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IGF-1 increases laminin, cyclin D1, and p21Cip1 expression in glomerular mesangial cells: an investigation of the intracellular signaling pathway and cell-cycle progression.胰岛素样生长因子-1增加肾小球系膜细胞中层粘连蛋白、细胞周期蛋白D1和p21Cip1的表达:细胞内信号通路和细胞周期进程的研究
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Distinct roles of Akt1 and Akt2 in regulating cell migration and epithelial-mesenchymal transition.Akt1和Akt2在调节细胞迁移和上皮-间质转化中的不同作用。
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Effects of chronic Akt activation on glucose uptake in the heart.慢性Akt激活对心脏葡萄糖摄取的影响。
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Akt blocks breast cancer cell motility and invasion through the transcription factor NFAT.蛋白激酶B通过转录因子活化T细胞核因子阻断乳腺癌细胞的运动和侵袭。
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Hypoxia-induced HIF-1 alpha accumulation is augmented in a co-culture of keloid fibroblasts and human mast cells: involvement of ERK1/2 and PI-3K/Akt.缺氧诱导的HIF-1α积累在瘢痕疙瘩成纤维细胞与人类肥大细胞的共培养中增强:ERK1/2和PI-3K/Akt的参与
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Gab1, SHP2, and protein kinase A are crucial for the activation of the endothelial NO synthase by fluid shear stress.Gab1、SHP2和蛋白激酶A对于流体切应力激活内皮型一氧化氮合酶至关重要。
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Rho, Rac, Pak and angiogenesis: old roles and newly identified responsibilities in endothelial cells.Rho、Rac、Pak与血管生成:内皮细胞中的旧有作用及新发现的职责
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内皮细胞中的Akt1与血管生成

Akt1 in endothelial cell and angiogenesis.

作者信息

Somanath Payaningal R, Razorenova Olga V, Chen Juhua, Byzova Tatiana V

机构信息

Department of Molecular Cardiology, Joseph J. Jacobs Center for Thrombosis and Vascular Biology, Taussig Cancer Center, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.

出版信息

Cell Cycle. 2006 Mar;5(5):512-8. doi: 10.4161/cc.5.5.2538. Epub 2006 Mar 1.

DOI:10.4161/cc.5.5.2538
PMID:16552185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1569947/
Abstract

Akt, also known as Protein kinase B (PKB), regulates essential cellular functions such as migration, proliferation, differentiation, apoptosis, and metabolism. Akt influences the expression and/or activity of various pro- and anti-angiogenic factors and Akt isoforms (Akt1, Akt2 and Akt3) have been proposed as therapeutic targets for angiogenesis-related anomalies such as cancer and ischemic injury.

摘要

Akt,也称为蛋白激酶B(PKB),可调节细胞的基本功能,如迁移、增殖、分化、凋亡和代谢。Akt会影响多种促血管生成和抗血管生成因子的表达和/或活性,并且Akt亚型(Akt1、Akt2和Akt3)已被提议作为针对癌症和缺血性损伤等血管生成相关异常的治疗靶点。