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Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis?
Leishmaniasis is a neglected disease, which needs improvements in drug development, mainly due to the toxicity, parasite resistance and low compliance of patients to treatment. Therefore, the development of new chemotherapeutic compounds is an urgent need. This opinion article will briefly highlight...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300003/ https://www.ncbi.nlm.nih.gov/pubmed/27869056 http://dx.doi.org/10.1017/S003118201600189X |
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author | ENNES-VIDAL, VITOR MENNA-BARRETO, RUBEM FIGUEIREDO SADOCK BRANQUINHA, MARTA HELENA DOS SANTOS, ANDRÉ LUIS SOUZA D'AVILA-LEVY, CLAUDIA MASINI |
author_facet | ENNES-VIDAL, VITOR MENNA-BARRETO, RUBEM FIGUEIREDO SADOCK BRANQUINHA, MARTA HELENA DOS SANTOS, ANDRÉ LUIS SOUZA D'AVILA-LEVY, CLAUDIA MASINI |
author_sort | ENNES-VIDAL, VITOR |
collection | PubMed |
description | Leishmaniasis is a neglected disease, which needs improvements in drug development, mainly due to the toxicity, parasite resistance and low compliance of patients to treatment. Therefore, the development of new chemotherapeutic compounds is an urgent need. This opinion article will briefly highlight the feasible use of calpain inhibitors as leading compounds to search for new therapeutic options to treat leishmaniasis. The milestone of this approach is to take advantage on the myriad of inhibitors developed against calpains, some of which are in advanced clinical trials. The deregulated activity of these enzymes is associated with several pathologies, such as strokes, diabetes and Parkinson's disease, to name a few. In Leishmania, calpain upregulation has been associated to drug resistance and virulence. Whereas the difficulties in developing new drugs for neglected diseases are more economical than biotechnological, repurposing approach with compounds already approved for clinical use by the regulatory agencies can be an interesting shortcut to a successful chemotherapeutic treatment for leishmaniasis. |
format | Online Article Text |
id | pubmed-5300003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53000032017-02-16 Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? ENNES-VIDAL, VITOR MENNA-BARRETO, RUBEM FIGUEIREDO SADOCK BRANQUINHA, MARTA HELENA DOS SANTOS, ANDRÉ LUIS SOUZA D'AVILA-LEVY, CLAUDIA MASINI Parasitology Review Article Leishmaniasis is a neglected disease, which needs improvements in drug development, mainly due to the toxicity, parasite resistance and low compliance of patients to treatment. Therefore, the development of new chemotherapeutic compounds is an urgent need. This opinion article will briefly highlight the feasible use of calpain inhibitors as leading compounds to search for new therapeutic options to treat leishmaniasis. The milestone of this approach is to take advantage on the myriad of inhibitors developed against calpains, some of which are in advanced clinical trials. The deregulated activity of these enzymes is associated with several pathologies, such as strokes, diabetes and Parkinson's disease, to name a few. In Leishmania, calpain upregulation has been associated to drug resistance and virulence. Whereas the difficulties in developing new drugs for neglected diseases are more economical than biotechnological, repurposing approach with compounds already approved for clinical use by the regulatory agencies can be an interesting shortcut to a successful chemotherapeutic treatment for leishmaniasis. Cambridge University Press 2017-02 2016-11-21 /pmc/articles/PMC5300003/ /pubmed/27869056 http://dx.doi.org/10.1017/S003118201600189X Text en © Cambridge University Press 2016 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article ENNES-VIDAL, VITOR MENNA-BARRETO, RUBEM FIGUEIREDO SADOCK BRANQUINHA, MARTA HELENA DOS SANTOS, ANDRÉ LUIS SOUZA D'AVILA-LEVY, CLAUDIA MASINI Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? |
title | Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? |
title_full | Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? |
title_fullStr | Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? |
title_full_unstemmed | Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? |
title_short | Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? |
title_sort | why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis? |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300003/ https://www.ncbi.nlm.nih.gov/pubmed/27869056 http://dx.doi.org/10.1017/S003118201600189X |
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