MMP9公司
STAT蛋白
血管生成
癌症研究
STAT1
车站3
基质金属蛋白酶
化学
新生血管
转录因子
血管内皮生长因子A
斯达
生物
没食子酸表没食子酸酯
血管内皮生长因子
蛋白激酶B
药理学
细胞生物学
信号转导
下调和上调
生物化学
血管内皮生长因子受体
基因
作者
Hoyee Leong,Priya Mathur,Geoffrey L. Greene
标识
DOI:10.1007/s10549-008-0196-x
摘要
Previous studies indicate that green tea extract may inhibit breast cancer progression by blocking angiogenesis, although the molecular mechanisms are not well defined. We demonstrate that administration of Polyphenon E (Poly E), a standardized green tea extract, inhibited MDA-MB231 breast cancer and human dermal microvascular endothelial (HMVEC) cell migration and the expression of vascular endothelial growth factor (VEGF) and matrix metalloproteinase 9 (MMP9). In addition, Poly E inhibited VEGF-induced neovascularization in vivo. We also demonstrate that Poly E blocked signal transducers and activators of transcription (STAT) signaling by suppressing interferon-gamma (IFN-γ)-induced gene transcription via IFN-γ-activating sequence (GAS) elements and downstream STAT3 activation by inhibiting STAT1 and STAT3 dimerization in MDA-MB231 cells. Transient expression of constitutively active STAT3 significantly reduced the inhibitory effect of Poly E on cell migration and VEGF and MMP9 expression. Taken together, these observations indicate that green tea extract inhibits angiogenesis partly through the disruption of STAT3-mediated transcription of genes, including VEGF.
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