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首页> 外文期刊>Oncology letters >A furin inhibitor downregulates osteosarcoma cell migration by downregulating the expression levels of MT1-MMP via the Wnt signaling pathway
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A furin inhibitor downregulates osteosarcoma cell migration by downregulating the expression levels of MT1-MMP via the Wnt signaling pathway

机译:弗林蛋白酶抑制剂通过Wnt信号通路通过下调MT1-MMP的表达水平来下调骨肉瘤细胞的迁移

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This study aimed to explore the exact mechanism of the effect of a furin inhibitor on the migration and invasion of MG-63 and Saos-2 osteosarcoma cells. MG-63 and Saos-2 osteosarcoma cells were treated with regular culture medium in the presence or absence of 480 nM α1-antitrypsin Portland (α1-PDX). Wound-healing and Transwell assays were used for the detection of the effects of α1-PDX on MG-63 and Saos-2 osteosarcoma cell migration and invasion. Western blot analysis and reverse transcription-polymerase chain reaction were performed to detect the expression levels of membrane type I matrix metalloproteinase (MT1-MMP), Wnt and β-catenin. A chromatin immunoprecipitation assay was used for detection of the levels of MT1-MMP gene transcription activity. The results showed that α1-PDX treatment significantly reduced the migration and invasion ability of the cells. Notably, the expression levels of MT1-MMP decreased evidently upon α1-PDX treatment, paralleled with reductions in the expression levels of Wnt and β-catenin. Further analysis of the transcriptional activity of MT1-MMP revealed that the α1-PDX-induced downregulation of the levels of MT1-MMP was mediated by the Wnt signaling pathway. These data suggest that α1-PDX plays a vital role in inhibiting MG-63 and Saos-2 osteosarcoma cell migration and invasion by downregulating the expression levels of MT1-MMP via the Wnt signaling pathway.
机译:这项研究旨在探讨弗林蛋白酶抑制剂对MG-63和Saos-2骨肉瘤细胞迁移和侵袭的确切机制。在有或没有480 nMα1-抗胰蛋白酶波特兰(α1-P​​DX)的情况下,用常规培养基处理MG-63和Saos-2骨肉瘤细胞。伤口愈合和Transwell分析用于检测α1-PDX对MG-63和Saos-2骨肉瘤细胞迁移和侵袭的影响。进行蛋白质印迹分析和逆转录聚合酶链反应以检测I型膜基质金属蛋白酶(MT1-MMP),Wnt和β-catenin的表达水平。染色质免疫沉淀法用于检测MT1-MMP基因转录活性的水平。结果表明,α1-PDX处理显着降低了细胞的迁移和侵袭能力。值得注意的是,MT1-MMP的表达水平在α1-PDX处理后明显降低,与Wnt和β-连环蛋白的表达水平降低平行。对MT1-MMP转录活性的进一步分析表明,α1-PDX诱导的MT1-MMP水平下调是由Wnt信号通路介导的。这些数据表明,α1-PDX通过下调经由Wnt信号通路的MT1-MMP的表达水平,在抑制MG-63和Saos-2骨肉瘤细胞的迁移和侵袭中起着至关重要的作用。

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