啤酒花(Humulus lupulus L.)和芒果姜(Curcuma amada Roxb.)超临界提取物对人胶质母细胞瘤的抗癌和抗转移作用

C. Ramachandran, A. Juan, K. Quirin, L. Khatib, E. Escalon, Z. Khatib, S. Melnick
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引用次数: 0

摘要

胶质母细胞瘤是人类最具侵袭性、致死性和不可治愈的原发性脑肿瘤之一,预后较差。芒果姜(Curcuma amada)和啤酒花(Humulus lupulus)是两种含有潜在抗癌作用的植物化学物质的植物药。研究了芒果姜超临界CO2萃取物(CA)和啤酒花乙醇萃取物(HL)对U-87MG人胶质母细胞瘤细胞株的抗癌和抗转移作用。CA和HL对胶质母细胞瘤细胞均表现出较强的细胞毒性。细胞毒性数据的CompuSyn分析证实CA和HL在细胞毒性方面具有协同作用,联合指数(CI)值<1.0。此外,CA和HL单独或联合显著抑制U-87MG细胞中MMP-2和MMP-9活性、肿瘤细胞迁移(跨内皮细胞迁移试验)和AKT磷酸化。CA和HL抑制U-87MG细胞的糖酵解,这表明CA+HL联合抑制ATP和乳酸合成,与单独处理的细胞相比,CA+HL联合通过减少ATP和乳酸合成来抑制糖酵解。CA和HL处理下调转移相关蛋白MMP-2和MMP-9的表达,上调TIMP1的表达。CA和HL对胶质母细胞瘤细胞的处理也能调节与凋亡、炎症和能量代谢相关的蛋白质。这些结果表明CA和HL可以联合用于胶质母细胞瘤的治疗管理。
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Anticancer and Anti-metastatic Effects of Supercritical Extracts of Hops (Humulus lupulus L.) and Mango ginger (Curcuma amada Roxb.) in Human Glioblastoma
Glioblastoma is one of the most aggressive, lethal and incurable primary brain tumors with a dismal prognosis in humans. Mango ginger (Curcuma amada) and hops (Humulus lupulus) are two botanicals containing phytochemicals with potential anticancer effects. We have investigated the anticancer and antimetastatic properties of supercritical CO2 extract of mango ginger (CA) and ethanol extract of hops (HL) in the U-87MG human glioblastoma cell line. Both CA and HL individually demonstrate strong cytotoxicity against glioblastoma cells. CompuSyn analysis of cytotoxicity data confirms that CA and HL are synergistic for cytotoxicity with combination index (CI) values of <1.0. Additionally, CA and HL individually as well as the combination significantly inhibit MMP-2 and MMP-9 activity, tumor cell migration (transendothelial cell migration assay) and AKT phosphorylation in U-87MG cells. CA and HL inhibit glycolysis in U-87MG cells as indicated by the inhibition of ATP and lactate synthesis with the CA+HL combination demonstrating strong inhibition of glycolysis via the reduction of ATP and lactate synthesis compared to cells treated by each extract alone. CA and HL treatment down regulates the expression of proteins associated with metastasis, MMP-2 and MMP-9 and up regulates the expression of TIMP1. Proteins associated with apoptosis, inflammation and energy metabolism were also modulated by CA and HL treatment of glioblastoma cells. These results suggest that CA and HL can be combined for the therapeutic management of glioblastomas.
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