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Drug repurposing and human parasitic protozoan diseases

Parasitic diseases have an enormous health, social and economic impact and are a particular problem in tropical regions of the world. Diseases caused by protozoa and helminths, such as malaria and schistosomiasis, are the cause of most parasite related morbidity and mortality, with an estimated 1.1 ...

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Detalles Bibliográficos
Autores principales: Andrews, Katherine T., Fisher, Gillian, Skinner-Adams, Tina S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095053/
https://www.ncbi.nlm.nih.gov/pubmed/25057459
http://dx.doi.org/10.1016/j.ijpddr.2014.02.002
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author Andrews, Katherine T.
Fisher, Gillian
Skinner-Adams, Tina S.
author_facet Andrews, Katherine T.
Fisher, Gillian
Skinner-Adams, Tina S.
author_sort Andrews, Katherine T.
collection PubMed
description Parasitic diseases have an enormous health, social and economic impact and are a particular problem in tropical regions of the world. Diseases caused by protozoa and helminths, such as malaria and schistosomiasis, are the cause of most parasite related morbidity and mortality, with an estimated 1.1 million combined deaths annually. The global burden of these diseases is exacerbated by the lack of licensed vaccines, making safe and effective drugs vital to their prevention and treatment. Unfortunately, where drugs are available, their usefulness is being increasingly threatened by parasite drug resistance. The need for new drugs drives antiparasitic drug discovery research globally and requires a range of innovative strategies to ensure a sustainable pipeline of lead compounds. In this review we discuss one of these approaches, drug repurposing or repositioning, with a focus on major human parasitic protozoan diseases such as malaria, trypanosomiasis, toxoplasmosis, cryptosporidiosis and leishmaniasis.
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spelling pubmed-40950532014-07-23 Drug repurposing and human parasitic protozoan diseases Andrews, Katherine T. Fisher, Gillian Skinner-Adams, Tina S. Int J Parasitol Drugs Drug Resist Invited Review Parasitic diseases have an enormous health, social and economic impact and are a particular problem in tropical regions of the world. Diseases caused by protozoa and helminths, such as malaria and schistosomiasis, are the cause of most parasite related morbidity and mortality, with an estimated 1.1 million combined deaths annually. The global burden of these diseases is exacerbated by the lack of licensed vaccines, making safe and effective drugs vital to their prevention and treatment. Unfortunately, where drugs are available, their usefulness is being increasingly threatened by parasite drug resistance. The need for new drugs drives antiparasitic drug discovery research globally and requires a range of innovative strategies to ensure a sustainable pipeline of lead compounds. In this review we discuss one of these approaches, drug repurposing or repositioning, with a focus on major human parasitic protozoan diseases such as malaria, trypanosomiasis, toxoplasmosis, cryptosporidiosis and leishmaniasis. Elsevier 2014-03-24 /pmc/articles/PMC4095053/ /pubmed/25057459 http://dx.doi.org/10.1016/j.ijpddr.2014.02.002 Text en © 2014 Published by Elsevier Ltd on behalf of Australian Society for Parasitology. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Invited Review
Andrews, Katherine T.
Fisher, Gillian
Skinner-Adams, Tina S.
Drug repurposing and human parasitic protozoan diseases
title Drug repurposing and human parasitic protozoan diseases
title_full Drug repurposing and human parasitic protozoan diseases
title_fullStr Drug repurposing and human parasitic protozoan diseases
title_full_unstemmed Drug repurposing and human parasitic protozoan diseases
title_short Drug repurposing and human parasitic protozoan diseases
title_sort drug repurposing and human parasitic protozoan diseases
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095053/
https://www.ncbi.nlm.nih.gov/pubmed/25057459
http://dx.doi.org/10.1016/j.ijpddr.2014.02.002
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