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首页> 外文期刊>Cell death & disease. >Knockdown of MSI2 inhibits metastasis by interacting with caveolin-1 and inhibiting its ubiquitylation in human NF1-MPNST cells
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Knockdown of MSI2 inhibits metastasis by interacting with caveolin-1 and inhibiting its ubiquitylation in human NF1-MPNST cells

机译:MSI2的敲低通过与Caveolin-1相互作用来抑制转移,并抑制人NF1-MPNST细胞中的ubiquitylation

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Malignant peripheral nerve sheath tumours (MPNSTs) are highly aggressive Schwann cell-derived sarcomas, and they are either associated with neurofibromatosis type 1 (NF1) or sporadic. Our previous study found that high mobility group protein A2 (HMGA2) regulates NF1-MPNST growth through Musashi-2 (MSI2); however, whether MSI2 regulates MPNST metastasis and what the mechanism is remain unclear. Here, we demonstrated that the protein caveolin-1 (CAV1) directly interacts with MSI2 in human NF1-MPNST cells. Moreover, we discovered that knockdown of MSI2 induces CAV1 protein expression by inhibiting its ubiquitylation level in NF1-MPNSTs. In addition, CAV1 mediates the suppressive function of MSI2 in epithelial-mesenchymal transition, migration and invasion in vitro and metastasis in vivo. These results help to reveal the potential mechanisms of MSI2 as a target of antimetastatic treatment for human NF1-MPNST.
机译:恶性周围神经鞘瘤(MPNSTS)是高度侵略性的施旺细胞衍生的肉瘤,它们与神经纤维素病1(NF1)或散发有关。我们以前的研究发现,高迁移率组蛋白A2(HMGA2)通过Musashi-2(MSI2)调节NF1-MPNST生长;但是,MSI2是否调节MPNST转移以及机制仍不清楚的是什么。在这里,我们证明蛋白质caveolin-1(Cav1)在人NF1-MPNST细胞中直接与MSI2相互作用。此外,我们发现MSI2的敲低通过抑制其NF1-MPNSTS中的泛醌水平来诱导CAV1蛋白表达。此外,Cav1介导MSI2在体外上皮 - 间充质转换,迁移和侵袭中的抑制函数。这些结果有助于揭示MSI2作为人NF1-MPNST抗常用治疗目标的潜在机制。

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