Zerumbone (ZER), a Potential Anticancer for Breast Mediates Cancer Cell Death Through Targeting β-catenin Signaling Pathway in MCF-7 Cell Line

I. Arbab, Abdirahman Hussein Adan, Dalia Younis Adam Haroon, Salah Eldeen H. Abdlrazig, Mohamed A. Bakr, Ahmed Isse Mohamud, Fath Elrahman Abaid Alla Ali, Daralsalalam Essmael Mohammed, Awad Salim Ibrahim Holy
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Abstract

Background: Zerumbone is a sesquiterpene which was found to delay progression of breast cancer through apoptosis induction via up-regulating Bax protein and down-regulating Bcl2 protein. Purpose: In this study, we aimed to investigate Zerumbone, a natural compound of medicinal herbal plant isolated from Zingiber zerumbet, for anti-cancer activity against MCF-7 cell line. Methods: Human cancer cell lines of breast MCF-7 cells were obtained from American Type Culture Collection (ATCC, Manassas, VA). ON target plus smart pool siRNA, the most efficient method is used for preparation of β-catenin siRNA. Cyclophilin B siRNA is considered as positive control. Zrumbone is an ethanol-soluble compound isolated from Zingiber zerumbet, extracted by the hydro-distillation (steam distillation) method. Purification of ZER was examined using HPLC. The MCF-7 cells transfected with 100 µM human β-catenin (CTNNB1) siRNA or cyclophilin B siRNA positive control. After transfection, the cells were harvested at 48hrs for mRNA analysis or 48 – 72 hrs for protein analysis. IC50 for ZER was determined using MTT assay. MCF-7 transfected with β-catenin siRNA were then treated with ZER IC50. The mRNA expression was analyzed using real-time to ensure the knock down of β-catenin. TUNNEL assay was used to confirm apoptosis and flow cytometry was applied for quantification of apoptotic cells. Western blot analysis was done to evaluate the effect of ZER and β-catenin (CTNNB1) siRNA on the expression of β-catenin and its functional impact on the proliferation and survival of MCF-7 cells. Results: ZER decreased β-catenin protein expression in breast cancer cell lines. ZER downregulated β-catenin mRNA level in breast cancer cell lines. Depletion of β-catenin by β-catenin siRNA and ZER induce cell apoptosis. Apoptosis caused by ZER was confirmed/examined using by annexin V (annexin V was used as a marker for drug action). Conclusion: Zerumbone possesses anti-breast cancer activity, which could be attributed to the reduction of β-catenin protein expression in MCF-7 breast cancer cell lines, downregulation of β-catenin mRNA level in breast cancer cell lines and through annexin V.
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Zerumbone (ZER)--一种潜在的乳腺癌抗癌药物--通过靶向 MCF-7 细胞系中的β-catenin 信号通路介导癌细胞死亡
背景:研究发现,Zerumbone 是一种倍半萜,可通过上调 Bax 蛋白和下调 Bcl2 蛋白诱导细胞凋亡,从而延缓乳腺癌的进展。目的:本研究旨在研究从 Zingiber zerumbet 中分离出的一种药用植物天然化合物 Zerumbone 对 MCF-7 细胞株的抗癌活性。方法:人乳腺癌细胞株 MCF-7 细胞取自美国类型培养物保藏中心(ATCC,Manassas,VA)。在制备β-catenin siRNA时,采用了最有效的ON target plus smart pool siRNA方法。Cyclophilin B siRNA 被视为阳性对照。Zrumbone 是一种从 Zingiber zerumbet 中分离出来的乙醇可溶性化合物,通过水蒸气蒸馏法提取。使用高效液相色谱法检测了 ZER 的纯化情况。用 100 µM 人 β-catenin(CTNNB1)siRNA 或 cyclophilin B siRNA 阳性对照转染 MCF-7 细胞。转染后,48 小时收获细胞进行 mRNA 分析,48 - 72 小时收获细胞进行蛋白质分析。使用 MTT 试验测定 ZER 的 IC50。用 β-catenin siRNA 转染 MCF-7 后,再用 ZER IC50 处理。实时分析 mRNA 表达,以确保β-catenin 被敲除。TUNNEL检测用于确认细胞凋亡,流式细胞术用于定量凋亡细胞。采用 Western 印迹分析评估 ZER 和 β-catenin (CTNNB1) siRNA 对 β-catenin 表达的影响及其对 MCF-7 细胞增殖和存活的功能性影响。结果ZER能降低乳腺癌细胞株中β-catenin蛋白的表达。ZER 下调了乳腺癌细胞株中 β-catenin mRNA 的水平。通过β-catenin siRNA和ZER消耗β-catenin可诱导细胞凋亡。通过附件素 V(附件素 V 被用作药物作用的标志物)证实/检测了 ZER 引起的细胞凋亡。结论泽润邦具有抗乳腺癌活性,这可能是由于泽润邦降低了MCF-7乳腺癌细胞株中β-catenin蛋白的表达,下调了乳腺癌细胞株中β-catenin mRNA的水平,并通过annexin V诱导细胞凋亡。
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