Feng Chenchen, Ho Yatfaat, Sun Chuanyu, Xia Guowei, Ding Qiang, Gu Bin
Department of Urology, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Exp Ther Med. 2017 Oct;14(4):3513-3518. doi: 10.3892/etm.2017.4981. Epub 2017 Aug 21.
Epigallocatechin gallate (EGCG) has been revealed to inhibit the proliferation and induce the apoptosis of several types of tumor, in addition to inhibiting DNA methyltransferase activity, leading to CpG demethylation. Tissue factor pathway inhibitor 2 (TFPI-2) expression is downregulated in bladder cancer. The present study revealed that this downregulation was partly due to hypermethylation of the TFPI-2 gene promoter, which was decreased by EGCG treatment. In addition, the present study demonstrated that EGCG could inhibit the viability and invasion, and induce the apoptosis, of bladder cancer T24 cells. Furthermore, western blot analysis and reverse transcription-quantitative polymerase chain reaction analyses demonstrated that EGCG could upregulate the expression of TFPI-2. These results suggest that EGCG inhibits the growth and induces the apoptosis of bladder cancer cells through restoring TFPI-2 expression. Thus, EGCG is a potential therapeutic candidate for the treatment of bladder cancer.
表没食子儿茶素没食子酸酯(EGCG)已被证实除了能抑制DNA甲基转移酶活性导致CpG去甲基化外,还能抑制多种肿瘤的增殖并诱导其凋亡。组织因子途径抑制剂2(TFPI-2)在膀胱癌中表达下调。本研究表明,这种下调部分归因于TFPI-2基因启动子的高甲基化,而EGCG处理可使其降低。此外,本研究证明EGCG可抑制膀胱癌T24细胞的活力和侵袭,并诱导其凋亡。此外,蛋白质印迹分析和逆转录-定量聚合酶链反应分析表明,EGCG可上调TFPI-2的表达。这些结果表明,EGCG通过恢复TFPI-2的表达来抑制膀胱癌细胞的生长并诱导其凋亡。因此,EGCG是治疗膀胱癌的潜在候选药物。