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Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis

Schistosomiasis is a major neglected parasitic disease that affects more than 240 million people worldwide and for which the control strategy consists of mass treatment with the only available drug, praziquantel. Schistosomes display morphologically distinct stages during their life cycle and the tr...

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Autores principales: Ghazy, Ehab, Abdelsalam, Mohamed, Robaa, Dina, Pierce, Raymond J., Sippl, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779837/
https://www.ncbi.nlm.nih.gov/pubmed/35056137
http://dx.doi.org/10.3390/ph15010080
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author Ghazy, Ehab
Abdelsalam, Mohamed
Robaa, Dina
Pierce, Raymond J.
Sippl, Wolfgang
author_facet Ghazy, Ehab
Abdelsalam, Mohamed
Robaa, Dina
Pierce, Raymond J.
Sippl, Wolfgang
author_sort Ghazy, Ehab
collection PubMed
description Schistosomiasis is a major neglected parasitic disease that affects more than 240 million people worldwide and for which the control strategy consists of mass treatment with the only available drug, praziquantel. Schistosomes display morphologically distinct stages during their life cycle and the transformations between stages are controlled by epigenetic mechanisms. The targeting of epigenetic actors might therefore represent the parasites’ Achilles’ heel. Specifically, histone deacetylases have been recently characterized as drug targets for the treatment of schistosomiasis. This review focuses on the recent development of inhibitors for schistosome histone deacetylases. In particular, advances in the development of inhibitors of Schistosoma mansoni histone deacetylase 8 have indicated that targeting this enzyme is a promising approach for the treatment of this infection.
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spelling pubmed-87798372022-01-22 Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis Ghazy, Ehab Abdelsalam, Mohamed Robaa, Dina Pierce, Raymond J. Sippl, Wolfgang Pharmaceuticals (Basel) Review Schistosomiasis is a major neglected parasitic disease that affects more than 240 million people worldwide and for which the control strategy consists of mass treatment with the only available drug, praziquantel. Schistosomes display morphologically distinct stages during their life cycle and the transformations between stages are controlled by epigenetic mechanisms. The targeting of epigenetic actors might therefore represent the parasites’ Achilles’ heel. Specifically, histone deacetylases have been recently characterized as drug targets for the treatment of schistosomiasis. This review focuses on the recent development of inhibitors for schistosome histone deacetylases. In particular, advances in the development of inhibitors of Schistosoma mansoni histone deacetylase 8 have indicated that targeting this enzyme is a promising approach for the treatment of this infection. MDPI 2022-01-10 /pmc/articles/PMC8779837/ /pubmed/35056137 http://dx.doi.org/10.3390/ph15010080 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ghazy, Ehab
Abdelsalam, Mohamed
Robaa, Dina
Pierce, Raymond J.
Sippl, Wolfgang
Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis
title Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis
title_full Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis
title_fullStr Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis
title_full_unstemmed Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis
title_short Histone Deacetylase (HDAC) Inhibitors for the Treatment of Schistosomiasis
title_sort histone deacetylase (hdac) inhibitors for the treatment of schistosomiasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779837/
https://www.ncbi.nlm.nih.gov/pubmed/35056137
http://dx.doi.org/10.3390/ph15010080
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