Clinical Division of Hematology and Hemostaseology, Department of Medicine I, Comprehensive Cancer Center Vienna, Medical University of Vienna, Austria.
Clinical Division of Hematology and Hemostaseology, Department of Medicine I, Comprehensive Cancer Center Vienna, Medical University of Vienna, Austria.
Thromb Res. 2018 Apr;164 Suppl 1:S34-S39. doi: 10.1016/j.thromres.2018.01.020.
Venous thromboembolism (VTE) is a frequent and life-threatening complication in patients with cancer. The underlying mechanisms of cancer-associated VTE are still not completely understood. However, emerging studies indicate that the mechanisms differ across tumor types. A recent study revealed that in patients with brain tumors, podoplanin overexpression is strongly correlated with intratumoral thrombotic vessels, hypercoagulability and increased VTE risk. In vitro experiments demonstrated that platelet aggregation induced by human glioblastoma cells was highly podoplanin-dependent. Podoplanin is a transmembrane glycoprotein with the ability to induce platelet activation via the platelet-receptor CLEC-2. Moreover, podoplanin is a lymphatic endothelial marker and exhibits substantial functions during embryonic development. It is variously upregulated by many cancers including primary brain tumors and linked to malignant progression and poor survival. In vivo studies have indicated that the podoplanin-CLEC-2 axis might be mechanistically involved in the development of venous thrombosis. In this review, we discuss the role of podoplanin in promoting cancer-associated VTE. Since podoplanin is associated with VTE risk in brain tumor patients, it could be a useful biomarker to identify patients at very high VTE risk. Those patients may benefit from primary thromboprophylaxis. In addition, the podoplanin-CLEC-2 axis might serve as an attractive target for new therapies against cancer-associated VTE.
静脉血栓栓塞症(VTE)是癌症患者常见且危及生命的并发症。癌症相关 VTE 的潜在机制尚不完全清楚。然而,新的研究表明,这些机制因肿瘤类型而异。最近的一项研究表明,在脑瘤患者中,足突蛋白的过表达与肿瘤内血栓性血管、高凝状态和 VTE 风险增加密切相关。体外实验表明,人胶质母细胞瘤细胞诱导的血小板聚集高度依赖于足突蛋白。足突蛋白是一种跨膜糖蛋白,通过血小板受体 CLEC-2 具有诱导血小板激活的能力。此外,足突蛋白是淋巴管内皮标志物,在胚胎发育过程中具有重要功能。许多癌症包括原发性脑肿瘤都会不同程度地上调足突蛋白,并与恶性进展和不良预后相关。体内研究表明,足突蛋白-CLEC-2 轴可能在静脉血栓形成的发展中具有机制作用。在这篇综述中,我们讨论了足突蛋白在促进癌症相关 VTE 中的作用。由于足突蛋白与脑肿瘤患者的 VTE 风险相关,它可能是识别 VTE 风险极高的患者的有用生物标志物。这些患者可能受益于一级预防性抗凝治疗。此外,足突蛋白-CLEC-2 轴可能成为针对癌症相关 VTE 的新治疗方法的有吸引力的靶点。