BRAF V600E Detection in Liquid Biopsies from Pediatric Central Nervous System Tumors

dc.centroUniversidad San Pablo-CEU
dc.contributor.authorGarcía Romero, Noemí
dc.contributor.authorAyuso Sacido, Ángel
dc.contributor.authorCarrión-Navarro, Josefa
dc.contributor.authorAreal Hidalgo, María del Pilar
dc.contributor.authorAsensi-Puig, Adriá
dc.contributor.authorMadurga, Rodrigo
dc.contributor.authorNúñez-Torres, Rocio
dc.contributor.authorGonzález-Neira, Anna
dc.contributor.authorBelda Iniesta, Cristóbal
dc.contributor.authorGonzález Rumayor, Víctor
dc.contributor.authorLópez-Ibor Aliño, Blanca
dc.contributor.authorOrtiz de Mendivil Arrate, Ana
dc.contributor.otherGrupo: Spanish Back Pain Research Network (REIDE)
dc.date.accessioned2024-02-08T13:52:13Z
dc.date.available2024-02-08T13:52:13Z
dc.date.issued2019-12-25
dc.description.abstractPediatric Central Nervous System (CNS) tumors are the most fatal cancer diseases in childhood. Due to their localization and infiltrative nature, some tumor resections or biopsies are not feasible. In those cases, the use of minimally invasive methods as diagnostic, molecular marker detection, prognostic or monitoring therapies are emerging. The analysis of liquid biopsies which contain genetic information from the tumor has been much more widely explored in adults than in children. We compare the detection of BRAF V600E targetable mutation by digital-PCR from cell-free-DNA and EV-derived DNA (ctDNA) in serum, plasma and cerebrospinal fluid (CSF) isolated from a cohort of 29 CNS pediatric patients. Here we demonstrate that ctDNA isolated from serum and plasma could be successfully analyzed to obtain tumor genetic information which could be used to guide critical treatment decisions.en_EN
dc.formatapplication/pdf
dc.identifier.citationGarcía-Romero N, Carrión-Navarro J, Areal-Hidalgo P, Ortiz de Mendivil A, Asensi-Puig A, Madurga R, Núñez-Torres R, González-Neira A, Belda-Iniesta C, González-Rumayor V, López-Ibor B, Ayuso-Sacido A. BRAF V600E Detection in Liquid Biopsies from Pediatric Central Nervous System Tumors. Cancers (Basel). 2019 Dec 25;12(1):66. doi: 10.3390/cancers12010066.es_ES
dc.identifier.doi10.3390/cancers12010066
dc.identifier.issn2072-6694
dc.identifier.urihttp://hdl.handle.net/10637/15396
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofCancers
dc.relation.projectIDFunded by grants from the ‘Fondo de Investigaciones Sanitarias’ (FIS) (PI17-01489), the Miguel Servet Program (CP11/00147) del Instituto de Salud Carlos III (AAS), the Ministerio de Economía y Competitividad–FEDERER (RTC-2016-4990-1), Premio Fundación Mutua Madrileña XIII convocatoria, 2016, and Intheos Foundation.
dc.rightsopen access
dc.rights.cchttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subjectPediatric brain tumorsen_EN
dc.subjectLiquid biopsyen_EN
dc.subjectBRAFen_EN
dc.subjectDabrafeniben_EN
dc.titleBRAF V600E Detection in Liquid Biopsies from Pediatric Central Nervous System Tumorsen_EN
dc.typeArtículoes_ES
dspace.entity.typePublicationes
relation.isAuthorOfPublicationd62c35eb-39c5-4a3a-a292-ca764a4513bf
relation.isAuthorOfPublication128d29d8-a05b-456f-afa1-1bf8de84617e
relation.isAuthorOfPublication.latestForDiscoveryd62c35eb-39c5-4a3a-a292-ca764a4513bf

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