作者: HONGMIN CHE , JIANRONG SONG , SHIWEN GUO , WEIWEN WANG , GUODONG GAO
DOI: 10.3892/OR.2012.2187
关键词:
摘要: Angiogenesis is crucial for the development and metastasis of human brain glioma. Based on our previous successful construction a lentivirus-mediated alphastatin (an endogenous angiogenesis inhibitor) gene transfer system findings that exhibited potent inhibitory effects migration differentiation umbilical vein endothelial cell lines (HUVECs) induced by vascular growth factor (VEGF) or basic fibroblast (bFGF) in vitro, here, we investigated effect using lentiviral vectors to overexpress in glioma cells show whether sustained long-term expression diminishes tumor xenograft model. We found transduced sustainedly secreted alphastatin, which did not affect proliferative ability cells. Furthermore, xenografts treated with recombinant lentivirus were significantly smaller compared control vascularity within tumors was evidently decreased. Our data suggest stable inhibits inhibiting angiogenesis, probable mechanism suppressing turnover VE-cadherin membrane molecules.