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dc.contributor.authorEspejo-Cruz, María Lola
dc.contributor.authorGonzález Rubio, Sandra
dc.contributor.authorEspejo, Juan J.
dc.contributor.authorZamora-Olaya, Javier
dc.contributor.authorAlejandre, Rafael
dc.contributor.authorPrieto-Torre, María
dc.contributor.authorLinares Luna, Clara Isabel
dc.contributor.authorGuerrero-Misas, Marta
dc.contributor.authorBarrera-Baena, Pilar
dc.contributor.authorPoyato-González, Antonio
dc.contributor.authorSánchez-Frías, Marina
dc.contributor.authorAyllón Terán, M. Dolores
dc.contributor.authorRodríguez-Perálvarez, Manuel
dc.contributor.authorMata, Manuel de la
dc.contributor.authorFerrín, Gustavo
dc.date.accessioned2023-01-31T13:06:21Z
dc.date.available2023-01-31T13:06:21Z
dc.date.issued2023
dc.identifier.urihttp://hdl.handle.net/10396/24589
dc.description.abstractCirculating tumor cells (CTCs), and particularly circulating cancer stem cells (cCSC), are prognostic biomarkers for different malignancies and may be detected using liquid biopsies. The ex vivo culture of cCSCs would provide valuable information regarding biological aggressiveness and would allow monitoring the adaptive changes acquired by the tumor in real time. In this prospective pilot study, we analyzed the presence of EpCAM+ CTCs using the IsoFlux system in the peripheral blood of 37 patients with hepatocellular carcinoma undergoing transarterial chemoembolization (TACE). The average patient age was 63.5 ± 7.9 years and 91.9% of the patients were men. All patients had detectable CTCs at baseline and 20 patients (54.1%) showed CTC aggregates or clusters in their peripheral blood. The increased total tumor diameter (OR: 2.5 (95% CI: 1.3–4.8), p = 0.006) and the absence of clusters of CTCs at baseline (OR: 0.2 (95% CI: 0.0–1.0), p = 0.049) were independent predictors of a diminished response to TACE. Culture of cCSC was successful in five out of thirty-three patients, mostly using negative enrichment of CD45− cells, ultra-low adherence, high glucose, and a short period of hypoxia followed by normoxia. In conclusion, the identification of clusters of CTCs before TACE and the implementation of standardized approaches for cCSC culture could aid to predict outcomes and to define the optimal adjuvant therapeutic strategy for a true personalized medicine in hepatocellular carcinoma.es_ES
dc.format.mimetypeapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightshttps://creativecommons.org/licenses/by/4.0/es_ES
dc.sourceInternational Journal of Molecular Science, 24(3), 2558 (2023)es_ES
dc.subjectCirculating tumor cellses_ES
dc.subjectCirculating cancer stem cellses_ES
dc.subjectLiquid biopsyes_ES
dc.subjectHepatocellular carcinomaes_ES
dc.subjectTransarterial chemoembolizationes_ES
dc.subjectSpheroidses_ES
dc.titleEnumeration and Characterization of Circulating Tumor Cells in Patients with Hepatocellular Carcinoma Undergoing Transarterial Chemoembolizationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.3390/ijms24032558es_ES
dc.relation.projectIDGobierno de España. PI18/01736 (FEDER)es_ES
dc.relation.projectIDJunta de Andalucía. RH-0075-2020 (FEDER)es_ES
dc.relation.projectIDJunta de Andalucía. RH-0010-2021 (FEDER)es_ES
dc.relation.projectIDGobierno de España. FI19/00357es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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