Choi Eun Jeong, Jung Jae Yeon, Kim Gun-Hee
Plant Resources Research Institute, Duksung Women's University, Seoul 132-714, Republic of Korea.
Exp Ther Med. 2014 Aug;8(2):454-458. doi: 10.3892/etm.2014.1771. Epub 2014 Jun 10.
The present study investigated the effect of the phytochemical genistein on the proliferation and differentiation of MCF-7 and 3T3-L1 cells via the regulation of estrogen receptor-α (ERα) expression and the induction of apoptosis. When MCF-7 human breast cancer cells were treated with 50, 100, 150 and 200 μM genistein for 24, 48 or 72 h, cell growth was significantly decreased in a concentration-dependent manner. Notably, the patterns of ERα expression and proliferation in MCF-7 cells treated with genistein were similar. Furthermore, ERα expression in differentiating 3T3-L1 cells was significantly inhibited by 48 h treatment with 50 μM genistein, which was selected based on the results of cytotoxicity assays on 3T3-L1 preadipocytes [lactate dehydrogenase (LDH) and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) viability assays]. Under the same conditions, genistein-induced apoptotic features were observed in MCF-7 and differentiating 3T3-L1 cells. This observation is supported by the finding that B-cell lymphoma 2 (Bcl-2) expression was reduced while that of Bcl-2-associated X protein (Bax) was induced by genistein. The results of the present study suggest that an ERα-related pathway and the induction of apoptosis are involved in the proliferation of MCF-7 cells and the differentiation of 3T3-L1 cells.
本研究通过调节雌激素受体α(ERα)的表达和诱导细胞凋亡,研究了植物化学物质染料木黄酮对MCF-7和3T3-L1细胞增殖与分化的影响。当用50、100、150和200μM染料木黄酮处理MCF-7人乳腺癌细胞24、48或72小时时,细胞生长以浓度依赖的方式显著降低。值得注意的是,用染料木黄酮处理的MCF-7细胞中ERα表达和增殖模式相似。此外,基于对3T3-L1前脂肪细胞的细胞毒性试验[乳酸脱氢酶(LDH)和3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)活力试验]结果,选择50μM染料木黄酮处理分化中的3T3-L1细胞48小时,ERα表达受到显著抑制。在相同条件下,在MCF-7和分化中的3T3-L1细胞中观察到染料木黄酮诱导的凋亡特征。这一观察结果得到以下发现的支持:染料木黄酮可降低B细胞淋巴瘤2(Bcl-2)的表达,同时诱导Bcl-2相关X蛋白(Bax)的表达。本研究结果表明,与ERα相关的途径和凋亡诱导参与了MCF-7细胞的增殖和3T3-L1细胞的分化。