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绿茶提取物对人平滑肌瘤细胞增殖的抑制作用是通过儿茶酚-O-甲基转移酶介导的。

Green tea extract inhibition of human leiomyoma cell proliferation is mediated via catechol-O-methyltransferase.

作者信息

Zhang Dong, Rajaratnam Veera, Al-Hendy Omar, Halder Sunil, Al-Hendy Ayman

机构信息

Center for Women's Health Research, Meharry Medical College, Nashville, Tenn., USA.

出版信息

Gynecol Obstet Invest. 2014;78(2):109-18. doi: 10.1159/000363410. Epub 2014 Jun 18.

Abstract

BACKGROUND/AIMS: To investigate the inhibitory effect of green tea extract, epigallocatechin gallate (EGCG), on wild-type human leiomyoma (WT-HuLM) cells and its potential action via catechol-o-methyltransferase (COMT) activity.

METHODS

Cell proliferation of WT-HuLM and COMT gene-silenced HuLM (COMT-shRNA-HuLM) cells treated with 0 or 100 µM EGCG for 7 days was measured using the MTT method. Total RNA and protein were extracted from cells treated with 0 or 100 µM of EGCG for 48 h. Gene expression profiling was performed using Human Signal Transduction PathwayFinder. Proliferation cell nuclear antigen (PCNA), cyclin-dependent kinase 4 (Cdk4) and COMT protein levels were detected by Western blot analyses. COMT enzyme activity was evaluated by HPLC.

RESULTS

EGCG-treated WT-HuLM cells showed significantly decreased COMT expression (p < 0.001) and enzyme activity (p < 0.05) compared to untreated WT-HuLM cells, while COMT-shRNA-HuLM cells showed no significant change. At 100 μM of EGCG, survival of WT-HuLM cells was significantly lower (p < 0.05) compared to COMT-shRNA-HuLM cells. EGCG treatment modulated multiple signaling pathways in WT-HuLM compared to untreated control, while changes were minimal or reversed in COMT-shRNA-HuLM cells. EGCG significantly decreased PCNA, Cdk4 and soluble COMT protein levels (p < 0.001) in WT-HuLM, but not in COMT-shRNA-HuLM cells.

CONCLUSIONS

The antiproliferative and gene-modulating effects of EGCG on HuLM cells are mediated, at least partially, via its effect on COMT expression and enzyme activity.

摘要

背景/目的:研究绿茶提取物表没食子儿茶素没食子酸酯(EGCG)对野生型人平滑肌瘤(WT-HuLM)细胞的抑制作用及其通过儿茶酚-O-甲基转移酶(COMT)活性发挥的潜在作用。

方法

采用MTT法检测用0或100 μM EGCG处理7天的WT-HuLM细胞和COMT基因沉默的HuLM细胞(COMT-shRNA-HuLM)的细胞增殖情况。从用0或100 μM EGCG处理48小时的细胞中提取总RNA和蛋白质。使用人类信号转导通路检测试剂盒进行基因表达谱分析。通过蛋白质免疫印迹分析检测增殖细胞核抗原(PCNA)、细胞周期蛋白依赖性激酶4(Cdk4)和COMT蛋白水平。通过高效液相色谱法评估COMT酶活性。

结果

与未处理的WT-HuLM细胞相比,EGCG处理的WT-HuLM细胞显示COMT表达显著降低(p < 0.001)和酶活性降低(p < 0.05),而COMT-shRNA-HuLM细胞无显著变化。在100 μM EGCG时,WT-HuLM细胞的存活率显著低于COMT-shRNA-HuLM细胞(p < 0.05)。与未处理的对照相比,EGCG处理调节了WT-HuLM中的多种信号通路,而在COMT-shRNA-HuLM细胞中变化最小或相反。EGCG显著降低了WT-HuLM中PCNA、Cdk4和可溶性COMT蛋白水平(p < 0.001),但在COMT-shRNA-HuLM细胞中未降低。

结论

EGCG对HuLM细胞的抗增殖和基因调节作用至少部分是通过其对COMT表达和酶活性的影响介导的。

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