Literature DB >> 32543284

Current and emerging pharmacotherapeutic interventions for the treatment of liver fibrosis.

Joeri Lambrecht1, Leo A van Grunsven1, Frank Tacke2.   

Abstract

INTRODUCTION: Chronic liver disease is due to various causes of persistent liver damage and will eventually lead to the development of liver fibrosis. If no treatment is initiated, this condition may progress to cirrhosis and hepatocellular carcinoma. Current treatments comprise the elimination of the cause of injury, such as by lifestyle changes, alcohol abstinence, and antiviral agents. However, such etiology-driven therapy is often insufficient in patients with late-stage fibrosis/cirrhosis, therefore maintaining the need for efficient antifibrotic pharmacotherapeutic interventions. AREAS COVERED: The authors discuss the recent advances in the development of antifibrotic drugs, which target various pathways of the fibrogenesis process, including cell death, inflammation, gut-liver axis, and myofibroblast activation. Due to the significant burden of nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH), various agents which specifically target metabolic pathways and their related receptors/ligands have been developed. For some of them, e.g., obeticholic acid, advanced stage clinical trials indicate antifibrotic efficacy in NAFLD and NASH. EXPERT OPINION: Significant advances have been made in the development of novel antifibrotic pharmacotherapeutics. The authors expect that the development of combinatorial therapies, which combine compounds that target various pathways of fibrosis progression, will have a major impact as future etiology-independent therapies.

Entities:  

Keywords:  Apoptosis; FXR; NAFLD; NASH; PPAR; gut-liver axis; hepatic stellate cell; molecular targets; myofibroblast; nuclear receptor; regression

Mesh:

Year:  2020        PMID: 32543284     DOI: 10.1080/14656566.2020.1774553

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  13 in total

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Review 5.  Nuclear Receptors Linking Metabolism, Inflammation, and Fibrosis in Nonalcoholic Fatty Liver Disease.

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6.  Coordinated signaling of activating transcription factor 6α and inositol-requiring enzyme 1α regulates hepatic stellate cell-mediated fibrogenesis in mice.

Authors:  Fei Xue; Jianwen Lu; Samuel C Buchl; Liankang Sun; Vijay H Shah; Harmeet Malhi; Jessica L Maiers
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7.  Smad3 gene C-terminal phosphorylation site mutation exacerbates CCl4-induced hepatic fibrogenesis by promoting pSmad2L/C-mediated signaling transduction.

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Authors:  Joeri Lambrecht; Frank Tacke
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2020-07-27

Review 10.  Liver Injury and the Macrophage Issue: Molecular and Mechanistic Facts and Their Clinical Relevance.

Authors:  Siyer Roohani; Frank Tacke
Journal:  Int J Mol Sci       Date:  2021-07-06       Impact factor: 5.923

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