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Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress
Despite the increasing number of manuscripts describing potential alternative antileishmanial compounds, little is advancing on translating these knowledges to new products to treat leishmaniasis. This is in part due to the lack of standardisations during pre-clinical drug discovery stage and also d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto Oswaldo Cruz, Ministério da Saúde
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944189/ https://www.ncbi.nlm.nih.gov/pubmed/35320824 http://dx.doi.org/10.1590/0074-02760220403 |
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author | do Monte, Rubens Lima Moreira, Paulo Otávio Lourenço de Sousa, Alessandra Mara Garcia, Miguel Antonio do Nascimento Maran, Suellen Rodrigues Moretti, Nilmar Silvio |
author_facet | do Monte, Rubens Lima Moreira, Paulo Otávio Lourenço de Sousa, Alessandra Mara Garcia, Miguel Antonio do Nascimento Maran, Suellen Rodrigues Moretti, Nilmar Silvio |
author_sort | do Monte, Rubens Lima |
collection | PubMed |
description | Despite the increasing number of manuscripts describing potential alternative antileishmanial compounds, little is advancing on translating these knowledges to new products to treat leishmaniasis. This is in part due to the lack of standardisations during pre-clinical drug discovery stage and also depends on the alignment of goals among universities/research centers, government and pharmaceutical industry. Inspired or not by drug repurposing, metal-based antileishmanial drugs represent a class that deserves more attention on its use for leishmaniasis chemotherapy. Together with new chemical entities, progresses have been made on the knowledge of parasite-specific drug targets specially after using CRISPR/Cas system for functional studies. In this regard, Leishmania parasites undergoe post-translational modification as key regulators in several cellular processes, which represents an entire new field for drug target elucidation, once this is poorly explored. This perspective review describes the advances on antileishmanial metallodrugs and the elucidation of drug targets based on post-translational modifications, highlighting the limitations on the drug discovery/development process and suggesting standardisations focused on products addressed to who need it most. |
format | Online Article Text |
id | pubmed-8944189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Instituto Oswaldo Cruz, Ministério da Saúde |
record_format | MEDLINE/PubMed |
spelling | pubmed-89441892022-04-08 Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress do Monte, Rubens Lima Moreira, Paulo Otávio Lourenço de Sousa, Alessandra Mara Garcia, Miguel Antonio do Nascimento Maran, Suellen Rodrigues Moretti, Nilmar Silvio Mem Inst Oswaldo Cruz Perspective Despite the increasing number of manuscripts describing potential alternative antileishmanial compounds, little is advancing on translating these knowledges to new products to treat leishmaniasis. This is in part due to the lack of standardisations during pre-clinical drug discovery stage and also depends on the alignment of goals among universities/research centers, government and pharmaceutical industry. Inspired or not by drug repurposing, metal-based antileishmanial drugs represent a class that deserves more attention on its use for leishmaniasis chemotherapy. Together with new chemical entities, progresses have been made on the knowledge of parasite-specific drug targets specially after using CRISPR/Cas system for functional studies. In this regard, Leishmania parasites undergoe post-translational modification as key regulators in several cellular processes, which represents an entire new field for drug target elucidation, once this is poorly explored. This perspective review describes the advances on antileishmanial metallodrugs and the elucidation of drug targets based on post-translational modifications, highlighting the limitations on the drug discovery/development process and suggesting standardisations focused on products addressed to who need it most. Instituto Oswaldo Cruz, Ministério da Saúde 2022-03-23 /pmc/articles/PMC8944189/ /pubmed/35320824 http://dx.doi.org/10.1590/0074-02760220403 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License |
spellingShingle | Perspective do Monte, Rubens Lima Moreira, Paulo Otávio Lourenço de Sousa, Alessandra Mara Garcia, Miguel Antonio do Nascimento Maran, Suellen Rodrigues Moretti, Nilmar Silvio Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress |
title | Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress |
title_full | Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress |
title_fullStr | Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress |
title_full_unstemmed | Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress |
title_short | Antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress |
title_sort | antileishmanial metallodrugs and the elucidation of new drug targets linked to post-translational modifications machinery: pitfalls and progress |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944189/ https://www.ncbi.nlm.nih.gov/pubmed/35320824 http://dx.doi.org/10.1590/0074-02760220403 |
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