Literature DB >> 31692390

Progress in promising anti-fibrotic therapies.

Rosanna Santoro1, Alessandra Mangia1.   

Abstract

Introduction: Liver cirrhosis is the most deleterious consequence of chronic liver diseases of different etiologies. Progression of liver diseases to cirrhosis, irrespective of etiology, involves chronic parenchymal injury, persistent activation of inflammatory response, sustained activation of fibrogenesis and wound-healing response. Despite intensive research on antifibrotic drugs, novel therapeutics specifically for liver have not been yet licensed. This review will examine compounds currently under development and key challenges in specific settings as for example that of NAFLD associated fibrosis.Areas covered: Results of the main phase II and III trial, including those with negative results, are presented and discussed. The endpoints selected and their limitations highlighted in order to suggest potential options to move forward.Expert opinion: Strategies based on single-molecule targets, associated so far with some disappointing results, may be unlikely to succeed in the context of such complex pathogenesis. Blocking at the same time different pathways that drive fibrosis progression may be required to provide significant benefit.

Entities:  

Keywords:  FXR; Fibrosis; NAFLD; apoptosis; chemokine; diabetes; insulin sensitizing drugs; lipotoxicity; nuclear receptors; steatohepatitis (NASH)

Mesh:

Year:  2019        PMID: 31692390     DOI: 10.1080/17474124.2019.1688659

Source DB:  PubMed          Journal:  Expert Rev Gastroenterol Hepatol        ISSN: 1747-4124            Impact factor:   3.869


  4 in total

1.  Strategies Targeting the Innate Immune Response for the Treatment of Hepatitis C Virus-Associated Liver Fibrosis.

Authors:  Daniel Sepulveda-Crespo; Salvador Resino; Isidoro Martinez
Journal:  Drugs       Date:  2021-01-05       Impact factor: 9.546

Review 2.  An Update on Efficacy and Safety of Emerging Hepatic Antifibrotic Agents.

Authors:  Vinka Rupcic Rubin; Kristina Bojanic; Martina Smolic; Jurica Rubin; Ashraf Tabll; Robert Smolic
Journal:  J Clin Transl Hepatol       Date:  2021-01-04

3.  Complexation with Random Methyl-β-Cyclodextrin and (2-Hidroxypropyl)-β-Cyclodextrin Enhances In Vivo Anti-Fibrotic and Anti-Inflammatory Effects of Chrysin via the Inhibition of NF-κB and TGF-β1/Smad Signaling Pathways and Modulation of Hepatic Pro/Anti-Fibrotic miRNA.

Authors:  Alina Ciceu; Cornel Balta; Hidegard Herman; Sami Gharbia; Simona-Rebeca Ignat; Sorina Dinescu; Judit Váradi; Ferenc Fenyvesi; Szilvia Gyöngyösi; Anca Hermenean; Marieta Costache
Journal:  Int J Mol Sci       Date:  2021-02-13       Impact factor: 5.923

Review 4.  Gasotransmitters: Potential Therapeutic Molecules of Fibrotic Diseases.

Authors:  Yingqing Chen; Shuo Yuan; Yuying Cao; Guangyao Kong; Feng Jiang; You Li; Qi Wang; Minli Tang; Qinggao Zhang; Qianqian Wang; Liping Liu
Journal:  Oxid Med Cell Longev       Date:  2021-09-20       Impact factor: 6.543

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.