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dc.contributor.authorArance, Elena
dc.contributor.authorRamírez, Viviana
dc.contributor.authorRubio Roldán, Alejandro
dc.contributor.authorOcaña Peinado, Francisco 
dc.contributor.authorRomero Cachinero, Catalina
dc.contributor.authorJódar Reyes, Ana Belén 
dc.contributor.authorVázquez Alonso, Fernando
dc.contributor.authorMartínez González, Luis Javier 
dc.contributor.authorÁlvarez Cubero, María Jesús 
dc.date.accessioned2022-02-02T09:29:38Z
dc.date.available2022-02-02T09:29:38Z
dc.date.issued2021-12-31
dc.identifier.citationArance, E... [et al.]. Determination of Exosome Mitochondrial DNA as a Biomarker of Renal Cancer Aggressiveness. Cancers 2022, 14, 199. [https://doi.org/10.3390/cancers14010199]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/72607
dc.descriptionThis study is partially supported by ID#53169721 project funded by Pfizer and the exosomes characterization was financed thanks to the grant PY20_00241 (FEDER/Junta de Andalucia-Regional Ministry of Economic Transformation, Industry, Knowledge and Universities).es_ES
dc.description.abstractHere, the role of non-invasive biomarkers in liquid biopsy was evaluated, mainly in exosomes and mitochondrial DNA (mtDNA) as promising, novel, and stable biomarkers for renal cell carcinoma (RCC). A total of 140 fractions (named from B to F) obtained by ultracentrifugations of whole blood samples from 28 individuals (13 patients and 15 controls) were included. Nanoparticle Tracking Analysis (NTA) was conducted to characterized exosomal fraction. Subsequently, an analysis of digital PCR (dPCR) using the QuantStudio (TM) 3D Digital PCR platform was performed and the quantification of mtDNA copy number by QuantStudioTM 12K Flex Real-Time PCR System (qPCR) was developed. Moreover, Next Generation Sequencing (NGS) analyses were included using MiSeq system (Illumina, San Diego, CA, USA). An F fraction, which contains all exosome data and all mitochondrial markers, was identified in dPCR and qPCR with statistically significant power (adjusted p values <= 0.03) when comparing cases and controls. Moreover, present analysis in mtDNA showed a relevant significance in RCC aggressiveness. To sum up, this is the first time a relation between exosomal mtDNA markers and clinical management of RCC is analyzed. We suggest a promising strategy for future liquid biopsy RCC analysis, although more analysis should be performed prior to application in routine clinical practice.es_ES
dc.description.sponsorshipPfizer 53169721es_ES
dc.description.sponsorshipFEDER/Junta de Andalucia-Regional Ministry of Economic Transformation, Industry, Knowledge and Universities PY20_00241es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectBiomarkeres_ES
dc.subjectExtracellular vesicleses_ES
dc.subjectExosomees_ES
dc.subjectMitochondrial DNAes_ES
dc.subjectRenal canceres_ES
dc.titleDetermination of Exosome Mitochondrial DNA as a Biomarker of Renal Cancer Aggressivenesses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/cancers14010199
dc.type.hasVersionVoRes_ES


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