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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Fucoidan from Laminaria japonica exerts antitumor effects on angiogenesis and micrometastasis in triple-negative breast cancer cells
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Fucoidan from Laminaria japonica exerts antitumor effects on angiogenesis and micrometastasis in triple-negative breast cancer cells

机译:来自Laminaria japonica的Fucoinean对三阴性乳腺癌细胞中的血管生成和微转移产生抗肿瘤作用

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摘要

Fucoidan is a fucose-rich polysaccharide that has gained attention for its various anticancer properties. However, the effect and underlying mechanism of fucoidan on triple-negative breast cancer (TNBC) are still unknown. Herein, we investigated the anticancer potential of fucoidan from Laminaria japonica. We found that fucoidan showed modest antiproliferative activity against TNBC cells, while it effectively reduced migratory and invasive capacities. Mechanistically, fucoidan suppressed activation of MAPK and PI3K followed by inhibition of AP-1 and NF-kappa B signaling in TNBC. Additionally, fucoidan downregulated expressions of proangiogenic factors in TNBC cells, and fucoidan blocked tumor-elicited tube formation by human umbilical vascular endothelial cells (HUVECs). We also observed that fucoidan blocked tumor adhesion and invasion towards HUVECs. Surprisingly, fucoidan robustly suppressed tube formation on HUVECs. Moreover, fucoidan inhibited in vivo angiogenesis and micrometastasis in a transgenic zebrafish model. Together, L. japonica fucoidan exhibits potent antitumor effects by its attenuation of invasiveness and proangiogenesis in TNBC. (C) 2020 Elsevier B.V. All rights reserved.
机译:Fucoinean是一种富含岩石的多糖,对其各种抗癌性能进行了关注。然而,Fucoinean对三重阴性乳腺癌(TNBC)的影响和潜在机制仍然未知。在此,我们研究了来自Laminaria japonica的岩藻糖糖的抗癌潜力。我们发现Fucoidan对TNBC细胞显示适度的抗增殖活性,而它有效降低了迁移和侵入性能力。机械地,岩藻浮糖抑制MAPK和PI3K的活化,然后抑制TNBC中的AP-1和NF-Kappa B信号。另外,岩藻糖果在TNBC细胞中的常规因子的表达,以及人脐血管内皮细胞(HUVEC)抑制肿瘤引发管形成。我们还观察到岩藻糖糖阻断肿瘤粘附和侵袭Huvecs。令人惊讶的是,Fucoinean鲁棒地抑制了Huvecs的管形成。此外,在转基因斑马鱼模型中抑制了岩藻糖膜和微转移和微转移。 L. Japonica Fucoinoidan在TNBC中的侵袭性和雌激素衰减表现出有效的抗肿瘤作用。 (c)2020 Elsevier B.v.保留所有权利。

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