Acacetin inhibits VEGF expression, tumor angiogenesis and growth through AKT/HIF-1α pathway

被引:47
作者
Liu, Ling-Zhi [1 ]
Jing, Yi [1 ]
Jiang, Lisa L. [2 ]
Jiang, Xiu-E [2 ]
Jiang, Yue [1 ]
Rojanasakul, Yongyut [2 ]
Jiang, Bing-Hua [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[2] W Virginia Univ, Dept Pharmaceut Sci, Morgantown, WV 26506 USA
关键词
Acacetin; VEGF; Angiogenesis; HIF-1; AKT; HYPOXIA-INDUCIBLE FACTOR-1; CELL-CYCLE PROGRESSION; PROSTATE-CANCER CELLS; HUMAN LUNG-CANCER; SIGNALING PATHWAY; FACTOR GENE; ACTIVATION; APOPTOSIS; FLAVONOIDS; APIGENIN;
D O I
10.1016/j.bbrc.2011.08.091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acacetin (5.7-dihydroxy-4'-methoxyflavone) is a flavone compound, some of which have anti-cancerous effects. Vascular endothelial growth factor (VEGF) plays an important role in angiogenesis and tumor growth. In this study, we found that acacetin decreased the steady level of VEGF mRNA level and inhibited VEGF transcriptional activation. To further determine the potential mechanism of acacetin in inhibiting VEGF expression, we showed that acacetin inhibited HIF-1 alpha expression and AKT activation. Overexpression of HIF-1 alpha or AKT restored acacetin-decreasing VEGF transcriptional activation, indicating that AKT and HIF-1 are the essential downstream targets of acacetin for inhibiting VEGF expression in the cells. Moreover, acacetin significantly inhibited ovarian cancer cell-induced angiogenesis and tumor growth in vivo through inhibiting HIF-1 alpha and VEGF expression. Acacetin did not change HIF-1 alpha mRNA level, but inhibited HIF-1 alpha protein level through increasing its degradation and decreasing its stability. These results indicate that acacetin may be a useful natural compound for ovarian cancer prevention and treatment. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:299 / 305
页数:7
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