Wang Q, Liu W, Fan J, Guo J, Shen F, Ma Z, Ruan C, Guo L, Jiang M, Zhao Y
Jiangsu Institute of Hematology, Key Laboratory of Thrombosis & Hemostasis of Ministry of Health, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Pathology Department, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
J Bone Oncol. 2020 Oct 8;25:100325. doi: 10.1016/j.jbo.2020.100325. eCollection 2020 Dec.
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.
血管性血友病因子(VWF)仅在内皮细胞(ECs)和巨核细胞中表达,在动脉血栓形成的起始过程中起关键作用。最近的研究表明,VWF也在骨肉瘤(OS)细胞中表达,并参与癌细胞与血小板的黏附,从而促进OS细胞的转移。然而,尚不清楚OS细胞衍生的VWF-血小板相互作用如何促进OS的转移。我们假设这种相互作用是由VWF A1与血小板的糖蛋白Ibα(GPIbα)之间的结合介导的,这是一种类似于血栓形成的分子机制。SAOS2细胞中VWF表达的增加可能通过VWF-GPIb途径促进血小板黏附增强,这可能促进SAOS2细胞在体外的迁移和侵袭能力。阻断该途径的抗体可显著抑制血小板诱导的OS细胞转移。我们的结果为开发新的抗OS转移药物提供了理论基础,并进一步丰富了OS转移的机制。