首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Inhibitory Effect of Alisma canaliculatum Ethanolic Extract on NF-κB-Dependent CXCR3 and CXCL10 Expression in TNFα-Exposed MDA-MB-231 Breast Cancer Cells
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Inhibitory Effect of Alisma canaliculatum Ethanolic Extract on NF-κB-Dependent CXCR3 and CXCL10 Expression in TNFα-Exposed MDA-MB-231 Breast Cancer Cells

机译:泽泻乙醇提取物对TNFα暴露的MDA-MB-231乳腺癌细胞中NF-κB依赖性CXCR3和CXCL10表达的抑制作用

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摘要

CXC motif chemokine ligand 10 (CXCL10) and its receptor CXC motif chemokine receptor 3 (CXCR3), play important roles in the motility of breast cancer cells. Alisma canaliculatum is a herb that has been used as a traditional medicine for thousands of years in Korea and China. Whether A. canaliculatum inhibits the motility of metastatic breast cancer cells is not clear yet. In this study, we show that A. canaliculatum ethanolic extract (ACE) prevented tumor necrosis factor-alpha (TNFα)-induced migration of MDA-MB-231 cells. ACE significantly attenuated TNFα-induced upregulation of CXCL10 and CXCR3 expression at the gene promoter level. Mechanistically, ACE inhibits TNFα-induced phosphorylation of inhibitor of κB (IκB) kinase (IKK), IκB and p65/RelA, leading to the suppression of nuclear translocation of p65/RelA nuclear factor kappa-B (NF-κB). Also, ACE inhibited NF-κB-dependent CXCR3 and CXCL10 promoter activities. These results suggest that ACE abrogates TNFα-induced migration of MDA-MB-231 breast cancer cells through down-regulation of IKK-NF-κB-dependent CXCR3 and CXCL10 expression. Our results suggest that ACE has potential as a herbal supplement for the inhibition of breast cancer metastasis.
机译:CXC基序趋化因子配体10(CXCL10)及其受体CXC基序趋化因子受体3(CXCR3)在乳腺癌细胞的运动中起重要作用。泽泻是在韩国和中国数千年来一直作为传统药物使用的草药。 Canaliculatum是否能抑制转移性乳腺癌细胞的活力尚不清楚。在这项研究中,我们表明,A。canaliculatum乙醇提取物(ACE)阻止了肿瘤坏死因子-α(TNFα)诱导的MDA-MB-231细胞迁移。 ACE在基因启动子水平上显着减弱了TNFα诱导的CXCL10和CXCR3表达的上调。从机理上讲,ACE抑制TNFα诱导的κB(IκB)激酶(IKK),IκB和p65 / RelA抑制剂的磷酸化,从而抑制p65 / RelA核因子kappa-B(NF-κB)的核易位。此外,ACE抑制NF-κB依赖性CXCR3和CXCL10启动子活性。这些结果表明,ACE通过下调IKK-NF-κB依赖性CXCR3和CXCL10表达来消除TNFα诱导的MDA-MB-231乳腺癌细胞迁移。我们的结果表明,ACE有潜力作为抑制乳腺癌转移的草药补充剂。

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