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癌症中的组织因子与蛋白酶激活受体信号传导

Tissue factor and protease-activated receptor signaling in cancer.

作者信息

Schaffner Florence, Ruf Wolfram

机构信息

Research Associate, Department of Immunology, The Scripps Research Institute, La Jolla, California, USA.

出版信息

Semin Thromb Hemost. 2008 Mar;34(2):147-53. doi: 10.1055/s-2008-1079254.

Abstract

The activation of the coagulation cascade in the tumor microenvironment is a key feature of advanced malignancies. On tumor cells, tissue factor (TF) plays a central role to initiate cross-talk through the release of procoagulant microparticles or through direct, protease-activated receptor (PAR)-mediated cell signaling that leads to the production of soluble cytokines and angiogenic growth factors. In addition, the hemostatic system in the host compartment sustains crucial circuits that promote metastasis and support tumor growth and angiogenesis. Experimental tumor and genetic models have defined specific pathways that are supported by tumor cell and host TF and have identified potential therapeutic modalities to specifically interrupt TF signaling in tumor biology without impairment of hemostatic functions.

摘要

肿瘤微环境中凝血级联反应的激活是晚期恶性肿瘤的一个关键特征。在肿瘤细胞上,组织因子(TF)通过释放促凝微粒或通过直接的蛋白酶激活受体(PAR)介导的细胞信号传导发挥核心作用,引发相互作用,导致可溶性细胞因子和血管生成生长因子的产生。此外,宿主区室中的止血系统维持着促进转移、支持肿瘤生长和血管生成的关键通路。实验性肿瘤和遗传模型已经确定了由肿瘤细胞和宿主TF支持的特定途径,并确定了在不损害止血功能的情况下特异性中断肿瘤生物学中TF信号传导的潜在治疗方式。

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