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Berberine Inhibits Metastasis of Nasopharyngeal Carcinoma 5-8F Cells by Targeting Rho Kinase-mediated Ezrin Phosphorylation at Threonine 567*

机译:小碱通过靶向苏氨酸567的Rho激酶介导的Ezrin磷酸化抑制鼻咽癌5-8F细胞转移*

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摘要

Ezrin is highly expressed in metastatic tumors and is involved in filopodia formation as well as promotion of tumor metastasis. Thus, Ezrin may serve as a potential target for anti-metastatic therapy. This study demonstrates that berberine reduces filopodia formation of a nasopharyngeal carcinoma (NPC) cell line, 5-8F, at non-cytotoxic concentrations. Furthermore, invasion and motility of 5-8F cells are decreased in a dose- and time-dependent manner, resulting in 73.0% invasion and 67.0% motility inhibition at 20 μm. The inhibitory effects of berberine on 5-8F cell metastasis were further confirmed in a mouse model of metastasis. Berberine treatment in vivo resulted in a 51.1% inhibition of tumor metastasis to the lymph nodes and decreased Ezrin phosphorylation at threonine 567 in metastatic samples. Berberine suppressed the presence of phosphorylated Ezrin (phospho-Ezrin) in a dose- and time-dependent manner but had no effect on total Ezrin protein expression at non-cytotoxic concentrations. Furthermore, the inhibitory effects of berberine on phospho-Ezrin were dependent on the suppression of Rho kinase activity. Reduction of Ezrin phosphorylation at Thr567 by berberine was associated with its inhibitory effect on filopodia formation in 5-8F cells. However, berberine did not effectively inhibit the motility and invasion of NPC cells containing Ezrin Thr567 mutants. These results confirm that berberine inhibits Ezrin phosphorylation at Thr567. Nonetheless, berberine reduces motility and invasion of cells and inhibits tumor metastasis. The reduction of Rho kinase-mediated Ezrin phosphorylation mediated by berberine may be a novel anti-metastatic pathway in NPC 5-8F cells.
机译:Ezrin在转移性肿瘤中高表达,并参与丝状伪足的形成以及肿瘤转移的促进。因此,埃兹林可作为抗转移疗法的潜在靶标。这项研究表明,小non碱在非细胞毒性浓度下可降低鼻咽癌(NPC)细胞系5-8F的丝足形成。此外,5-8F细胞的侵袭和运动以剂量和时间依赖的方式降低,导致在20μm处的侵袭率为73.0%,运动抑制率为67.0%。在转移的小鼠模型中进一步证实了小ber碱对5-8F细胞转移的抑制作用。在体内进行小碱治疗后,转移样品中的肿瘤转移至淋巴结的抑制率为51.1%,苏氨酸567处的Ezrin磷酸化降低。小ber碱以剂量和时间依赖性的方式抑制磷酸化Ezrin(phospho-Ezrin)的存在,但在非细胞毒性浓度下对总Ezrin蛋白表达没有影响。此外,小ber碱对磷酸化Ezrin的抑制作用取决于Rho激酶活性的抑制。小ber碱在Thr567处Ezrin磷酸化的减少与其对5-8F细胞丝状伪足形成的抑制作用有关。但是,小ber碱不能有效抑制含有Ezrin Thr567突变体的NPC细胞的运动性和侵袭性。这些结果证实小ber碱在Thr567处抑制Ezrin磷酸化。尽管如此,小ber碱可降低运动性和细胞侵袭并抑制肿瘤转移。小ber碱介导的Rho激酶介导的Ezrin磷酸化的减少可能是NPC 5-8F细胞中的新型抗转移途径。

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