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TIAM1 Antagonizes TAZ/YAP Both in the Destruction Complex in the Cytoplasm and in the Nucleus to Inhibit Invasion of Intestinal Epithelial Cells.TIAM1在细胞质中的破坏复合体以及细胞核中均拮抗TAZ/YAP,以抑制肠上皮细胞的侵袭。
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Identification of cancer-associated missense mutations in hace1 that impair cell growth control and Rac1 ubiquitylation.鉴定 hace1 中的致癌错义突变,这些突变会损害细胞生长控制和 Rac1 的泛素化。
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Nuclear PKCι-ECT2-Rac1 and Ribosome Biogenesis: A Novel Axis in Lung Tumorigenesis.核 PKCι-ECT2-Rac1 和核糖体生物发生:肺癌发生中的新轴。
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Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal Interactions with Oncogenic Ras.基因必需性分析揭示基因网络以及与致癌性Ras的合成致死相互作用。
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癌症中的Rac GTP酶:从旧概念到新范式

The Rac GTPase in Cancer: From Old Concepts to New Paradigms.

作者信息

Kazanietz Marcelo G, Caloca Maria J

机构信息

Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Instituto de Biología y Genética Molecular, Consejo Superior de Investigaciones Científicas, Universidad de Valladolid, Valladolid, Spain.

出版信息

Cancer Res. 2017 Oct 15;77(20):5445-5451. doi: 10.1158/0008-5472.CAN-17-1456. Epub 2017 Aug 14.

DOI:10.1158/0008-5472.CAN-17-1456
PMID:28807941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5645227/
Abstract

Rho family GTPases are critical regulators of cellular functions that play important roles in cancer progression. Aberrant activity of Rho small G-proteins, particularly Rac1 and their regulators, is a hallmark of cancer and contributes to the tumorigenic and metastatic phenotypes of cancer cells. This review examines the multiple mechanisms leading to Rac1 hyperactivation, particularly focusing on emerging paradigms that involve gain-of-function mutations in Rac and guanine nucleotide exchange factors, defects in Rac1 degradation, and mislocalization of Rac signaling components. The unexpected pro-oncogenic functions of Rac GTPase-activating proteins also challenged the dogma that these negative Rac regulators solely act as tumor suppressors. The potential contribution of Rac hyperactivation to resistance to anticancer agents, including targeted therapies, as well as to the suppression of antitumor immune response, highlights the critical need to develop therapeutic strategies to target the Rac pathway in a clinical setting. .

摘要

Rho家族GTP酶是细胞功能的关键调节因子,在癌症进展中发挥重要作用。Rho小G蛋白,特别是Rac1及其调节因子的异常活性是癌症的一个标志,并促成癌细胞的致瘤和转移表型。本综述探讨了导致Rac1过度激活的多种机制,特别关注涉及Rac和鸟嘌呤核苷酸交换因子功能获得性突变、Rac1降解缺陷以及Rac信号成分错误定位的新范式。Rac GTP酶激活蛋白意外的促癌功能也挑战了这些负性Rac调节因子仅作为肿瘤抑制因子的传统观念。Rac过度激活对包括靶向治疗在内的抗癌药物耐药性以及对抗肿瘤免疫反应抑制的潜在影响,凸显了在临床环境中开发靶向Rac途径治疗策略的迫切需求。