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Hypoxia-inducible factors and the regulation of lipid metabolism

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Autor
Mylonis I., Simos G., Paraskeva E.
Fecha
2019
Language
en
DOI
10.3390/cells8030214
Materia
adipophilin
ATM protein
carnitine palmitoyltransferase
casein kinase Idelta
fatty acid
fatty acid binding protein 3
fatty acid binding protein 4
fatty acid binding protein 7
glucose transporter 1
glucose transporter 3
glutaminase
hypoxia inducible factor
hypoxia inducible factor proline dioxygenase
lysophosphatidic acid
lysophosphatidic acid receptor
oxidized low density lipoprotein receptor 1
oxoglutarate dehydrogenase
peroxisome proliferator activated receptor alpha
peroxisome proliferator activated receptor gamma coactivator 1alpha
peroxisome proliferator activated receptor gamma coactivator 1beta
STAT3 protein
triacylglycerol
triacylglycerol lipase
very low density lipoprotein receptor
anaerobic glycolysis
biosynthesis
cancer growth
carbohydrate metabolism
cardiovascular disease
catabolism
cell proliferation assay
cell survival
gene overexpression
hepatomegaly
human
lipid metabolism
lipid storage
lipotoxicity
liver cell carcinoma
metabolic disorder
metabolic regulation
metabolic syndrome X
nonalcoholic fatty liver
nonhuman
obesity
pathological anatomy
Pi3K/Akt signaling
protein modification
protein phosphorylation
protein synthesis
Review
transactivation
MDPI
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Resumen
Oxygen deprivation or hypoxia characterizes a number of serious pathological conditions and elicits a number of adaptive changes that are mainly mediated at the transcriptional level by the family of hypoxia-inducible factors (HIFs). The HIF target gene repertoire includes genes responsible for the regulation of metabolism, oxygen delivery and cell survival. Although the involvement of HIFs in the regulation of carbohydrate metabolism and the switch to anaerobic glycolysis under hypoxia is well established, their role in the control of lipid anabolism and catabolism remains still relatively obscure. Recent evidence indicates that many aspects of lipid metabolism are modified during hypoxia or in tumor cells in a HIF-dependent manner, contributing significantly to the pathogenesis and/or progression of cancer and metabolic disorders. However, direct transcriptional regulation by HIFs has been only demonstrated in relatively few cases, leaving open the exact and isoform-specific mechanisms that underlie HIF-dependency. This review summarizes the evidence for both direct and indirect roles of HIFs in the regulation of genes involved in lipid metabolism as well as the involvement of HIFs in various diseases as demonstrated by studies with transgenic animal models. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/76851
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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