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Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future

Malaria is still one of the major killer parasitic diseases in tropical settings, posing a public health threat. The development of antimalarial drug resistance is reversing the gains made in attempts to control the disease. The parasite leads a complex life cycle that has adapted to outwit almost a...

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Autores principales: Stofberg, Melissa Louise, Caillet, Celine, de Villiers, Marianne, Zininga, Tawanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616389/
https://www.ncbi.nlm.nih.gov/pubmed/34831072
http://dx.doi.org/10.3390/cells10112849
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author Stofberg, Melissa Louise
Caillet, Celine
de Villiers, Marianne
Zininga, Tawanda
author_facet Stofberg, Melissa Louise
Caillet, Celine
de Villiers, Marianne
Zininga, Tawanda
author_sort Stofberg, Melissa Louise
collection PubMed
description Malaria is still one of the major killer parasitic diseases in tropical settings, posing a public health threat. The development of antimalarial drug resistance is reversing the gains made in attempts to control the disease. The parasite leads a complex life cycle that has adapted to outwit almost all known antimalarial drugs to date, including the first line of treatment, artesunate. There is a high unmet need to develop new strategies and identify novel therapeutics to reverse antimalarial drug resistance development. Among the strategies, here we focus and discuss the merits of the development of antimalarials targeting the Heat shock protein 90 (Hsp90) due to the central role it plays in protein quality control.
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spelling pubmed-86163892021-11-26 Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future Stofberg, Melissa Louise Caillet, Celine de Villiers, Marianne Zininga, Tawanda Cells Review Malaria is still one of the major killer parasitic diseases in tropical settings, posing a public health threat. The development of antimalarial drug resistance is reversing the gains made in attempts to control the disease. The parasite leads a complex life cycle that has adapted to outwit almost all known antimalarial drugs to date, including the first line of treatment, artesunate. There is a high unmet need to develop new strategies and identify novel therapeutics to reverse antimalarial drug resistance development. Among the strategies, here we focus and discuss the merits of the development of antimalarials targeting the Heat shock protein 90 (Hsp90) due to the central role it plays in protein quality control. MDPI 2021-10-22 /pmc/articles/PMC8616389/ /pubmed/34831072 http://dx.doi.org/10.3390/cells10112849 Text en © 2021 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
Stofberg, Melissa Louise
Caillet, Celine
de Villiers, Marianne
Zininga, Tawanda
Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future
title Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future
title_full Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future
title_fullStr Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future
title_full_unstemmed Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future
title_short Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future
title_sort inhibitors of the plasmodium falciparum hsp90 towards selective antimalarial drug design: the past, present and future
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616389/
https://www.ncbi.nlm.nih.gov/pubmed/34831072
http://dx.doi.org/10.3390/cells10112849
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