Pugh Christopher W, Ratcliffe Peter J
The Henry Wellcome Building of Genomic Medicine, Roosevelt Drive, Oxford, OX3 7BN, UK.
Nat Med. 2003 Jun;9(6):677-84. doi: 10.1038/nm0603-677.
The regulation of angiogenesis by hypoxia is an important component of homeostatic mechanisms that link vascular oxygen supply to metabolic demand. Molecular characterization of angiogenic pathways, identification of hypoxia-inducible factor (HIF) as a key transcriptional regulator of these molecules, and the definition of the HIF hydoxylases as a family of dioxygenases that regulate HIF in accordance with oxygen availability have provided new insights into this process. Here we review these findings, and the role of HIF in developmental, adaptive and neoplastic angiogenesis. We also discuss the implications of oncogenic activation of extensive, physiologically interconnected hypoxia pathways for the tumor phenotype.
缺氧对血管生成的调节是一种稳态机制的重要组成部分,该机制将血管氧供应与代谢需求联系起来。血管生成途径的分子特征、缺氧诱导因子(HIF)作为这些分子的关键转录调节因子的鉴定,以及HIF羟化酶作为一类根据氧可用性调节HIF的双加氧酶家族的定义,为这一过程提供了新的见解。在此,我们综述这些发现以及HIF在发育、适应性和肿瘤血管生成中的作用。我们还讨论了广泛的、生理上相互关联的缺氧途径的致癌激活对肿瘤表型的影响。