Literature DB >> 24749698

Modulation of autophagy for the treatment of liver diseases.

Jordi Gracia-Sancho1, Sergi Guixé-Muntet, Diana Hide, Jaime Bosch.   

Abstract

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.

Entities:  

Keywords:  chloroquine; cirrhosis; hepatic; ischemia; non-alcoholic fatty liver disease

Mesh:

Year:  2014        PMID: 24749698     DOI: 10.1517/13543784.2014.912274

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  13 in total

Review 1.  Relevance of autophagy to fatty liver diseases and potential therapeutic applications.

Authors:  Shengmin Yan; Nazmul Huda; Bilon Khambu; Xiao-Ming Yin
Journal:  Amino Acids       Date:  2017-05-06       Impact factor: 3.520

2.  Transient receptor potential vanilloid 4 inhibits rat HSC-T6 apoptosis through induction of autophagy.

Authors:  Lei Zhan; Yang Yang; Tao-Tao Ma; Cheng Huang; Xiao-Ming Meng; Lei Zhang; Jun Li
Journal:  Mol Cell Biochem       Date:  2015-01-20       Impact factor: 3.396

3.  Reactive Oxygen Species-Mediated c-Jun NH2-Terminal Kinase Activation Contributes to Hepatitis B Virus X Protein-Induced Autophagy via Regulation of the Beclin-1/Bcl-2 Interaction.

Authors:  Linmao Zhong; Wangqin Shu; Wangbin Dai; Bo Gao; Sidong Xiong
Journal:  J Virol       Date:  2017-07-12       Impact factor: 5.103

4.  ASPP2 inhibits hepatitis B virus replication by preventing nucleus translocation of HSF1 and attenuating the transactivation of ATG7.

Authors:  Shanshan Wang; Yu Sun; Yang Wang; Anna Wang; Buxin Kou; Yang Che; Dexi Chen; Yulin Zhang; Ying Shi
Journal:  J Cell Mol Med       Date:  2021-06-04       Impact factor: 5.310

5.  Epigallocatechin-3-gallate opposes HBV-induced incomplete autophagy by enhancing lysosomal acidification, which is unfavorable for HBV replication.

Authors:  L Zhong; J Hu; W Shu; B Gao; S Xiong
Journal:  Cell Death Dis       Date:  2015-05-21       Impact factor: 8.469

Review 6.  Traditional Chinese herbal extracts inducing autophagy as a novel approach in therapy of nonalcoholic fatty liver disease.

Authors:  Cong Liu; Jia-Zhi Liao; Pei-Yuan Li
Journal:  World J Gastroenterol       Date:  2017-03-21       Impact factor: 5.742

7.  Celecoxib alleviates nonalcoholic fatty liver disease by restoring autophagic flux.

Authors:  Cong Liu; Lian Liu; Hai-Dan Zhu; Jia-Qi Sheng; Xiao-Li Wu; Xing-Xing He; De-An Tian; Jia-Zhi Liao; Pei-Yuan Li
Journal:  Sci Rep       Date:  2018-03-07       Impact factor: 4.379

Review 8.  Autophagy: a new target for nonalcoholic fatty liver disease therapy.

Authors:  Yuqing Mao; Fujun Yu; Jianbo Wang; Chuanyong Guo; Xiaoming Fan
Journal:  Hepat Med       Date:  2016-03-24

9.  Autophagy and Akt in the protective effect of erythropoietin helix B surface peptide against hepatic ischaemia/reperfusion injury in mice.

Authors:  Rumeng Tan; Hongzhe Tian; Bo Yang; Bo Zhang; Chen Dai; Zhenyi Han; Meixi Wang; Yakun Li; Lai Wei; Dong Chen; Guangyao Wang; Huifang Yang; Fan He; Zhishui Chen
Journal:  Sci Rep       Date:  2018-10-02       Impact factor: 4.379

10.  PPARγ Plays an Important Role in Acute Hepatic Ischemia-Reperfusion Injury via AMPK/mTOR Pathway.

Authors:  Liwei Wu; Qiang Yu; Ping Cheng; Chuanyong Guo
Journal:  PPAR Res       Date:  2021-07-03       Impact factor: 4.964

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