Goh Chia Yin, Patmore Sean, Smolenski Albert, Howard Jane, Evans Shane, O'Sullivan Jamie, McCann Amanda
UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin, Dublin 4, Ireland; UCD School of Medicine, College of Health and Agricultural Sciences (CHAS), University College Dublin, Belfield, Dublin, Dublin 4, Ireland.
Irish Centre for Vascular Biology, School of Pharmacy and Biomolecular Sciences, Royal College of Surgeons in Ireland, Dublin, Dublin 2, Ireland.
Transl Oncol. 2021 Apr;14(4):101033. doi: 10.1016/j.tranon.2021.101033. Epub 2021 Feb 8.
Breast cancer is the most common female cancer globally, with approximately 12% of patients eventually developing metastatic disease. Critically, limited effective treatment options exist for metastatic breast cancer. Recently, von Willebrand factor (VWF), a haemostatic plasma glycoprotein, has been shown to play an important role in tumour progression and metastasis. In breast cancer, a significant rise in the plasma levels of VWF has been reported in patients with malignant disease compared to benign conditions and healthy controls, with an even greater increase seen in patients with disseminated disease. Direct interactions between VWF, tumour cells, platelets and endothelial cells may promote haematogenous dissemination and thus the formation of metastatic foci. Intriguingly, patients with metastatic disease have unusually large VWF multimers. This observation has been proposed to be a result of a dysfunctional or deficiency of VWF-cleaving protease activity, ADAMTS-13 activity, which may then regulate the platelet-tumour adhesive interactions in the metastatic process. In this review, we provide an overview of VWF in orchestrating the pathological process of breast cancer dissemination, and provide supporting evidence of the role of VWF in mediating metastatic breast cancer.
乳腺癌是全球最常见的女性癌症,约12%的患者最终会发展为转移性疾病。关键的是,转移性乳腺癌的有效治疗选择有限。最近,血管性血友病因子(VWF),一种血浆止血糖蛋白,已被证明在肿瘤进展和转移中起重要作用。在乳腺癌中,与良性疾病患者和健康对照相比,恶性疾病患者的血浆VWF水平显著升高,在播散性疾病患者中升高更为明显。VWF、肿瘤细胞、血小板和内皮细胞之间的直接相互作用可能促进血行播散,从而形成转移灶。有趣的是,转移性疾病患者有异常大的VWF多聚体。这一观察结果被认为是VWF裂解蛋白酶活性(ADAMTS-13活性)功能失调或缺乏的结果,而ADAMTS-13活性可能在转移过程中调节血小板与肿瘤的粘附相互作用。在这篇综述中,我们概述了VWF在协调乳腺癌播散的病理过程中的作用,并提供了VWF在介导转移性乳腺癌中作用的支持证据。