RETRACTED ARTICLE: VEGF Silencing Inhibits Human Osteosarcoma Angiogenesis and Promotes Cell Apoptosis via PI3K/AKT Signaling Pathway

被引:0
|
作者
Jian Zhao
Zi-Ru Zhang
Na Zhao
Bao-An Ma
Qing-Yu Fan
机构
[1] Fourth Military Medical University,Department of Orthopedic Surgery, Tangdu Hospital, Orthopedics Oncology Institute of Chinese PLA
[2] Fourth Military Medical University,Outpatient Department, Tangdu Hospital
来源
Cell Biochemistry and Biophysics | 2015年 / 73卷
关键词
Cell apoptosis; Angiogenesis; Lentivirus-mediated short hairpin RNA (Lv-shRNA); U2OS cells; Vascular endothelial growth factor (VEGF);
D O I
暂无
中图分类号
学科分类号
摘要
Vascular endothelial growth factor (VEGF) is one of the most effective angiogenic factors that promote generation of tumor vasculature. VEGF is usually up-regulated in multiple cancers including osteosarcoma and glioma. To further explore the potential molecular mechanism that inhibits tumor growth induced by interference of VEGF expression, we constructed a Lv-shVEGF vector and assessed the efficiency of VEGF silencing and its influence in U2OS cells. The data demonstrate that Lv-shVEGF has high inhibition efficiency on VEGF expression, which inhibits proliferation and promotes apoptosis of U2OS cells in vitro. Our results also indicate that inhibition of VEGF expression suppresses osteosarcoma tumor growth in vivo and reduces osteosarcoma angiogenesis. We also found that the activations of phosphoinositide 3-kinase (PI3K) and protein kinase B (AKT) were considerably reduced after osteosarcoma cells were treated with Lv-shVEGF. Taken together, our data demonstrate that VEGF silencing suppresses cell proliferation, promotes cell apoptosis, and reduces osteosarcoma angiogenesis through inactivation of PI3K/AKT signaling pathway.
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页码:519 / 525
页数:6
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