Epigallocatechin-3-gallate inhibits migration and invasion of human renal carcinoma cells by downregulating matrix metalloproteinase-2 and matrix metalloproteinase-9

被引:48
作者
Chen, Shao-Jun [1 ]
Yao, Xu-Dong [1 ]
Peng, Bo [1 ]
Xu, Yun-Fei [1 ]
Wang, Guang-Chun [1 ]
Huang, Jianhua [1 ]
Liu, Min [1 ]
Zheng, Jun-Hua [1 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Dept Urol, 301 Yanchang Rd, Shanghai 200072, Peoples R China
基金
中国国家自然科学基金;
关键词
epigallocatechin-3-gallate; renal cell carcinoma; migration; invasion; matrix metalloproteinase-2; matrix metalloproteinase-9; BREAST-CANCER CELLS; GREEN TEA; PANCREATIC-CANCER; MMP-9; EXPRESSION; METASTASIS; EGCG; GROWTH; ANGIOGENESIS; DECREASES; MICRORNAS;
D O I
10.3892/etm.2016.3050
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The anticancer properties of epigallocatechin-3-gallate (EGCG) are documented in the treatment of several types of cancer; however, there is no relevant evidence for its efficacy in the treatment of renal cell carcinoma (RCC). In the present study, the therapeutic effects of EGCG in vitro were investigated, with particular attention to the metastatic behavior of human RCC cells. MTT assays and flow cytometry were performed to detect the effects of EGCG on the proliferation and apoptosis of RCC cells. The migration and invasion abilities of RCC cells following treatment with EGCG were assessed by wound-healing and Transwell assays, respectively. Gelatin zymography and western blot analysis were performed to analyze the effect of EGCG on matrix metalloproteinase-2 (MMP-2) and MMP-9 expression levels. The results suggested that EGCG was able to inhibit the proliferation of RCC cells, induce apoptosis and effectively suppressed the migration and invasion of RCC cells. In addition, EGCG treatment resulted in the downregulation of MMP-2 and MMP-9 in RCC cells. We hypothesize that the anticancer effect associated with EGCG may involve the downregulation of MMP-2 and MMP-9. The present results suggest the potential of EGCG as a novel therapeutic agent against RCC.
引用
收藏
页码:1243 / 1248
页数:6
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