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鸟嘌呤核苷酸交换因子 Tiam1:细胞信号转导中的双面分子。

The guanine nucleotide exchange factor Tiam1: a Janus-faced molecule in cellular signaling.

机构信息

Department of Nephrology, Hypertension and Clinical Pharmacology, Department of Clinical Research, Inselspital, University of Bern, Switzerland.

Department of Nephrology, Hypertension and Clinical Pharmacology, Department of Clinical Research, Inselspital, University of Bern, Switzerland.

出版信息

Cell Signal. 2014 Mar;26(3):483-91. doi: 10.1016/j.cellsig.2013.11.034. Epub 2013 Dec 2.

Abstract

The Rho family of GTPases consists of several small proteins that have been described as molecular switches, playing important roles in a wide variety of fundamental cellular processes and in human diseases such as cancer. These proteins, active in the GTP conformation and inactive in the GDP form, are in turn regulated by guanine nucleotide exchange factors (GEFs), guanine nucleotide activating proteins (GAPs) and guanine dissociation inhibitors (GDIs). Two decades ago, Tiam1 (T-lymphoma invasion and metastasis) was identified as a GEF specific for Rac1 activation, but also for Cdc42 and in a lesser extent RhoA. Acting principally upstream of Rac1, Tiam1 is mainly involved in the regulation of Rac1 mediated signaling pathways including cytoskeletal activities, cell polarity, endocytosis and membrane trafficking, cell migration, adhesion and invasion, cell growth and survival, metastasis and carcinogenesis. However, given the large number of protein interaction domains found in its structure, it is possible that Tiam1 affects cellular processes in another way than through its GEF activity by interactions with other signaling proteins. Due to its functional diversity, Tiam1 is involved in multiple steps of tumorigenesis. As its name suggests, Tiam1 has been shown to increase T-cell lymphoma invasion and metastasis. It also promotes migration of fibroblasts, neuronal and cancer cells. On the contrary, Tiam1-induced cell adhesion has also been described, as opposed to cell migration. Moreover, studies indicate that Tiam1 is involved in both anti-apoptotic and pro-apoptotic mechanisms. While increasing evidence has demonstrated Tiam1's contribution to tumorigenesis and metastasis, others suggest that Tiam1 could have anti-cancer properties. In the present review, we discuss the current knowledge about the controversial roles of Tiam1 in cellular signaling. In particular, we will focus on Tiam1's regulation, its biological functions and implication in cancer.

摘要

Rho 家族的 GTPases 由几种小蛋白组成,这些小蛋白被描述为分子开关,在广泛的基本细胞过程和人类疾病(如癌症)中发挥着重要作用。这些蛋白在 GTP 构象中活跃,在 GDP 形式中不活跃,反过来又受到鸟嘌呤核苷酸交换因子 (GEF)、鸟嘌呤核苷酸激活蛋白 (GAP) 和鸟嘌呤解离抑制剂 (GDI) 的调节。二十年前,Tiam1(T 淋巴细胞浸润和转移)被鉴定为 Rac1 激活的特异性 GEF,但也可以激活 Cdc42,程度较低时也可以激活 RhoA。作为 Rac1 的主要上游调节剂,Tiam1 主要参与 Rac1 介导的信号通路的调节,包括细胞骨架活动、细胞极性、内吞作用和膜运输、细胞迁移、黏附和侵袭、细胞生长和存活、转移和癌变。然而,鉴于其结构中发现的大量蛋白质相互作用结构域,Tiam1 可能通过与其他信号蛋白的相互作用,以不同于其 GEF 活性的方式影响细胞过程。由于其功能多样性,Tiam1 参与了肿瘤发生的多个步骤。顾名思义,Tiam1 已被证明可增加 T 细胞淋巴瘤的浸润和转移。它还促进成纤维细胞、神经元和癌细胞的迁移。相反,也描述了 Tiam1 诱导的细胞黏附,而不是细胞迁移。此外,研究表明 Tiam1 参与了抗细胞凋亡和促细胞凋亡机制。虽然越来越多的证据表明 Tiam1 参与了肿瘤发生和转移,但其他人认为 Tiam1 可能具有抗癌特性。在本综述中,我们讨论了当前关于 Tiam1 在细胞信号转导中争议角色的知识。特别是,我们将重点讨论 Tiam1 的调节、生物学功能及其在癌症中的意义。

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