Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/104805
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dc.contributor.authorTrindade, Fábio-
dc.contributor.authorBarros, António Sousa-
dc.contributor.authorSilva, Jéssica-
dc.contributor.authorVlahou, Antonia-
dc.contributor.authorFalcão-Pires, Inês-
dc.contributor.authorGuedes, Sofia-
dc.contributor.authorVitorino, Carla-
dc.contributor.authorFerreira, Rita-
dc.contributor.authorLeite-Moreira, Adelino-
dc.contributor.authorAmado, Francisco-
dc.contributor.authorVitorino, Rui-
dc.date.accessioned2023-01-25T10:54:55Z-
dc.date.available2023-01-25T10:54:55Z-
dc.date.issued2021-05-31-
dc.identifier.issn1422-0067pt
dc.identifier.urihttps://hdl.handle.net/10316/104805-
dc.description.abstractNative biofluid peptides offer important information about diseases, holding promise as biomarkers. Particularly, the non-invasive nature of urine sampling, and its high peptide concentration, make urine peptidomics a useful strategy to study the pathogenesis of renal conditions. Moreover, the high number of detectable peptides as well as their specificity set the ground for the expansion of urine peptidomics to the identification of surrogate biomarkers for extra-renal diseases. Peptidomics further allows the prediction of proteases (degradomics), frequently dysregulated in disease, providing a complimentary source of information on disease pathogenesis and biomarkers. Then, what does urine peptidomics tell us so far? In this paper, we appraise the value of urine peptidomics in biomarker research through a comprehensive analysis of all datasets available to date. We have mined > 50 papers, addressing > 30 different conditions, comprising > 4700 unique peptides. Bioinformatic tools were used to reanalyze peptide profiles aiming at identifying disease fingerprints, to uncover hidden disease-specific peptides physicochemical properties and to predict the most active proteases associated with their generation. The molecular patterns found in this study may be further validated in the future as disease biomarker not only for kidney diseases but also for extra-renal conditions, as a step forward towards the implementation of a paradigm of predictive, preventive and personalized (3P) medicine.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationUIDB/IC/00051/2020pt
dc.relationUIDP/00051/2020pt
dc.relationUIDB/04501/2020pt
dc.relationPOCI- 01-0145-FEDER-007628pt
dc.relationUIDB/50006/2020pt
dc.relationPOCI-01-0145-FEDER-016385pt
dc.relationFCT - SAICTPAC/0047/2015pt
dc.relationIF/00286/2015pt
dc.relationUIDP/00051/2020pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjecturinept
dc.subjectpeptidespt
dc.subjectproteasespt
dc.subjectpeptidomicspt
dc.subjectdegradomicspt
dc.subjectbiomarkerspt
dc.subjectpredictive, preventive and personalized (3P) medicinept
dc.subjectmolecular patternspt
dc.subjectindividualized patient profilingpt
dc.subject.meshBiomarkerspt
dc.subject.meshHumanspt
dc.subject.meshPeptidespt
dc.subject.meshProteomept
dc.subject.meshUrinept
dc.titleMining the Biomarker Potential of the Urine Peptidome: From Amino Acids Properties to Proteasespt
dc.typearticle-
degois.publication.firstPage5940pt
degois.publication.issue11pt
degois.publication.titleInternational Journal of Molecular Sciencespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/ijms22115940pt
degois.publication.volume22pt
dc.date.embargo2021-05-31*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-9103-5852-
crisitem.author.orcid0000-0003-3424-548X-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
I&D CQC - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
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