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Diabetic atherosclerosis: is there a role for the hypoxia-inducible factors?
Author(s) -
Daniela Pirri,
Maria Fragiadaki,
Paul C. Evans
Publication year - 2020
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20200026
Subject(s) - diabetes mellitus , metabolic syndrome , insulin resistance , endothelial dysfunction , medicine , disease , hypoxia (environmental) , transcription factor , inflammation , obesity , bioinformatics , regulator , risk factor , endocrinology , biology , chemistry , genetics , gene , organic chemistry , oxygen
Atherosclerosis is a major cause of mortality worldwide and is driven by multiple risk factors, including diabetes. Diabetes is associated with either an insulin deficiency in its juvenile form or with insulin resistance and obesity in Type 2 diabetes mellitus, and the latter is clustered with other comorbidities to define the metabolic syndrome. Diabetes and metabolic syndrome are complex pathologies and are associated with cardiovascular risk via vascular inflammation and other mechanisms. Several transcription factors are activated upon diabetes-driven endothelial dysfunction and drive the progression of atherosclerosis. In particular, the hypoxia-inducible factor (HIF) transcription factor family is a master regulator of endothelial biology and is raising interest in the field of atherosclerosis. In this review, we will present an overview of studies contributing to the understanding of diabetes-driven atherosclerosis, integrating the role of HIF in this disease with the knowledge of its functions in metabolic syndrome and diabetic scenario.

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