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蛋白酶激活受体、细胞凋亡与肿瘤生长。

Protease-activated receptors, apoptosis and tumor growth.

作者信息

Borensztajn Keren S, Spek C Arnold

机构信息

Center for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Pathophysiol Haemost Thromb. 2008;36(3-4):137-47. doi: 10.1159/000175152. Epub 2009 Jan 27.

Abstract

Protease-activated receptors (PARs) are G-protein-coupled receptors (GPCRs) that are activated by a unique proteolytic mechanism. Besides the important role of blood coagulation factors in preventing bleeding after vascular injury, these serine proteinases actively engage target cells thereby fulfilling critical functions in cell biology. Cellular responses triggered by coagulation factor-induced PAR activation suggest that PARs play an important role in proliferation, survival and/or malignant transformation of tumor cells. Indeed, PAR expression correlates with cancer malignancy and clinical studies show that anticoagulant treatment is beneficial in cancer patients. In this review, we provide an overview on the PAR family, their mode of activation and mechanisms by which PAR signaling is terminated. In addition, we discuss the relationship between blood coagulation and cancer biology focusing on the potential role of PAR-induced modulation of cell survival, apoptosis and tumor growth.

摘要

蛋白酶激活受体(PARs)是通过独特的蛋白水解机制激活的G蛋白偶联受体(GPCRs)。除了凝血因子在预防血管损伤后出血中的重要作用外,这些丝氨酸蛋白酶还积极作用于靶细胞,从而在细胞生物学中发挥关键功能。凝血因子诱导的PAR激活引发的细胞反应表明,PARs在肿瘤细胞的增殖、存活和/或恶性转化中起重要作用。事实上,PAR表达与癌症恶性程度相关,临床研究表明抗凝治疗对癌症患者有益。在本综述中,我们概述了PAR家族、它们的激活模式以及PAR信号终止的机制。此外,我们讨论了凝血与癌症生物学之间的关系,重点关注PAR诱导的细胞存活、凋亡和肿瘤生长调节的潜在作用。

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