Cargando…

Current Status in the Therapy of Liver Diseases

Hepatic diseases, like viral hepatitis, autoimmune hepatitis, hereditary hemochromatosis, non-alcoholic fatty liver disease (NAFLD) and Wilson’s disease, play an important role in the development of liver cirrhosis and, hence, hepatocellular carcinoma. In this review, the current treatment options a...

Descripción completa

Detalles Bibliográficos
Autores principales: Uhl, Philipp, Fricker, Gert, Haberkorn, Uwe, Mier, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057686/
https://www.ncbi.nlm.nih.gov/pubmed/24786290
http://dx.doi.org/10.3390/ijms15057500
_version_ 1782321010289147904
author Uhl, Philipp
Fricker, Gert
Haberkorn, Uwe
Mier, Walter
author_facet Uhl, Philipp
Fricker, Gert
Haberkorn, Uwe
Mier, Walter
author_sort Uhl, Philipp
collection PubMed
description Hepatic diseases, like viral hepatitis, autoimmune hepatitis, hereditary hemochromatosis, non-alcoholic fatty liver disease (NAFLD) and Wilson’s disease, play an important role in the development of liver cirrhosis and, hence, hepatocellular carcinoma. In this review, the current treatment options and the molecular mechanisms of action of the drugs are summarized. Unfortunately, the treatment options for most of these hepatic diseases are limited. Since hepatitis B (HBV) and C (HCV) infections are the most common causes of liver cirrhosis and hepatocellular carcinoma, they are the focus of the development of new drugs. The current treatment of choice for HBV/HCV infection is an interferon-based combination therapy with oral antiviral drugs, like nucleos(t)ide analogues, which is associated with improving the therapeutic success and also preventing the development of resistances. Currently, two new protease inhibitors for HCV treatment are expected (deleobuvir, faldaprevir) and together with the promising drug, daclatasvir (NS5A-inhibitor, currently in clinical trials), adequate therapy is to be expected in due course (circumventing the requirement of interferon with its side-effects), while in contrast, efficient HBV therapeutics are still lacking. In this respect, entry inhibitors, like Myrcludex B, the lead substance of the first entry inhibitor for HBV/HDV (hepatitis D) infection, provide immense potential. The pharmacokinetics and the mechanism of action of Myrcludex B are described in detail.
format Online
Article
Text
id pubmed-4057686
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Molecular Diversity Preservation International (MDPI)
record_format MEDLINE/PubMed
spelling pubmed-40576862014-06-16 Current Status in the Therapy of Liver Diseases Uhl, Philipp Fricker, Gert Haberkorn, Uwe Mier, Walter Int J Mol Sci Review Hepatic diseases, like viral hepatitis, autoimmune hepatitis, hereditary hemochromatosis, non-alcoholic fatty liver disease (NAFLD) and Wilson’s disease, play an important role in the development of liver cirrhosis and, hence, hepatocellular carcinoma. In this review, the current treatment options and the molecular mechanisms of action of the drugs are summarized. Unfortunately, the treatment options for most of these hepatic diseases are limited. Since hepatitis B (HBV) and C (HCV) infections are the most common causes of liver cirrhosis and hepatocellular carcinoma, they are the focus of the development of new drugs. The current treatment of choice for HBV/HCV infection is an interferon-based combination therapy with oral antiviral drugs, like nucleos(t)ide analogues, which is associated with improving the therapeutic success and also preventing the development of resistances. Currently, two new protease inhibitors for HCV treatment are expected (deleobuvir, faldaprevir) and together with the promising drug, daclatasvir (NS5A-inhibitor, currently in clinical trials), adequate therapy is to be expected in due course (circumventing the requirement of interferon with its side-effects), while in contrast, efficient HBV therapeutics are still lacking. In this respect, entry inhibitors, like Myrcludex B, the lead substance of the first entry inhibitor for HBV/HDV (hepatitis D) infection, provide immense potential. The pharmacokinetics and the mechanism of action of Myrcludex B are described in detail. Molecular Diversity Preservation International (MDPI) 2014-04-30 /pmc/articles/PMC4057686/ /pubmed/24786290 http://dx.doi.org/10.3390/ijms15057500 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Uhl, Philipp
Fricker, Gert
Haberkorn, Uwe
Mier, Walter
Current Status in the Therapy of Liver Diseases
title Current Status in the Therapy of Liver Diseases
title_full Current Status in the Therapy of Liver Diseases
title_fullStr Current Status in the Therapy of Liver Diseases
title_full_unstemmed Current Status in the Therapy of Liver Diseases
title_short Current Status in the Therapy of Liver Diseases
title_sort current status in the therapy of liver diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057686/
https://www.ncbi.nlm.nih.gov/pubmed/24786290
http://dx.doi.org/10.3390/ijms15057500
work_keys_str_mv AT uhlphilipp currentstatusinthetherapyofliverdiseases
AT frickergert currentstatusinthetherapyofliverdiseases
AT haberkornuwe currentstatusinthetherapyofliverdiseases
AT mierwalter currentstatusinthetherapyofliverdiseases