Modulation of autophagy for the treatment of liver diseases

被引:68
作者
Gracia-Sancho, Jordi [1 ]
Guixe-Muntet, Sergi [1 ]
Hide, Diana [1 ]
Bosch, Jaime [1 ]
机构
[1] Hosp Clin Barcelona, CIBEREHD, Inst Invest Biomed August Pi & Sunyer IDIBAPS, Barcelona Hepat Hemodynam Lab, Barcelona, Spain
关键词
chloroquine; cirrhosis; hepatic; ischemia; non-alcoholic fatty liver disease; HEPATITIS-C VIRUS; ENDOPLASMIC-RETICULUM STRESS; ISCHEMIA-REPERFUSION INJURY; HEPATOCELLULAR-CARCINOMA; FATTY LIVER; INDUCED APOPTOSIS; B-VIRUS; ISCHEMIA/REPERFUSION INJURY; MAMMALIAN TARGET; DOWN-REGULATION;
D O I
10.1517/13543784.2014.912274
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Autophagy is a cellular process essential for survival and homeostasis that confers cellular protection toward a wide range of deleterious stimuli. It has a highly complex regulation with several autophagic proteins also belonging to other main signaling pathways as cell proliferation or apoptosis. In addition, autophagy has an important role in cell metabolism. Interest in the study of this process is rapidly rising and, in the past few years, autophagy has been implicated in a variety of hepatic diseases. Areas covered: The review covers the research and investigational use of pharmacological strategies that modify autophagy in the treatment of liver diseases. Autophagy modulation in steatosis, steatohepatitis, viral hepatitis, fibrogenesis, cirrhosis, hepatocellular carcinoma and ischemia/reperfusion injury will be described, critically analyzed and discussed. Papers included in the present manuscript were selected from the PubMed search: liver + (macro) autophagy + each of the pathologies described above. Expert opinion: The complexity of autophagy creates significant controversy on the potential of its pharmacological modulation. A major requirement for drugs regulating autophagy in the treatment of liver diseases is that these should be liver-specific; moreover, they should primarily target one specific hepatic cell type.
引用
收藏
页码:965 / 977
页数:13
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