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Fucoidan Extract Enhances the Anti-Cancer Activity of Chemotherapeutic Agents in MDA-MB-231 and MCF-7 Breast Cancer Cells

机译:岩藻依聚糖提取物增强MDA-MB-231和MCF-7乳腺癌细胞中化学治疗剂的抗癌活​​性。

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Fucoidan, a fucose-rich polysaccharide isolated from brown alga, is currently under investigation as a new anti-cancer compound. In the present study, fucoidan extract (FE) from Cladosiphon navae-caledoniae Kylin was prepared by enzymatic digestion. We investigated whether a combination of FE with cisplatin, tamoxifen or paclitaxel had the potential to improve the therapeutic efficacy of cancer treatment. These co-treatments significantly induced cell growth inhibition, apoptosis, as well as cell cycle modifications in MDA-MB-231 and MCF-7 cells. FE enhanced apoptosis in cancer cells that responded to treatment with three chemotherapeutic drugs with downregulation of the anti-apoptotic proteins Bcl-xL and Mcl-1. The combination treatments led to an obvious decrease in the phosphorylation of ERK and Akt in MDA-MB-231 cells, but increased the phosphorylation of ERK in MCF-7 cells. In addition, we observed that combination treatments enhanced intracellular ROS levels and reduced glutathione (GSH) levels in breast cancer cells, suggesting that induction of oxidative stress was an important event in the cell death induced by the combination treatments.
机译:岩藻糖聚糖是一种从褐藻中分离出的富含岩藻糖的多糖,目前正作为一种新的抗癌化合物进行研究。在本研究中,通过酶消化制备了克拉多水藻-卡德多尼亚麒麟菜中的岩藻依聚糖提取物(FE)。我们调查了FE与顺铂,他莫昔芬或紫杉醇的组合是否具有改善癌症治疗疗效的潜力。这些共同处理显着诱导了MDA-MB-231和MCF-7细胞的细胞生长抑制,凋亡以及细胞周期修饰。 FE增强了癌细胞的凋亡,该癌细胞对三种化疗药物的治疗均具有抗凋亡蛋白Bcl-xL和Mcl-1的下调。联合处理导致MDA-MB-231细胞中ERK和Akt的磷酸化明显降低,但增加了MCF-7细胞中ERK的磷酸化。此外,我们观察到联合治疗可提高乳腺癌细胞的细胞内ROS水平并降低谷胱甘肽(GSH)水平,这表明氧化应激的诱导是联合治疗所致细胞死亡的重要事件。

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