Mostrar el registro sencillo del ítem

dc.contributor.authorRoa Colomo, Amparo
dc.contributor.authorLópez Garrido, María Ángeles
dc.contributor.authorMolina Vallejo, María Pilar
dc.contributor.authorGonzález Sánchez, Mercedes
dc.contributor.authorAranda García, Violeta
dc.contributor.authorSalmerón Escobar, Francisco Javier 
dc.contributor.authorLorente Acosta, José Antonio 
dc.contributor.authorSerrano Fernández, María José 
dc.contributor.authorGarrido Navas, María del Carmen 
dc.date.accessioned2023-01-16T12:58:05Z
dc.date.available2023-01-16T12:58:05Z
dc.date.issued2022-11-28
dc.identifier.citationRoa-Colomo A... [et al.] (2022), Hepatocellular carcinoma riskstratification based on ASGR1 in circulating epithelial cells for cancer interception. Front. Mol. Biosci. 9:1074277. doi: [10.3389/fmolb.2022.1074277]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/79026
dc.description.abstractPurpose: Lack of diagnostic and prognostic biomarkers in hepatocellular carcinoma impedes stratifying patients based on their risk of developing cancer. The aim of this study was to evaluate phenotypic and genetic heterogeneity of circulating epithelial cells (CECs) based on asialoglycoprotein receptor 1 (ASGR1) and miR-122-5p expression as potential diagnostic and prognostic tools in patients with hepatocellular carcinoma (HCC) and liver cirrhosis (LC). Methods: Peripheral blood samples were extracted from LC and HCC patients at different disease stages. CECs were isolated using positive immunomagnetic selection. Genetic and phenotypic characterization was validated by double immunocytochemistry for cytokeratin (CK) and ASGR1 or by in situ hybridization with miR-122-5p and CECs were visualized by confocal microscopy. Results: The presence of CECs increased HCC risk by 2.58-fold, however, this was only significant for patients with previous LC (p = 0.028) and not for those without prior LC (p = 0.23). Furthermore, the number of CECs lacking ASGR1 expression correlated significantly with HCC incidence and absence of miR-122-5p expression (p = 0.014; r = 0.23). Finally, overall survival was significantly greater for patients at earlier cancer stages (p = 0.018), but this difference was only maintained in the group with the presence of CECs (p = 0.021) whereas progression-free survival was influenced by the absence of ASGR1 expression. Conclusion: Identification and characterization of CECs by ASGR1 and/or miR- 122-5p expression may be used as a risk-stratification tool in LC patients, as it was shown to be an independent prognostic and risk-stratification marker in LC and early disease stage HCC patients.es_ES
dc.description.sponsorshipRegional Ministry of Health of Andalusiaes_ES
dc.description.sponsorshipMinistry of Economy, Competitiveness, Enterprises and Universities PC-0522-2016 PC-0267-2017 PC-0033-2017es_ES
dc.description.sponsorshipHealth Institute Carlos III (ISCIII) DOC_01682 CD18/00126es_ES
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHepatocellular carcinomaes_ES
dc.subjectLiver cirrhosises_ES
dc.subjectCirculating tumor cellses_ES
dc.subjectPrecision medicinees_ES
dc.subjectCancer interceptiones_ES
dc.titleHepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interceptiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.3389/fmolb.2022.1074277
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


Ficheros en el ítem

[PDF]

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Atribución 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución 4.0 Internacional