Vascular Program, Institute for Cell Engineering; Departments of Pediatrics, Medicine, Oncology, Radiation Oncology, and Biological Chemistry; and McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205; email:
Annu Rev Pathol. 2014;9:47-71. doi: 10.1146/annurev-pathol-012513-104720. Epub 2013 Aug 7.
Hypoxia-inducible factors (HIFs) are transcriptional activators that function as master regulators of oxygen homeostasis, which is disrupted in disorders affecting the circulatory system and in cancer. The role of HIFs in these diseases has been elucidated by clinical studies and by analyses of mouse models. HIFs play a protective role in the pathophysiology of myocardial ischemia due to coronary artery disease, limb ischemia due to peripheral arterial disease, pressure-overload heart failure, wound healing, and chronic rejection of organ transplants. In contrast, HIFs contribute to the pathogenesis of pulmonary arterial hypertension, systemic hypertension associated with sleep apnea, ocular neovascularization, hereditary erythrocytosis, and cancer.
缺氧诱导因子 (HIFs) 是转录激活因子,作为氧平衡的主调控因子发挥作用,而氧平衡在影响循环系统和癌症的疾病中会被打破。HIFs 在这些疾病中的作用已通过临床研究和对小鼠模型的分析得到阐明。HIFs 在由于冠状动脉疾病引起的心肌缺血、由于外周动脉疾病引起的肢体缺血、压力超负荷性心力衰竭、伤口愈合和器官移植的慢性排斥等病理生理学中发挥保护作用。相比之下,HIFs 导致肺动脉高压、与睡眠呼吸暂停相关的系统性高血压、眼新生血管形成、遗传性红细胞增多症和癌症的发病机制。