Epigallocatechin-3 Gallate Inhibits Invasion, Epithelial-Mesenchymal Transition, and Tumor Growth in Oral Cancer Cells

被引:76
|
作者
Chen, Pei-Ni [2 ,6 ]
Chu, Shu-Chen [1 ]
Kuo, Wu-Hsien [4 ,5 ]
Chou, Ming-Yung [7 ]
Lin, Jen-Kun [8 ]
Hsieh, Yih-Shou [3 ,6 ]
机构
[1] Cent Taiwan Univ Sci & Technol, Inst & Dept Food Sci, Taichung 406, Taiwan
[2] Chung Shan Med Univ, Inst Biochem & Biotechnol, Taichung, Taiwan
[3] Chung Shan Med Univ, Dept Biochem, Taichung, Taiwan
[4] Cent Taiwan Univ Sci & Technol, Gen Educ Ctr, Taichung 406, Taiwan
[5] Armed Force Taichung Gen Hosp, Dept Internal Med, Div Gastroenterol, Taichung, Taiwan
[6] Chung Shan Med Univ Hosp, Clin Lab, Taichung, Taiwan
[7] Chung Shan Med Univ Hosp, Dept Dent, Taichung, Taiwan
[8] Natl Taiwan Univ, Coll Med, Inst Biochem & Mol Biol, Taipei 10764, Taiwan
关键词
EMT; EGCG; invasion; MMP; u-PA; NF-KAPPA-B; FIBROSARCOMA HT1080 CELLS; MATRIX METALLOPROTEINASES; DOWN-REGULATION; GREEN TEA; MAPK PATHWAY; PROTEINASES ACTIVITIES; PANCREATIC-CANCER; IN-VITRO; METASTASIS;
D O I
10.1021/jf1049408
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Epithelial to mesenchymal transition (EMT) is critical for the progression, invasion, and metastasis of epithelial tumorgenesis. Here, we provided molecular evidence associated with the antimetastatic effect of green tea polyphenol epigallocatechin-3 gallate (EGCG) in an oral squamous cell culture system by showing a nearly complete inhibition on the invasion (P < 0.001) of squamous cell carcinoma-9 (SCC-9) cells via a reduced expression of matrix metalloproteinase-2 (P < 0.001) and urokinasetype plasminogen activator (P < 0.001). EGCG exerted an inhibitory effect on cell migration (P < 0.001), motility (P < 0.001), spread, and adhesion (P < 0.001). We performed Western blot to find that EGCG inhibited p-focal adhesion kinase (p-FAK), p-Src, snail-1, and vimentin, indicating the anti-EMT effect of EGCG in oral squamous cell carcinoma. EGCG was also sufficient to inhibit phorbol-12-myristate-13-acetate-induced cell invasion and matrix metalloproteinase-9 expression, as evidenced by its inhibition on the tumor growth of SCC-9 cells in vivo via cancer cell xenografted nude mice mode. These results suggested that EGCG could reduce the invasion and cell growth of tumor cells, and such a characteristic may be of great value in developing a potential cancer therapy.
引用
收藏
页码:3836 / 3844
页数:9
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