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dc.contributor.authorJiménez Luna, Cristina 
dc.contributor.authorGonzález Flores, Encarnación
dc.contributor.authorOrtiz Quesada, Raúl 
dc.contributor.authorMartínez González, Luis Javier 
dc.contributor.authorAntúnez Rodríguez, Alba
dc.contributor.authorExpósito Ruiz, Manuela 
dc.contributor.authorMelguizo Alonso, Consolación 
dc.contributor.authorCaba Pérez, Octavio 
dc.contributor.authorPrados Salazar, José Carlos 
dc.date.accessioned2021-05-25T12:30:06Z
dc.date.available2021-05-25T12:30:06Z
dc.date.issued2021
dc.identifier.citationJimenez-Luna, C.; González-Flores, E.; Ortiz, R.; Martínez-González, L.J.; Antúnez-Rodríguez, A.; Expósito-Ruiz, M.; Melguizo, C.; Caba, O.; Prados, J. Circulating PTGS2, JAG1, GUCY2C and PGF mRNA in Peripheral Blood and Serum as Potential Biomarkers for Patients with Metastatic Colon Cancer. J. Clin. Med. 2021, 10, 2248. https://doi.org/10.3390/jcm10112248es_ES
dc.identifier.urihttp://hdl.handle.net/10481/68721
dc.description.abstractGenes involved in the angiogenic process have been proposed for the diagnosis and therapeutic response of metastatic colorectal cancer (CRC). This study aimed to investigate the value of PTGS2, JAG1, GUCY2C and PGF-circulating RNA as biomarkers in metastatic CRC. Blood cells and serum mRNA from 59 patients with metastatic CRC and 47 healthy controls were analyzed by digital PCR. The area under the receiver operating characteristic curve (AUC) was used to estimate the diagnostic value of each mRNA alone or mRNA combinations. A significant upregulation of the JAG1, PTGS2 and GUCY2C genes in blood cells and serum samples from metastatic CRC patients was detected. Circulating mRNA levels in the serum of all genes were significantly more abundant than in blood. The highest discrimination ability between metastatic CRC patients and healthy donors was obtained with PTGS2 (AUC of 0.984) and GUCY2C (AUC of 0.896) in serum samples. Biomarker combinations did not improve the discriminatory capacity of biomarkers separately. Analyzed biomarkers showed no correlation with overall survival or progression-free survival, but GUCY2C and GUCY2C/PTGS2 expression in serum correlated significantly with the response to antiangiogenic agents. These findings demonstrate that assessment of genes involved in the angiogenic process may be a potential non-invasive diagnostic tool for metastatic CRC and its response to antiangiogenic therapy.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII) (Project PI19/01478) (FEDER) and by the CTS-107 Groupes_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectMetastatic colon canceres_ES
dc.subjectBiomarkerses_ES
dc.subjectAngiogenesises_ES
dc.subjectLiquid biopsieses_ES
dc.subjectCirculating mRNAes_ES
dc.subjectDigital PCRes_ES
dc.titleCirculating PTGS2, JAG1, GUCY2C and PGF mRNA in Peripheral Blood and Serum as Potential Biomarkers for Patients with Metastatic Colon Canceres_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/jcm10112248


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