in clinical samples. In the present study, we examined the anti-metastatic effect of SK-216, a small compound PAI-1 inhibitor, in human 143B osteosarcoma cells. An in vitro study showed that SK-216 treatment suppressed invasion activity by inhibiting PAI-1 expression in 143B cells, but had no influence on their proliferation or migration. 143B cells treated with SK-216 exhibited reduced matrix metalloproteinase-13 (MMP-13) secretion in a dose-dependent manner. Moreover, intraperitoneal injection of SK-216 into mouse models resulted in downregulation of PAI-1 expression levels in the primary tumors and showed suppression of lung metastases without influencing the proliferative activity of the tumor cells in the primary lesions. These results indicate that SK-216, a PAI-1 inhibitor, may serve as a novel drug to prevent lung metastasis in human osteosarcoma.


Subject(s)
Antineoplastic Agents/therapeutic use , Benzoxazoles/therapeutic use , Dicarboxylic Acids/therapeutic use , Lung Neoplasms/drug therapy , Osteosarcoma/drug therapy , Animals , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/pharmacology , Benzoxazoles/administration & dosage , Benzoxazoles/pharmacology , Cell Line, Tumor , Dicarboxylic Acids/administration & dosage , Dicarboxylic Acids/pharmacology , Lung Neoplasms/secondary , Male , Matrix Metalloproteinase 13/metabolism , Mice , Mice, Nude , Osteosarcoma/pathology , Plasminogen Activator Inhibitor 1/metabolism
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