Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.

Introduction: Trypanosoma cruzi, Trypanosoma brucei, and Leishmania spp., commonly referred to as TriTryps, are a group of protozoan parasites that cause important human diseases affecting millions of people belonging to the most vulnerable populations worldwide. Current treatments have limited effi...

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Main Author: Rivara-Espasandín, Martín (author)
Other Authors: Palumbo, Miranda Clara (author), Sosa, Ezequiel J. (author), Radío, Santiago (author), Turjanski, Adrián G. (author), Sotelo-Silveira, José Roberto (author), Fernández Do Porto, Dario (author), Smircich, Pablo (author)
Format: article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/20.500.12008/43273
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author Rivara-Espasandín, Martín
author2 Palumbo, Miranda Clara
Sosa, Ezequiel J.
Radío, Santiago
Turjanski, Adrián G.
Sotelo-Silveira, José Roberto
Fernández Do Porto, Dario
Smircich, Pablo
author2_role author
author
author
author
author
author
author
author_browse Fernández Do Porto, Dario
Palumbo, Miranda Clara
Radío, Santiago
Rivara-Espasandín, Martín
Smircich, Pablo
Sosa, Ezequiel J.
Sotelo-Silveira, José Roberto
Turjanski, Adrián G.
author_facet Rivara-Espasandín, Martín
Palumbo, Miranda Clara
Sosa, Ezequiel J.
Radío, Santiago
Turjanski, Adrián G.
Sotelo-Silveira, José Roberto
Fernández Do Porto, Dario
Smircich, Pablo
author_role author
collection COLIBRI
dc.contributor.none.fl_str_mv Rivara-Espasandín Martín, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.
Palumbo Miranda Clara
Sosa Ezequiel J.
Radío Santiago, IIBCE
Turjanski Adrián G.
Sotelo-Silveira José Roberto, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.
Fernández Do Porto Dario
Smircich Pablo, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.
dc.creator.none.fl_str_mv Rivara-Espasandín, Martín
Palumbo, Miranda Clara
Sosa, Ezequiel J.
Radío, Santiago
Turjanski, Adrián G.
Sotelo-Silveira, José Roberto
Fernández Do Porto, Dario
Smircich, Pablo
dc.date.none.fl_str_mv 2023
2024-04-01T13:38:12Z
2024-04-01T13:38:12Z
dc.format.none.fl_str_mv 10 h.
application/pdf
dc.identifier.none.fl_str_mv Rivara-Espasandín, M, Palumbo, M, Sosa, E y otros. "Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections". Frontiers in Pharmacology. [en línea] 2023, 14: 1136321. 10 h. DOI: 10.3389/fphar.2023.1136321.
1663-9812
https://hdl.handle.net/20.500.12008/43273
10.3389/fphar.2023.1136321
dc.language.none.fl_str_mv en
eng
dc.publisher.none.fl_str_mv Frontiers
dc.relation.none.fl_str_mv Frontiers in Pharmacology, 2023, 14: 1136321.
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
Licencia Creative Commons Atribución (CC - By 4.0)
dc.source.none.fl_str_mv reponame:COLIBRI
instname:Universidad de la República
instacron:Universidad de la República
dc.subject.none.fl_str_mv Trypanosomatids
Drug discovery
Genomics
Neglected disease
Target selection
dc.title.none.fl_str_mv Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
dc.type.none.fl_str_mv Artículo
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
description Introduction: Trypanosoma cruzi, Trypanosoma brucei, and Leishmania spp., commonly referred to as TriTryps, are a group of protozoan parasites that cause important human diseases affecting millions of people belonging to the most vulnerable populations worldwide. Current treatments have limited efficiencies and can cause serious side effects, so there is an urgent need to develop new control strategies. Presently, the identification and prioritization of appropriate targets can be aided by integrative genomic and computational approaches. Methods: In this work, we conducted a genome-wide multidimensional data integration strategy to prioritize drug targets. We included genomic, transcriptomic, metabolic, and protein structural data sources, to delineate candidate proteins with relevant features for target selection in drug development. Results and Discussion: Our final ranked list includes proteins shared by TriTryps and covers a range of biological functions including essential proteins for parasite survival or growth, oxidative stress-related enzymes, virulence factors, and proteins that are exclusive to these parasites. Our strategy found previously described candidates, which validates our approach as well as new proteins that can be attractive targets to consider during the initial steps of drug discovery
eu_rights_str_mv openAccess
format article
id anni_e41f2f742e2a9969781931bedd41b8e9
identifier_str_mv Rivara-Espasandín, M, Palumbo, M, Sosa, E y otros. "Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections". Frontiers in Pharmacology. [en línea] 2023, 14: 1136321. 10 h. DOI: 10.3389/fphar.2023.1136321.
1663-9812
10.3389/fphar.2023.1136321
instacron_str Universidad de la República
institution Universidad de la República
instname_str Universidad de la República
language eng
language_invalid_str_mv en
network_acronym_str anni
network_name_str oai-lr-anni
oai_identifier_str oai:colibri.udelar.edu.uy:20.500.12008/43273
publishDate 2023
publishDateSort 2023
publisher.none.fl_str_mv Frontiers
reponame_str COLIBRI
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv Licencia Creative Commons Atribución (CC - By 4.0)
spelling Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.Rivara-Espasandín, MartínPalumbo, Miranda ClaraSosa, Ezequiel J.Radío, SantiagoTurjanski, Adrián G.Sotelo-Silveira, José RobertoFernández Do Porto, DarioSmircich, PabloTrypanosomatidsDrug discoveryGenomicsNeglected diseaseTarget selectionIntroduction: Trypanosoma cruzi, Trypanosoma brucei, and Leishmania spp., commonly referred to as TriTryps, are a group of protozoan parasites that cause important human diseases affecting millions of people belonging to the most vulnerable populations worldwide. Current treatments have limited efficiencies and can cause serious side effects, so there is an urgent need to develop new control strategies. Presently, the identification and prioritization of appropriate targets can be aided by integrative genomic and computational approaches. Methods: In this work, we conducted a genome-wide multidimensional data integration strategy to prioritize drug targets. We included genomic, transcriptomic, metabolic, and protein structural data sources, to delineate candidate proteins with relevant features for target selection in drug development. Results and Discussion: Our final ranked list includes proteins shared by TriTryps and covers a range of biological functions including essential proteins for parasite survival or growth, oxidative stress-related enzymes, virulence factors, and proteins that are exclusive to these parasites. Our strategy found previously described candidates, which validates our approach as well as new proteins that can be attractive targets to consider during the initial steps of drug discoveryFrontiersRivara-Espasandín Martín, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.Palumbo Miranda ClaraSosa Ezequiel J.Radío Santiago, IIBCETurjanski Adrián G.Sotelo-Silveira José Roberto, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.Fernández Do Porto DarioSmircich Pablo, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.2024-04-01T13:38:12Z2024-04-01T13:38:12Z2023Artículoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion10 h.application/pdfRivara-Espasandín, M, Palumbo, M, Sosa, E y otros. "Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections". Frontiers in Pharmacology. [en línea] 2023, 14: 1136321. 10 h. DOI: 10.3389/fphar.2023.1136321.1663-9812https://hdl.handle.net/20.500.12008/4327310.3389/fphar.2023.1136321reponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaenengFrontiers in Pharmacology, 2023, 14: 1136321.Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)info:eu-repo/semantics/openAccessLicencia Creative Commons Atribución (CC - By 4.0)oai:colibri.udelar.edu.uy:20.500.12008/432732026-04-14T10:10:35Z
spellingShingle Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
Rivara-Espasandín, Martín
Trypanosomatids
Drug discovery
Genomics
Neglected disease
Target selection
status_str publishedVersion
title Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
title_full Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
title_fullStr Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
title_full_unstemmed Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
title_short Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
title_sort Omics data integration facilitates target selection for new antiparasitic drugs against TriTryp infections.
topic Trypanosomatids
Drug discovery
Genomics
Neglected disease
Target selection
url https://hdl.handle.net/20.500.12008/43273