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Hypoxia-inducible factors as molecular targets for liver diseases

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TLDR
The evidence for HIF stabilization in liver disease is summarized, the mechanistic involvement of HIFs in disease development is discussed, and the potential of pharmacological HIF modifiers in the treatment of liver disease are explored.
Abstract
Liver disease is a growing global health problem, as deaths from end-stage liver cirrhosis and cancer are rising across the world. At present, pharmacologic approaches to effectively treat or prevent liver disease are extremely limited. Hypoxia-inducible factor (HIF) is a transcription factor that regulates diverse signaling pathways enabling adaptive cellular responses to perturbations of the tissue microenvironment. HIF activation through hypoxia-dependent and hypoxia-independent signals have been reported in liver disease of diverse etiologies, from ischemia-reperfusion-induced acute liver injury to chronic liver diseases caused by viral infection, excessive alcohol consumption, or metabolic disorders. This review summarizes the evidence for HIF stabilization in liver disease, discusses the mechanistic involvement of HIFs in disease development, and explores the potential of pharmacological HIF modifiers in the treatment of liver disease.

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Journal ArticleDOI

Hypoxia signaling in human diseases and therapeutic targets.

TL;DR: The role of HIF stabilization during hypoxia has been extended from the induction of a single gene erythropoietin to the upregulation of a couple of hundred downstream targets, which demonstrates the complexity and importance of the HIF signaling pathway.
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Sorafenib resistance in hepatocarcinoma: role of hypoxia-inducible factors

TL;DR: There is a marked correlation between the hypoxic microenvironment and sorafenib resistance, suggesting that targeting HIFs is a promising way to increase the efficiency of treatment.
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Ischaemia reperfusion injury in liver transplantation: Cellular and molecular mechanisms.

TL;DR: Understanding the relationship of the clinical risk factors for liver IRI to the cellular and molecular mechanisms that govern it is critical to higher levels of success after liver transplantation – a process that will lead to improved outcomes for patients suffering from end‐stage liver disease.
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An ALOX12–12-HETE–GPR31 signaling axis is a key mediator of hepatic ischemia–reperfusion injury

TL;DR: This study has revealed previously uncharacterized metabolic reprogramming involving an ALOX12–12-HETE–GPR31 axis that functionally determines hepatic IR procession and provided proof of concept that blocking 12- HETE production is a promising strategy for preventing and treating IR-induced liver damage.
References
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