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癌症患者来源的微囊泡上的组织因子活性。

Tissue factor activity on microvesicles from cancer patients.

机构信息

Clinic for Hematology and Oncology, Section Experimental Oncology, University Hospital od Schleswig-Holstein, UKSH, Campus Luebeck, Ratzeburger Allee 160, 23528, Luebeck, Germany.

出版信息

J Cancer Res Clin Oncol. 2020 Feb;146(2):467-475. doi: 10.1007/s00432-019-03073-0. Epub 2019 Nov 16.

Abstract

PURPOSE

The expression of active tissue factor (TF) on the surface of microvesicles (MVs) is essential for the activation of the coagulation system and transduction of the signaling pathways in cancer cells. In its use as a biomarker for cancer-associated venous thromboembolism (VTE), TF has shown high expression variability. As a contribution to this discussion, we present a study investigating plasma samples from patients with various progressive tumors at high risk for VTE.

METHODS

Based on our previous study uncovering microvesicles (MVs), the larger ectosome-like extracellular vesicles (EV), as the major source of TF activity in EV preparations, we now determined TF activity on enriched MVs isolated from plasma of cancer patients and compared it with that on MVs from healthy individuals.

RESULTS

We found considerably higher amounts of MVs as well as higher levels of MV-bound TF activities in the plasma of cancer patients. We also show that preparations from plasma of cancer patients have the potency to induce ERK phosphorylation in a human tumor cell line through proteinase-activated receptor two (PAR2) activation.

CONCLUSION

We suggest that MVs instead of whole EV preparations, and TF activity rather than its antigenic quantification should be used in clinical studies for identifying patients with progressive tumors at high risk for VTE.

摘要

目的

细胞膜微囊泡(MVs)表面的组织因子(TF)表达对于激活凝血系统和传递癌细胞中的信号通路至关重要。在将 TF 作为癌症相关静脉血栓栓塞症(VTE)的生物标志物的应用中,已显示出其高表达变异性。作为对此讨论的贡献,我们进行了一项研究,调查了来自各种进展性肿瘤且有高 VTE 风险的患者的血浆样本。

方法

基于我们之前揭示微囊泡(MVs),即较大的类外泌体样细胞外囊泡(EV),是 EV 制剂中 TF 活性的主要来源的研究,我们现在确定了从癌症患者血浆中分离的富含 MVs 上的 TF 活性,并将其与健康个体的 MVs 上的活性进行了比较。

结果

我们发现癌症患者血浆中 MV 的数量以及 MV 结合的 TF 活性水平明显更高。我们还表明,来自癌症患者血浆的制剂通过蛋白水解酶激活受体 2(PAR2)的激活,具有在人肿瘤细胞系中诱导 ERK 磷酸化的能力。

结论

我们建议在临床研究中,应使用 MV 代替整个 EV 制剂,并且应使用 TF 活性而不是其抗原定量来识别有进展性肿瘤且有高 VTE 风险的患者。

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