首页> 外文期刊>Oncology letters >Hispolon inhibits TPA-induced invasion by reducing MMP-9 expression through the NF-B signaling pathway in MDA-MB-231 human breast cancer cells
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Hispolon inhibits TPA-induced invasion by reducing MMP-9 expression through the NF-B signaling pathway in MDA-MB-231 human breast cancer cells

机译:Hispolon通过降低MDA-MB-231人乳腺癌细胞中NF-B信号通路的MMP-9表达来抑制TPA诱导的侵袭

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Hispolon has been demonstrated to possess analgesic, anti-inflammatory and anticancer activities. However, whether hispolon prevents the invasion of breast carcinoma cells and the underlying mechanisms of its action remain unknown. In the present study, various assays, including a matrigel-based Transwell invasion assay and electrophoretic mobility shift assay, were used to investigate the anti-invasion effect of hispolon and explore its mechanism of action. The results revealed that hispolon inhibited the 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced migration and invasion of MDA-MB-231 human breast cancer cells at non-toxic concentrations. Hispolon also prevented the TPA-induced secretion of matrix metalloproteinase-9 (MMP-9) and reduced its expression at the transcriptional and translational levels. Furthermore, the phosphorylation of IB was reduced by hispolon, which resulted in the suppression of nuclear factor-B (NF-B), and p65 phosphorylation and nuclear translocation. An electrophoretic mobility shift assay demonstrated that NF-B DNA-binding activity was induced by TPA and inhibited by hispolon. In addition, Bay 11-7082, which is a specific inhibitor of NF-B, functioned in a similar manner as hispolon and blocked the secretion and expression of MMP-9. In conclusion, the results of the present study indicated that hispolon inhibited TPA-induced migration and invasion of MDA-MB-231 cells by reducing the secretion and expression of MMP-9 through the NF-B signaling pathway.
机译:已证明Hispolon具有止痛,抗炎和抗癌活性。但是,组蛋白是否能阻止乳腺癌细胞的侵袭及其作用的潜在机制仍然未知。在本研究中,包括基于基质胶的Transwell入侵分析和电泳迁移率迁移分析在内的各种分析方法均用于研究组蛋白的抗侵袭作用并探讨其作用机理。结果显示,组蛋白以无毒浓度抑制了12-O-十四烷酰佛波醇13-乙酸盐(TPA)诱导的MDA-MB-231人乳腺癌细胞迁移和侵袭。 Hispolon还可以防止TPA诱导的基质金属蛋白酶9(MMP-9)分泌,并在转录和翻译水平上降低其表达。此外,组蛋白降低了IB的磷酸化,从而抑制了核因子B(NF-B),p65的磷酸化和核易位。电泳迁移率变动分析表明,TPA诱导NF-B DNA结合活性,而组蛋白抑制NF-B DNA结合活性。另外,Bay 11-7082是一种NF-B的特异性抑制剂,其功能类似于组蛋白,并阻止MMP-9的分泌和表达。总之,本研究的结果表明,组蛋白通过减少NF-B信号通路的MMP-9分泌和表达来抑制TPA诱导的MDA-MB-231细胞迁移和侵袭。

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