Colonne Chanukya K, Favaloro Emmanuel J, Pasalic Leonardo
Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), NSW Health Pathology, Westmead Hospital, Sydney, NSW 2145, Australia.
Sydney Centres for Thrombosis and Haemostasis, Sydney, NSW 2145, Australia.
Healthcare (Basel). 2022 Mar 16;10(3):557. doi: 10.3390/healthcare10030557.
von Willebrand factor (VWF) is a complex and large protein that is cleaved by ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin type 1 motif, member 13), and together they serve important roles in normal hemostasis. Malignancy can result in both a deficiency or excess of VWF, leading to aberrant hemostasis with either increased bleeding or thrombotic complications, as respectively seen with acquired von Willebrand syndrome and cancer-associated venous thromboembolism. There is emerging evidence to suggest VWF also plays a role in inflammation, angiogenesis and tumor biology, and it is likely that VWF promotes tumor metastasis. High VWF levels have been documented in a number of malignancies and in some cases correlate with more advanced disease and poor prognosis. Tumor cells can induce endothelial cells to release VWF and certain tumor cells have the capacity for de novo expression of VWF, leading to a proinflammatory microenvironment that is likely conducive to tumor progression, metastasis and micro-thrombosis. VWF can facilitate tumor cell adhesion to endothelial cells and aids with the recruitment of platelets into the tumor microenvironment, where tumor/platelet aggregates are able to form and facilitate hematogenous spread of cancer. As ADAMTS13 moderates VWF level and activity, it too is potentially involved in the pathophysiology of these events. VWF and ADAMTS13 have been explored as tumor biomarkers for the detection and prognostication of certain malignancies; however, the results are underdeveloped and so currently not utilized for clinical use. Further studies addressing the basic science mechanisms and real word epidemiology are required to better appreciate the intriguing connections between VWF, ADAMTS13 and malignancy. A better understanding of the role VWF and ADAMTS13 play in the promotion and inhibition of cancer and its metastasis will help direct further translational studies to aid with the development of novel cancer prognostic tools and treatment modalities.
血管性血友病因子(VWF)是一种复杂的大分子蛋白质,可被ADAMTS13(含血小板反应蛋白基序的解聚素和金属蛋白酶13)裂解,它们共同在正常止血过程中发挥重要作用。恶性肿瘤可导致VWF缺乏或过量,分别引起异常止血,出现出血增加或血栓形成并发症,如获得性血管性血友病综合征和癌症相关静脉血栓栓塞症。越来越多的证据表明,VWF在炎症、血管生成和肿瘤生物学中也发挥作用,并且VWF可能促进肿瘤转移。许多恶性肿瘤中都有VWF水平升高的记录,在某些情况下,这与疾病进展更严重和预后不良相关。肿瘤细胞可诱导内皮细胞释放VWF,某些肿瘤细胞具有VWF从头表达的能力,从而导致促炎微环境,这可能有利于肿瘤进展、转移和微血栓形成。VWF可促进肿瘤细胞与内皮细胞的黏附,并有助于将血小板募集到肿瘤微环境中,在那里肿瘤/血小板聚集体能够形成并促进癌症的血行转移。由于ADAMTS13可调节VWF水平和活性,它也可能参与这些事件的病理生理学过程。VWF和ADAMTS13已被探索作为某些恶性肿瘤检测和预后评估的肿瘤生物标志物;然而,相关结果尚不完善,目前未用于临床。需要进一步开展针对基础科学机制和实际流行病学的研究,以更好地理解VWF、ADAMTS13与恶性肿瘤之间的有趣联系。更好地了解VWF和ADAMTS13在促进和抑制癌症及其转移中的作用,将有助于指导进一步的转化研究,以辅助开发新型癌症预后工具和治疗方法。