Hypoxia-inducible factors as molecular targets for liver diseases

被引:118
|
作者
Ju, Cynthia [1 ]
Colgan, Sean P. [2 ]
Eltzschig, Holger K. [3 ]
机构
[1] Univ Colorado, Skaggs Sch Pharm, Dept Pharmaceut Sci, Aurora, CO USA
[2] Univ Colorado, Sch Med, Dept Med & Mucosal Inflammat Program, Aurora, CO USA
[3] Univ Colorado, Sch Med, Dept Anesthesiol & Organ Protect Program, Aurora, CO USA
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2016年 / 94卷 / 06期
关键词
HIF1; alpha; HIF2; Ischemia-reperfusion liver injury; Fatty liver; Viral hepatitis; Alcoholic liver disease; Hepatocellular carcinoma; HEPATITIS-C VIRUS; ISCHEMIA-REPERFUSION INJURY; ACTIVATED PROTEIN-KINASE; ADENOSINE A(2A) RECEPTOR; HEPATOCELLULAR-CARCINOMA; FATTY LIVER; X PROTEIN; UP-REGULATION; NONALCOHOLIC STEATOHEPATITIS; LIPID-ACCUMULATION;
D O I
10.1007/s00109-016-1408-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:613 / 627
页数:15
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