Title of article
γ-Tocotrienol inhibits angiogenesis of human umbilical vein endothelial cell induced by cancer cell
Author/Authors
Yang Li، نويسنده , , Wenguang Sun، نويسنده , , Huikun Liu، نويسنده , , Gui-Yun Qi، نويسنده , , Qi Wang، نويسنده , , Xiang-Rong Sun، نويسنده , , Bingqing Chen، نويسنده , , Jiaren Liu، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2011
Pages
10
From page
1127
To page
1136
Abstract
Antiangiogenic therapy mediated by food components is an established strategy for cancer chemoprevention. Growth factors play critical roles in tumor angiogenesis. A conditioned medium containing growth factors from human gastric adenocarcinoma SGC-7901 cell conditioned medium was used as an angiogenic stimulus in this study. The purpose of this study was to evaluate the inhibitory effect and possible mechanism of γ-tocotrienol on tumor angiogenesis. The results showed that γ-tocotrienol (10–40 μmol/L) significantly suppressed proliferation, migration and tube formation of human umbilical vein endothelial cells (HUVECs) induced by SGC-7901 cell conditioned medium in a dose-dependent manner. γ-Tocotrienol (800–1200 μg/egg) also inhibited new blood vessel formation on the growing chick embryo chorioallantoic membrane in a dose-dependent manner. Moreover, the inhibitory effects of γ-tocotrienol on HUVECs were correlated with inducing the apoptosis and arresting cell cycle at the G0/G1 phase at a dose of 40 μmol/L γ-tocotrienol. In addition, γ-tocotrienol inhibited angiogenesis in HUVECs by down-regulation of β-catenin, cyclin D1, CD44, phospho-VEGFR-2 and MMP-9. The antiangiogenic effects of γ-tocotrienol on HUVECs may be attributable to regulation of Wnt signaling by decreasing β-catenin expression. Thus, our results suggest that γ-tocotrienol has a potential chemopreventive agent via antiangiogenesis.
Keywords
HUVEC , ?-Tocotrienol , Angiogenesis , Wnt signaling
Journal title
The Journal of Nutritional Biochemistry
Serial Year
2011
Journal title
The Journal of Nutritional Biochemistry
Record number
1299877
Link To Document