Department of Pathology, School of Dentistry, Chosun University, Dong-gu, Gwangju, Korea.
Oncol Rep. 2010 Feb;23(2):585-90.
(-)-Epigallocatechin-3-gallate (EGCG) has inhibitory effect on a variety of cancers by inducing apoptosis and cell cycle arrest or inhibiting angiogenesis and metastasis. EGCG has been found to induce apoptosis in salivary gland carcinoma cells, however, it is not known whether EGCG affects invasion and migration. Thus, this study was performed to clarify whether EGCG affects invasion and migration of salivary gland tumors. Matrigel invasion assay, wound scratch assay and migration assay using commercial kit were performed. beta1 integrin expression and activation of its downstream molecules such as focal adhesion kinase (FAK), AKT and extracellular signal-regulated kinase (ERK) were examined by Western blot. Enzymatic activity of matrix metalloprotease (MMP)-2 and MMP-9 was examined by gelatin zymography. EGCG inhibited effectively invasion and migration of SGT cells in a dose-dependent manner. EGCG also inhibited the activation of beta1 integrin-downstream molecules such as FAK, AKT and ERK as well as the expression of beta1 integrin itself. Moreover, MMP-2 and MMP-9 expression and their enzymatic activity were reduced by EGCG in a dose-dependent manner. These results indicate that EGCG may effectively suppress salivary gland tumors by inhibiting metastasis through beta1 integrin-mediated signaling.
(-)-表没食子儿茶素没食子酸酯(EGCG)通过诱导细胞凋亡和细胞周期停滞或抑制血管生成和转移,对多种癌症具有抑制作用。已经发现 EGCG 可诱导唾液腺癌细胞凋亡,但尚不清楚 EGCG 是否影响侵袭和迁移。因此,本研究旨在阐明 EGCG 是否影响唾液腺肿瘤的侵袭和迁移。进行了 Matrigel 侵袭测定、划痕实验和使用商业试剂盒的迁移测定。通过 Western blot 检查了β1 整合素表达及其下游分子如粘着斑激酶(FAK)、AKT 和细胞外信号调节激酶(ERK)的激活。通过明胶酶谱法检查了基质金属蛋白酶(MMP)-2 和 MMP-9 的酶活性。EGCG 以剂量依赖性方式有效抑制 SGT 细胞的侵袭和迁移。EGCG 还抑制了β1 整合素下游分子如 FAK、AKT 和 ERK 的激活以及β1 整合素本身的表达。此外,EGCG 以剂量依赖性方式减少 MMP-2 和 MMP-9 的表达及其酶活性。这些结果表明,EGCG 可能通过β1 整合素介导的信号转导有效抑制唾液腺癌的转移,从而有效抑制唾液腺肿瘤。