Metastatin: a hyaluronan-binding complex from cartilage that inhibits tumor growth.

N Liu, R K Lapcevich, C B Underhill, Z Han, F Gao, G Swartz, S M Plum, L Zhang, S J Green

Department of Oncology, Georgetown University Medical Center, Washington, DC 20007 USA.

Journal Article: Cancer Research (impact factor: 7.54). 03/2001; 61(3):1022-8.

Abstract

In this study, a hyaluronan-binding complex, which we termed Metastatin, was isolated from bovine cartilage by affinity chromatography and found to have both antitumorigenic and antiangiogenic properties. Metastatin was able to block the formation of tumor nodules in the lungs of mice inoculated with B16BL6 melanoma or Lewis lung carcinoma cells. Single i.v. administration of Metastatin into chicken embryos inhibited the growth of both B16BL6 mouse melanoma and TSU human prostate cancer cells growing on the chorioallantoic membrane. The in vivo biological effect may be attributed to the antiangiogenic activity because Metastatin is able to inhibit the migration and proliferation of cultured endothelial cells as well as vascular endothelial growth factor-induced angiogenesis on the chorioallantoic membrane. In each case, the effect could be blocked by either heat denaturing the Metastatin or premixing it with hyaluronan, suggesting that its activity critically depends on its ability to bind hyaluronan on the target cells. Collectively, these results suggest that Metastatin is an effective antitumor agent that exhibits antiangiogenic activity.

Source: PubMed

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Keywords

affinity chromatography
 
antiangiogenic activity
 
antiangiogenic properties
 
antitumorigenic
 
B16BL6 melanoma
 
B16BL6 mouse melanoma
 
bind hyaluronan
 
bovine cartilage
 
chicken embryos inhibited
 
chorioallantoic membrane
 
cultured endothelial cells
 
effective antitumor agent
 
exhibits antiangiogenic activity
 
heat denaturing
 
hyaluronan-binding complex
 
Lewis lung carcinoma cells
 
mice inoculated
 
TSU human prostate cancer cells
 
tumor nodules
 
vivo biological effect