dc.creatorMartínez Sayé, Melisa Soledad
dc.creatorReigada, Chantal
dc.creatorGauna, Lucrecia Antonella
dc.creatorValera Vera, Edward Augusto
dc.creatorPereira, Claudio Alejandro
dc.creatorMiranda, Mariana Reneé
dc.date.accessioned2020-05-18T16:31:13Z
dc.date.accessioned2022-10-15T02:34:17Z
dc.date.available2020-05-18T16:31:13Z
dc.date.available2022-10-15T02:34:17Z
dc.date.created2020-05-18T16:31:13Z
dc.date.issued2019-12
dc.identifierMartínez Sayé, Melisa Soledad; Reigada, Chantal; Gauna, Lucrecia Antonella; Valera Vera, Edward Augusto; Pereira, Claudio Alejandro; et al.; Amino acid and polyamine membrane transporters in Trypanosoma cruzi: biological function and evaluation as drug targets; Bentham Science Publishers; Current Medicinal Chemistry; 26; 36; 12-2019; 6636-6651
dc.identifier0929-8673
dc.identifierhttp://hdl.handle.net/11336/105349
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4335651
dc.description.abstractAmino acids and polyamines are involved in relevant processes for the parasite Trypanosoma cruzi, like protein synthesis, stress resistance, life cycle progression, infection establishment and redox balance, among others. In addition to the biosynthetic routes of amino acids, T. cruzi possesses transport systems that allow the active uptake from the extracellular medium; and in the case of polyamines, the uptake is the unique way to obtain these compounds. The TcAAAP protein family is absent in mammals and its members are responsible for amino acid and derivative uptake, thus the TcAAAP permeases are not only interesting and promising therapeutic targets but also could be used to direct the entry of toxic compounds into the parasite.Although there is a treatment available for Chagas disease, its limited efficacy in the chronic stage of the disease, as well as the side effects reported, highlight the urgent need to develop new therapies. Discovery of new drugs is a slow and money-consuming process, and even during clinical trials the drugs can fail. In this context, drug repositioning is an interesting and recommended strategy by the World Health Organization since costs and time are significantly reduced. In this article, amino acids and polyamines transport and its potential as therapeutic targets will be revised, including examples of synthetic drugs and drug repurposing.
dc.languageeng
dc.publisherBentham Science Publishers
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.eurekaselect.com/172842/article
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.2174/0929867326666190620094710
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectTRYPANOSOMA CRUZI
dc.subjectAMINO ACID TRANSPORT
dc.subjectPOLYAMINE TRANSPORT
dc.subjectTHERAPEUTIC TARGET
dc.subjectDRUG DISCOVERY
dc.subjectDRUG REPOSITIONING
dc.subjectNEW THERAPIES
dc.subjectCHAGAS DISEASE
dc.titleAmino acid and polyamine membrane transporters in Trypanosoma cruzi: biological function and evaluation as drug targets
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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