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Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception

Purpose: 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 recep...

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Autores principales: Roa-Colomo, Amparo, López Garrido, María Ángeles, Molina-Vallejo, Pilar, Rojas, Angela, Sanchez, Mercedes González, Aranda-García, Violeta, Salmeron, Javier, Romero-Gomez, Manuel, Muntane, Jordi, Padillo, Javier, Alamo, Jose María, Lorente, Jose A., Serrano, María José, Garrido-Navas, M. Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742249/
https://www.ncbi.nlm.nih.gov/pubmed/36518850
http://dx.doi.org/10.3389/fmolb.2022.1074277
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author Roa-Colomo, Amparo
López Garrido, María Ángeles
Molina-Vallejo, Pilar
Rojas, Angela
Sanchez, Mercedes González
Aranda-García, Violeta
Salmeron, Javier
Romero-Gomez, Manuel
Muntane, Jordi
Padillo, Javier
Alamo, Jose María
Lorente, Jose A.
Serrano, María José
Garrido-Navas, M. Carmen
author_facet Roa-Colomo, Amparo
López Garrido, María Ángeles
Molina-Vallejo, Pilar
Rojas, Angela
Sanchez, Mercedes González
Aranda-García, Violeta
Salmeron, Javier
Romero-Gomez, Manuel
Muntane, Jordi
Padillo, Javier
Alamo, Jose María
Lorente, Jose A.
Serrano, María José
Garrido-Navas, M. Carmen
author_sort Roa-Colomo, Amparo
collection PubMed
description Purpose: 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.
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spelling pubmed-97422492022-12-13 Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception Roa-Colomo, Amparo López Garrido, María Ángeles Molina-Vallejo, Pilar Rojas, Angela Sanchez, Mercedes González Aranda-García, Violeta Salmeron, Javier Romero-Gomez, Manuel Muntane, Jordi Padillo, Javier Alamo, Jose María Lorente, Jose A. Serrano, María José Garrido-Navas, M. Carmen Front Mol Biosci Molecular Biosciences Purpose: 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. Frontiers Media S.A. 2022-11-28 /pmc/articles/PMC9742249/ /pubmed/36518850 http://dx.doi.org/10.3389/fmolb.2022.1074277 Text en Copyright © 2022 Roa-Colomo, López Garrido, Molina-Vallejo, Rojas, Sanchez, Aranda-García, Salmeron, Romero-Gomez, Muntane, Padillo, Alamo, Lorente, Serrano and Garrido-Navas. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Roa-Colomo, Amparo
López Garrido, María Ángeles
Molina-Vallejo, Pilar
Rojas, Angela
Sanchez, Mercedes González
Aranda-García, Violeta
Salmeron, Javier
Romero-Gomez, Manuel
Muntane, Jordi
Padillo, Javier
Alamo, Jose María
Lorente, Jose A.
Serrano, María José
Garrido-Navas, M. Carmen
Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception
title Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception
title_full Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception
title_fullStr Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception
title_full_unstemmed Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception
title_short Hepatocellular carcinoma risk-stratification based on ASGR1 in circulating epithelial cells for cancer interception
title_sort hepatocellular carcinoma risk-stratification based on asgr1 in circulating epithelial cells for cancer interception
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742249/
https://www.ncbi.nlm.nih.gov/pubmed/36518850
http://dx.doi.org/10.3389/fmolb.2022.1074277
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