Department of Pathology, Boston University Medical Campus, 670 Albany St., Room 510, Boston, MA 02118, USA.
Mol Cancer Ther. 2012 Mar;11(3):538-48. doi: 10.1158/1535-7163.MCT-11-0555. Epub 2012 Feb 21.
A strict physiological balance between endogenous proangiogenic and antiangiogenic factors controls endothelial cell functions, such that endothelial cell growth is normally restrained. However, in pathologic angiogenesis, a shift occurs in the balance of regulators, favoring endothelial growth. Much of the control of angiogenic events is instigated through hypoxia-induced VEGF expression. The ubiquitin-proteasome system (UPS) plays a central role in fine-tuning the functions of core proangiogenic proteins, including VEGF, VEGFR-2, angiogenic signaling proteins (e.g., the PLCγ1 and PI3 kinase/AKT pathways), and other non-VEGF angiogenic pathways. The emerging mechanisms by which ubiquitin modification of angiogenic proteins control angiogenesis involve both proteolytic and nonproteolytic functions. Here, I review recent advances that link the UPS to regulation of angiogenesis and highlight the potential therapeutic value of the UPS in angiogenesis-associated diseases.
严格的内源性促血管生成和抗血管生成因子之间的生理平衡控制着内皮细胞的功能,使内皮细胞的生长通常受到抑制。然而,在病理性血管生成中,调节因子的平衡发生了转变,有利于内皮细胞的生长。血管生成事件的大部分控制是通过缺氧诱导的 VEGF 表达引发的。泛素-蛋白酶体系统(UPS)在微调核心促血管生成蛋白的功能方面发挥着核心作用,包括 VEGF、VEGFR-2、血管生成信号蛋白(例如,PLCγ1 和 PI3 激酶/AKT 途径)和其他非 VEGF 血管生成途径。泛素修饰血管生成蛋白控制血管生成的新兴机制既涉及蛋白水解功能,也涉及非蛋白水解功能。在这里,我回顾了将 UPS 与血管生成调节联系起来的最新进展,并强调了 UPS 在与血管生成相关的疾病中的潜在治疗价值。