Leong Hoyee, Mathur Priya S, Greene Geoffrey L
The Ben May Department for Cancer Research, The University of Chicago, GCIS W325D, 929 East 57th Street, Chicago, IL 60637, USA.
Breast Cancer Res Treat. 2009 Oct;117(3):505-15. doi: 10.1007/s10549-008-0196-x. Epub 2008 Sep 28.
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-gamma)-induced gene transcription via IFN-gamma-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.
先前的研究表明,绿茶提取物可能通过阻断血管生成来抑制乳腺癌进展,尽管其分子机制尚未完全明确。我们证明,给予标准化绿茶提取物Polyphenon E(Poly E)可抑制MDA-MB231乳腺癌细胞和人真皮微血管内皮(HMVEC)细胞的迁移以及血管内皮生长因子(VEGF)和基质金属蛋白酶9(MMP9)的表达。此外,Poly E在体内抑制VEGF诱导的新生血管形成。我们还证明,Poly E通过抑制MDA-MB231细胞中干扰素-γ(IFN-γ)诱导的基因转录,经由IFN-γ激活序列(GAS)元件以及通过抑制STAT1和STAT3二聚化来阻断信号转导和转录激活因子(STAT)信号通路及下游STAT3激活。组成型活性STAT3的瞬时表达显著降低了Poly E对细胞迁移以及VEGF和MMP9表达的抑制作用。综上所述,这些观察结果表明,绿茶提取物部分通过破坏STAT3介导的包括VEGF在内的基因转录来抑制血管生成。