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首页> 外文期刊>Journal of Bone Oncology >von Willebrand factor promotes platelet-induced metastasis of osteosarcoma through activation of the VWF-GPIb axis
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von Willebrand factor promotes platelet-induced metastasis of osteosarcoma through activation of the VWF-GPIb axis

机译:von Willebrand因子通过激活VWF-GPIB轴来促进血小板诱导的骨肉瘤转移

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von Willebrand factor (VWF) is exclusively expressed in endothelial cells (ECs) and megakaryocytes, which plays a crucial role in the initiation of arterial thrombosis. Recent studies have shown that VWF is also expressed in osteosarcoma (OS) cells and participates in adhesion of cancer cells to platelets, thus promoting metastasis of OS cells. However, it is unclear how OS cell-derived VWF-platelet interaction contributes to the metastasis of OS. We hypothesized that the interaction is mediated by the binding between VWF A1 and GPIbα of platelets, a molecular mechanism similar to that of thrombosis. The increased expression of VWF in SAOS2 cells may contribute to the enhancement of platelet adhesion through the VWF-GPIb pathway, which could promote the migration and invasion capacities of SAOS2 cells in vitro. Antibodies that block the pathway could significantly inhibit the platelet-induced metastasis of OS cells. Our results suggest a theoretical basis for the development of new anti-OS metastasis drugs, and further enrich the mechanism of OS metastasis.
机译:Von Willebrand因子(VWF)仅在内皮细胞(ECS)和巨核细胞中表达,这在动脉血栓形成的开始中起着至关重要的作用。最近的研究表明,VWF也在骨肉瘤(OS)细胞中表达,并参与癌细胞对血小板的粘附,从而促进OS细胞的转移。然而,目前尚不清楚OS细胞衍生的VWF-血小板相互作用如何促成OS的转移。我们假设相互作用是通过血小板VWF A1和GPIBα之间的结合介导的,该分子机制类似于血栓形成。 VWF在SAOS2细胞中的表达增加可能导致通过VWF-GPIB途径的血小板粘附,这可以促进SAOS2细胞在体外的迁移和侵袭能力。阻断途径的抗体可以显着抑制OS细胞的血小板诱导的转移。我们的结果表明了新的抗OS转移药物的发展的理论依据,并进一步丰富了OS转移的机制。

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