Department of Biochemistry, Faculty of Medicine, Birjand University of Medical Sciences, Birjand, Iran.
Department of Biochemistry, Faculty of Medicine, Ahvaz Jundishapur University of Medical sciences, Ahvaz, Iran.
Mol Biol Rep. 2023 Sep;50(9):7225-7236. doi: 10.1007/s11033-023-08616-w. Epub 2023 Jul 7.
Estrogen receptor (ER) is a transcription factor that affects the expression of some genes involved in the progression and development of breast cancer (BC). Hesperetin (Hst) is a flavonoid that inhibits the proliferation of BC cells. In this study, we investigated the effect of Hst on the cell viability of MCF-7 cells and the gene expression of the ERα, ERβ, IL-6, Ps2, and Cyclin D1.
In this study, cell viability was determined by MTT assay. The cells were seeded in RPMI-1640 medium and then exposed to different concentrations of Hst (0, 25, 50, 100, 200, and 400 µM) for 24 h, and IC50 was calculated. Real-time PCR was used to assess the expression of ERα, ERβ, pS2, Cyclin D1, and IL-6 mRNA. MCF-7 cells were seeded in RPMI-1640 medium and then exposed to different concentrations of Hst (0, 25, 50, 100, and 200 µM) for 24 h. Real-time PCR was carried out using a Step One Real-Time PCR System (ABI, USA) and Amplicon SYBR Green reagents.
The MTT assay revealed increased cytotoxicity with higher concentrations of Hst, and the IC was calculated at 200 µM. Real-time PCR analysis following treatment with Hst showed a significant increase in ERα gene expression at 25 µM of Hst and a decrease in expression at 50, 100, and 200 µM of Hst (p < 0.0001). ERβ gene expression significantly decreased across all concentrations of Hst (p < 0.0001), while IL-6 gene expression decreased significantly in all concentrations (p < 0.0001). pS2 gene expression increased significantly with all concentrations of Hst (p < 0.0001), while Cyclin D1 gene expression did not significantly decrease upon Hst exposure (p > 0.05).
The results of our study demonstrate that Hst has the ability to induce cell death in MCF-7 cells. Furthermore, it was observed that Hst reduces the expression of the ER gene and enhances its activity, which can affect the downstream pathways of the ER.
雌激素受体(ER)是一种转录因子,影响参与乳腺癌(BC)进展和发展的一些基因的表达。橙皮素(Hst)是一种黄酮类化合物,可抑制 BC 细胞的增殖。在这项研究中,我们研究了 Hst 对 MCF-7 细胞活力和 ERα、ERβ、IL-6、Ps2 和 Cyclin D1 基因表达的影响。
在这项研究中,通过 MTT 测定法测定细胞活力。将细胞接种在 RPMI-1640 培养基中,然后用不同浓度的 Hst(0、25、50、100、200 和 400µM)处理 24 小时,计算 IC50。使用实时 PCR 评估 ERα、ERβ、pS2、Cyclin D1 和 IL-6 mRNA 的表达。将 MCF-7 细胞接种在 RPMI-1640 培养基中,然后用不同浓度的 Hst(0、25、50、100 和 200µM)处理 24 小时。使用 Step One Real-Time PCR 系统(ABI,美国)和 Amplicons SYBR Green 试剂进行实时 PCR。
MTT 测定显示,随着 Hst 浓度的增加,细胞毒性增加,IC 为 200µM。用 Hst 处理后进行实时 PCR 分析显示,在 25µM 的 Hst 下 ERα 基因表达显著增加,而在 50、100 和 200µM 的 Hst 下表达减少(p<0.0001)。所有浓度的 Hst 均显著降低 ERβ 基因表达(p<0.0001),而 IL-6 基因表达在所有浓度下均显著降低(p<0.0001)。pS2 基因表达随 Hst 浓度的增加而显著增加(p<0.0001),而 Cyclin D1 基因表达在 Hst 暴露后并未显著降低(p>0.05)。
我们的研究结果表明,Hst 具有诱导 MCF-7 细胞死亡的能力。此外,观察到 Hst 降低 ER 基因的表达并增强其活性,这可能会影响 ER 的下游途径。