Belguise Karine, Guo Shangqin, Sonenshein Gail E
Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts 02118, USA.
Cancer Res. 2007 Jun 15;67(12):5763-70. doi: 10.1158/0008-5472.CAN-06-4327.
Previously, we showed that the bioactive green tea polyphenol epigallocatechin-3-gallate (EGCG) inhibits growth in soft agar of breast cancer cells with Her-2/neu overexpression. Using gene expression profiling, here we show that EGCG treatment of Her-2/neu-driven mammary tumor cells alters the expression of key regulators in the epithelial to mesenchymal transition (EMT) pathway, reducing invasive phenotype. Specifically, the epithelial genes E-cadherin, gamma-catenin, MTA3, and estrogen receptor alpha (ERalpha) were up-regulated by EGCG, whereas the proinvasive snail gene was down-regulated. Consistently, EGCG inhibited branching colony growth and invasion in Matrigel. EGCG treatment similarly inhibited invasive phenotype of mouse mammary tumor cells driven by Nuclear Factor-kappaB c-Rel and protein kinase CK2, frequently found overexpressed in human breast disease. Recently, we identified the Forkhead box O transcription factor FOXO3a as a major transcriptional regulator of ERalpha. Given the pivotal role of ERalpha in preventing EMT, we hypothesized that the activation of FOXO3a by EGCG plays an important role in the observed reversal of invasive phenotype in ERalpha-positive breast cancer cells. EGCG treatment activated FOXO3a. Ectopic expression of a constitutively active FOXO3a overrode transforming growth factor-beta1-mediated invasive phenotype and induced a more epithelial phenotype, which was dependent on ERalpha expression and signaling. Conversely, a dominant negative FOXO3a reduced epithelial phenotype of ERalpha-low breast cancer cells. These results identify, for the first time, a role for FOXO3a in the inhibition of invasive phenotype in breast cancer cells with active ERalpha signaling and elucidate a novel mechanism whereby EGCG represses EMT of breast cancer cells.
此前,我们发现具有生物活性的绿茶多酚表没食子儿茶素-3-没食子酸酯(EGCG)可抑制Her-2/neu过表达的乳腺癌细胞在软琼脂中的生长。利用基因表达谱分析,我们在此表明,EGCG处理Her-2/neu驱动的乳腺肿瘤细胞可改变上皮-间质转化(EMT)途径中关键调节因子的表达,降低侵袭表型。具体而言,EGCG可上调上皮基因E-钙黏蛋白、γ-连环蛋白、MTA3和雌激素受体α(ERα),而下调促侵袭的蜗牛基因。同样,EGCG可抑制基质胶中分支集落的生长和侵袭。EGCG处理同样可抑制由核因子κB c-Rel和蛋白激酶CK2驱动的小鼠乳腺肿瘤细胞的侵袭表型,这两种因子在人类乳腺疾病中常过度表达。最近,我们确定叉头框O转录因子FOXO3a是ERα的主要转录调节因子。鉴于ERα在预防EMT中的关键作用,我们推测EGCG对FOXO3a的激活在ERα阳性乳腺癌细胞侵袭表型的逆转中起重要作用。EGCG处理可激活FOXO3a。组成型活性FOXO3a的异位表达可克服转化生长因子-β1介导的侵袭表型,并诱导更上皮化的表型,这依赖于ERα的表达和信号传导。相反,显性负性FOXO3a可降低ERα低表达乳腺癌细胞的上皮表型。这些结果首次确定了FOXO3a在抑制具有活跃ERα信号传导的乳腺癌细胞侵袭表型中的作用,并阐明了EGCG抑制乳腺癌细胞EMT的新机制。