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dc.contributor.authorFernández Lázaro, Diego 
dc.contributor.authorGarrosa, Evelina
dc.contributor.authorSeco Calvo, Jesús
dc.contributor.authorGarrosa García, Manuel 
dc.date.accessioned2023-08-25T08:36:32Z
dc.date.available2023-08-25T08:36:32Z
dc.date.issued2022
dc.identifier.citationProteomes, 2022, Vol. 10, Nº. 3, 29es
dc.identifier.issn2227-7382es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/61098
dc.descriptionProducción Científicaes
dc.description.abstractSarcopenia (Sp) is the loss of skeletal muscle mass associated with aging which causes an involution of muscle function and strength. Satellite cells (Sc) are myogenic stem cells, which are activated by injury or stress, and repair muscle tissue. With advancing age, there is a decrease in the efficiency of the regenerative response of Sc. Diagnosis occurs with the Sp established by direct assessments of muscle. However, the detection of biomarkers in real-time biofluids by liquid biopsy could represent a step-change in the understanding of the molecular biology and heterogeneity of Sp. A total of 13 potential proteogenomic biomarkers of Sp by their physiological and biological interaction with Sc have been previously described in the literature. Increases in the expression of GDF11, PGC-1α, Sirt1, Pax7, Pax3, Myf5, MyoD, CD34, MyoG, and activation of Notch signaling stimulate Sc activity and proliferation, which could modulate and delay Sp progression. On the contrary, intensified expression of GDF8, p16INK4a, Mrf4, and activation of the Wnt pathway would contribute to early Sp development by directly inducing reduced and/or altered Sc function, which would attenuate the restorative capacity of skeletal muscle. Additionally, tissue biopsy remains an important diagnostic tool. Proteomic profiling of aged muscle tissues has shown shifts toward protein isoforms characteristic of a fast-to-slow transition process and an elevated number of oxidized proteins. In addition, a strong association between age and plasma values of growth differentiation factor 15 (GDF-15) has been described and serpin family A member 3 (serpin A3n) was more secreted by atrophied muscle cells. The identification of these new biomarkers holds the potential to change personalized medicine because it could predict in real time the course of Sp by monitoring its evolution and assessing responses to potential therapeutic strategies.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherMDPIes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectMuscles - Diseaseses
dc.subjectMúsculos - Enfermedadeses
dc.subjectMuscles - Aginges
dc.subjectMúsculos - Envejecimientoes
dc.subjectMusculoskeletal diseases in old agees
dc.subjectMuscular atrophyes
dc.subjectAtrofia musculares
dc.subjectProteomicses
dc.subjectProteomicaes
dc.subjectMedical geneticses
dc.subjectMuscles - Biopsyes
dc.subjectCell Biologyes
dc.subjectAginges
dc.subjectEnvejecimientoes
dc.subjectBiomarkerses
dc.titlePotential satellite cell-linked biomarkers in aging skeletal muscle tissue: Proteomics and proteogenomics to monitor sarcopeniaes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2022 The Authorses
dc.identifier.doi10.3390/proteomes10030029es
dc.relation.publisherversionhttps://www.mdpi.com/2227-7382/10/3/29es
dc.identifier.publicationfirstpage29es
dc.identifier.publicationissue3es
dc.identifier.publicationtitleProteomeses
dc.identifier.publicationvolume10es
dc.peerreviewedSIes
dc.identifier.essn2227-7382es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco3201.02 Genética Clínicaes
dc.subject.unesco2407 Biología Celulares


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