Meneses Ana M, Wielockx Ben
Heisenberg Research Group, Department of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, Technische Universität Dresden, Dresden, Germany.
Hypoxia (Auckl). 2016 Apr 11;4:53-67. doi: 10.2147/HP.S53576. eCollection 2016.
Oxygen represents one of the major molecules required for the development and maintenance of life. An adequate response to hypoxia is therefore required for the functioning of the majority of living organisms and relies on the activation of the hypoxia-inducible factor (HIF) pathway. HIF prolyl hydroxylase domain-2 (PHD2) has long been recognized as the major regulator of this response, controlling a myriad of outcomes that range from cell death to proliferation. However, this enzyme has been associated with more pathways, making the role of this protein remarkably complex under distinct pathologies. While a protective role seems to exist in physiological conditions such as erythropoiesis; the picture is more complex during pathologies such as cancer. Since the regulation of this enzyme and its closest family members is currently considered as a possible therapy for various diseases, understanding the different particular roles of this protein is essential.
氧气是生命发育和维持所需的主要分子之一。因此,大多数生物的正常功能需要对缺氧做出适当反应,这依赖于缺氧诱导因子(HIF)途径的激活。HIF脯氨酰羟化酶结构域2(PHD2)长期以来一直被认为是这种反应的主要调节因子,控制着从细胞死亡到增殖等无数结果。然而,这种酶与更多途径相关联,使得该蛋白在不同病理状态下的作用极为复杂。虽然在诸如红细胞生成等生理条件下似乎存在保护作用;但在癌症等病理状态下情况更为复杂。由于目前认为对这种酶及其最密切的家族成员的调节可能是治疗各种疾病的一种方法,了解该蛋白的不同特殊作用至关重要。