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Drug Discovery in Liver Disease Using Kinome Profiling

The liver is one of the most important organs, playing critical roles in maintaining biochemical homeostasis. Accordingly, disease of the liver is often debilitating and responsible for untold human misery. As biochemical nexus, with kinases being master regulators of cellular biochemistry, targetin...

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Autores principales: Yu, Bingting, Mamedov, Ruslan, Fuhler, Gwenny M., Peppelenbosch, Maikel P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961955/
https://www.ncbi.nlm.nih.gov/pubmed/33807722
http://dx.doi.org/10.3390/ijms22052623
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author Yu, Bingting
Mamedov, Ruslan
Fuhler, Gwenny M.
Peppelenbosch, Maikel P.
author_facet Yu, Bingting
Mamedov, Ruslan
Fuhler, Gwenny M.
Peppelenbosch, Maikel P.
author_sort Yu, Bingting
collection PubMed
description The liver is one of the most important organs, playing critical roles in maintaining biochemical homeostasis. Accordingly, disease of the liver is often debilitating and responsible for untold human misery. As biochemical nexus, with kinases being master regulators of cellular biochemistry, targeting kinase enzymes is an obvious avenue for treating liver disease. Development of such therapy, however, is hampered by the technical difficulty of obtaining comprehensive insight into hepatic kinase activity, a problem further compounded by the often unique aspects of hepatic kinase activities, which makes extrapolations from other systems difficult. This consideration prompted us to review the current state of the art with respect to kinome profiling approaches towards the hepatic kinome. We observe that currently four different approaches are available, all showing significant promise. Hence we postulate that insight into the hepatic kinome will quickly increase, leading to rational kinase-targeted therapy for different liver diseases.
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spelling pubmed-79619552021-03-17 Drug Discovery in Liver Disease Using Kinome Profiling Yu, Bingting Mamedov, Ruslan Fuhler, Gwenny M. Peppelenbosch, Maikel P. Int J Mol Sci Review The liver is one of the most important organs, playing critical roles in maintaining biochemical homeostasis. Accordingly, disease of the liver is often debilitating and responsible for untold human misery. As biochemical nexus, with kinases being master regulators of cellular biochemistry, targeting kinase enzymes is an obvious avenue for treating liver disease. Development of such therapy, however, is hampered by the technical difficulty of obtaining comprehensive insight into hepatic kinase activity, a problem further compounded by the often unique aspects of hepatic kinase activities, which makes extrapolations from other systems difficult. This consideration prompted us to review the current state of the art with respect to kinome profiling approaches towards the hepatic kinome. We observe that currently four different approaches are available, all showing significant promise. Hence we postulate that insight into the hepatic kinome will quickly increase, leading to rational kinase-targeted therapy for different liver diseases. MDPI 2021-03-05 /pmc/articles/PMC7961955/ /pubmed/33807722 http://dx.doi.org/10.3390/ijms22052623 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yu, Bingting
Mamedov, Ruslan
Fuhler, Gwenny M.
Peppelenbosch, Maikel P.
Drug Discovery in Liver Disease Using Kinome Profiling
title Drug Discovery in Liver Disease Using Kinome Profiling
title_full Drug Discovery in Liver Disease Using Kinome Profiling
title_fullStr Drug Discovery in Liver Disease Using Kinome Profiling
title_full_unstemmed Drug Discovery in Liver Disease Using Kinome Profiling
title_short Drug Discovery in Liver Disease Using Kinome Profiling
title_sort drug discovery in liver disease using kinome profiling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961955/
https://www.ncbi.nlm.nih.gov/pubmed/33807722
http://dx.doi.org/10.3390/ijms22052623
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