An investigation of the anti-cancer effects of vitamin D on the expression of HE4 gene and the viability of ovarian cancer cell line A2780S

Maryam Yahyaie, E. Salehi, Majid Morovati-Sharifabad, F. Sarkargar, M. S. Heydarnejad, G. Pourghanbari
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Abstract

Background and aims: Ovarian cancer is the second most common cause of death in Iran. A reduction in vitamin D production has been associated with an increased risk for ovarian cancer in many studies. Human epididymis protein 4 (HE4) is known as one of the most accurate tumor markers for the analysis of ovarian epithelial cancer illness or progression. The expression of the gene increases in many types of ovarian cancer. The aim of this study was to find whether vitamin D has anticancer effects on the viability of HE4 gene expression. Methods: The human ovarian cancer cell line (A2780S) was cultured in an RPMI-1640 medium. To determine the inhibitory concentration (IC50), the cells were treated with various concentrations of vitamin D and then incubated for 24, 48, and 72 hours. The effect of drugs on the expression of HE4 gene modification was measured and evaluated using the real-time polymerase chain reaction and a 2-ΔΔCT method, respectively. Results: The IC50 value for vitamin D was 0.359 μM, and the maximum death rates were observed after 24 hours (56.20 ± 5.79). The HE4 gene expression treated with vitamin D increased compared with the cells in the control group (Fold change > 1). Conclusion: Vitamin D decreases the viability of A2780S cells, whereas the expression of the HE4 gene is improved in cells treated with vitamin D compared to control cells, indicating that vitamin D may be unable to modify A2780S cells.
维生素D对卵巢癌细胞系A2780S HE4基因表达及细胞活力的影响
背景和目的:卵巢癌是伊朗第二大常见死因。在许多研究中,维生素D生成的减少与卵巢癌风险的增加有关。人附睾蛋白4 (HE4)被认为是卵巢癌发病或进展最准确的肿瘤标志物之一。该基因的表达在许多类型的卵巢癌中增加。本研究的目的是发现维生素D是否对HE4基因表达的活力有抗癌作用。方法:在RPMI-1640培养基中培养人卵巢癌细胞系A2780S。为了测定细胞的抑制浓度(IC50),将细胞用不同浓度的维生素D处理,然后孵育24、48和72小时。采用实时聚合酶链反应法和2-ΔΔCT法分别检测和评价药物对HE4基因修饰表达的影响。结果:维生素D的IC50值为0.359 μM, 24 h死亡率最高(56.20±5.79)。与对照组相比,维生素D处理的细胞HE4基因表达增加(Fold change > 1)。结论:维生素D降低了A2780S细胞的活力,而维生素D处理的细胞HE4基因表达较对照细胞有所提高,说明维生素D可能无法修饰A2780S细胞。
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