树状体姜黄素对MCF-7乳腺癌细胞株HOTAIR长链非编码RNA表达水平的影响

M. Mehrabi, Sara Alemohammad, Reza Dashtebozorgi, M. Tahmasebi Birgani, M. Hajjari, J. Mohammadi-Asl
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引用次数: 0

摘要

乳腺癌是女性最常见的恶性肿瘤之一。研究人员考虑用草药治疗,因为其副作用较低。姜黄素是从姜黄中提取的一种多酚,具有抗癌特性。姜黄素不溶于水,代谢迅速。建议使用纳米载体给药以克服这些限制。本研究的目的是评价姜黄素对MCF-7乳腺癌细胞系HOTAIR长链非编码RNA表达水平的影响。方法:本研究为应用基础研究。首先,将姜黄素装入树状体,利用荧光显微镜研究了树状体姜黄素进入细胞的情况。采用MTT法和细胞凋亡检测试剂盒检测细胞死亡情况。实时荧光定量PCR检测HOTAIR基因的表达。据报道,该基因在多种肿瘤中表达增加。数据分析采用GraphPad Prism V9.5统计软件,采用NOVA单向统计分析和Student t检验;结果以均数±标准差报告。结果:树突体提高了姜黄素的溶解度。处理24 h和48h后,姜黄素的有效抑制剂量分别为25和20微摩尔。发生早期凋亡的细胞百分比分别为22.97±0.03和56.22±0.05,与未处理的对照细胞相比,差异有统计学意义。20微摩尔姜黄素处理24和48h后,HOTAIR基因表达显著降低(P=0.001)。结论:这些发现提示,姜黄素可能通过降低HOTAIR基因的表达,促进乳腺肿瘤细胞程序性死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluate the Effect of Dendrosomal Curcumin on Expression Level of HOTAIR Long Noncoding RNA in MCF-7 Breast Cancer Cell Line
Introduction: Breast cancer is one of the most common malignancies in women. Treatment with herbal drugs has been considered by researchers due to the lower side effects. Curcumin is a polyphenol extracted from turmeric with confirmed anti-cancer properties. Curcumin is water-insoluble with rapid metabolism. Drug delivery using nano-carriers is suggested to overcome such limitations. The aim of this study was based on evaluating the effect of Dendrosomes curcumin on expression level of HOTAIR long noncoding RNA in MCF-7 breast cancer cell line. Methods: This study was an applied basic research. Firstly, curcumin was loaded in dendrosomes and the entry of dendrosomal curcumin into cells was studied using fluorescent microscopy.  Cell death was investigated using MTT assay and apoptosis detection kit. The expression of HOTAIR gene was measured using real-time PCR. Increased expression of this gene was reported in a wide range of tumors. The data were analyzed using GraphPad Prism V9.5 statistical software, using NOVA one-way statistical analysis and Student t-test; the results were reported as mean ± standard deviation. Results: Dendrosomes increased the solubility of curcumin. The effective inhibitory doses of dendrosomal curcumin after 24 and 48h treatment were 25 and 20 micromolar, respectively. The percent of cells undergoing early apoptosis were 22.97±0.03 and 56.22±0.05, respectively, which was statistically significant in comparison with non-treated control cells. Following 24 and 48h treatment with 20 micromolar of dendrosomal curcumin, the HOTAIR gene expression was significantly decreased (P=0.001). Conclusion: These findings suggest that dendrosomal curcumin may promote breast tumor cells toward programmed cell death by reducing HOTAIR gene expression.
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