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在血管生成过程中对血管内皮生长因子(VEGF)基因表达有影响的转录因子。

Transcription factors having impact on vascular endothelial growth factor (VEGF) gene expression in angiogenesis.

作者信息

Jośko Jadwiga, Mazurek Michał

机构信息

Department of Environmental Medicine and Epidemiology, Medical University of Silesia, Zabrze-Rokitnica, Poland.

出版信息

Med Sci Monit. 2004 Apr;10(4):RA89-98.

Abstract

This article discusses the role of transcription factors in vascular endothelial growth factor (VEGF) gene expression. Angiogenesis is a complex and multilevel process of new capillary formation on the basis of already existing blood vessels. Physiologically, it is a very strictly regulated process, which results in a balance between stimulatory (angiogenic) and inhibitory (angiostatic) factors to control the correct development of blood vessels. There are many very well characterized angiogenic and angiostatic factors that can modulate VEGF expression. Some of them (e.g. HIF-1, AP-1, and Sp-1) are transcription factors, proteins that bind to the VEGF promoter to initiate and activate the transcription of a gene directly. Others, like nitric oxide or cytokines, are agents that stimulate the transcription factors through different cellular signaling pathways. There are also oncogenes (V-SRC, bcl-2) and tumor suppressor genes (VHL), the mutations of which lead indirectly to increased transcription of the VEGF gene.

摘要

本文讨论了转录因子在血管内皮生长因子(VEGF)基因表达中的作用。血管生成是在已有血管基础上形成新毛细血管的复杂多水平过程。生理上,这是一个受到严格调控的过程,其结果是刺激(促血管生成)和抑制(血管生成抑制)因子之间达到平衡,以控制血管的正常发育。有许多特征明确的促血管生成和血管生成抑制因子可调节VEGF表达。其中一些(如HIF-1、AP-1和Sp-1)是转录因子,即直接与VEGF启动子结合以启动和激活基因转录的蛋白质。其他因子,如一氧化氮或细胞因子,则是通过不同细胞信号通路刺激转录因子的物质。此外还有癌基因(V-SRC、bcl-2)和肿瘤抑制基因(VHL),它们的突变会间接导致VEGF基因转录增加。

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