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Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma
BACKGROUND AND AIM: The epithelial cell adhesion molecule (EpCAM) has been proposed as a marker for cancer stem cells in human hepatocellular carcinoma (HCC) as well as in the development of novel target therapies. This study aimed to investigate the immunohistochemical expression of EpCAM and alpha...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077358/ https://www.ncbi.nlm.nih.gov/pubmed/30112355 http://dx.doi.org/10.1155/2018/5970852 |
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author | Lima, Leonardo do Prado Machado, Carla Jorge Rodrigues, João Bernardo Sancio Rocha Vasconcellos, Leonardo de Souza Junior, Eduardo Paulino Vidigal, Paula Vieira Teixeira Resende, Vivian |
author_facet | Lima, Leonardo do Prado Machado, Carla Jorge Rodrigues, João Bernardo Sancio Rocha Vasconcellos, Leonardo de Souza Junior, Eduardo Paulino Vidigal, Paula Vieira Teixeira Resende, Vivian |
author_sort | Lima, Leonardo do Prado |
collection | PubMed |
description | BACKGROUND AND AIM: The epithelial cell adhesion molecule (EpCAM) has been proposed as a marker for cancer stem cells in human hepatocellular carcinoma (HCC) as well as in the development of novel target therapies. This study aimed to investigate the immunohistochemical expression of EpCAM and alpha-fetoprotein (AFP) in HCC patients and their association with clinicopathological characteristics. METHODS: This study included Child-Pugh A HCC patients undergoing curative surgical resection. RESULTS: A significant difference was observed in the ratio between the different phenotypes (p = 0.002), identifying 12 (29.3%) EPCAM positive tumors and 29 (70.7%) negative tumors. EpCAM+ expression was associated with AFP + (OR = 12.5, 95% CI, 1.9-84.1, p<0.001). In univariate analysis, a significant association was observed between AFP+ and EPCAM+ and the serum AFP level. A diameter of ≤ 5 cm was associated with EPCAM+, while angiolymphatic invasion was associated with APF+. In a multivariate analysis, only tumors of ≤ 5 cm were significantly associated with EpCAM+ (OR = 8.7; 95%CI, 1.27-100.0; p = 0.022). The overall survival rate was 74.9%, 69.4%, 69.4%, and 53.5% at 12, 24, 36, and 48 months, respectively. CONCLUSION: A considerable number of patients with EpCAM+ HCC would benefit from a specific target therapy. |
format | Online Article Text |
id | pubmed-6077358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60773582018-08-15 Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma Lima, Leonardo do Prado Machado, Carla Jorge Rodrigues, João Bernardo Sancio Rocha Vasconcellos, Leonardo de Souza Junior, Eduardo Paulino Vidigal, Paula Vieira Teixeira Resende, Vivian Can J Gastroenterol Hepatol Research Article BACKGROUND AND AIM: The epithelial cell adhesion molecule (EpCAM) has been proposed as a marker for cancer stem cells in human hepatocellular carcinoma (HCC) as well as in the development of novel target therapies. This study aimed to investigate the immunohistochemical expression of EpCAM and alpha-fetoprotein (AFP) in HCC patients and their association with clinicopathological characteristics. METHODS: This study included Child-Pugh A HCC patients undergoing curative surgical resection. RESULTS: A significant difference was observed in the ratio between the different phenotypes (p = 0.002), identifying 12 (29.3%) EPCAM positive tumors and 29 (70.7%) negative tumors. EpCAM+ expression was associated with AFP + (OR = 12.5, 95% CI, 1.9-84.1, p<0.001). In univariate analysis, a significant association was observed between AFP+ and EPCAM+ and the serum AFP level. A diameter of ≤ 5 cm was associated with EPCAM+, while angiolymphatic invasion was associated with APF+. In a multivariate analysis, only tumors of ≤ 5 cm were significantly associated with EpCAM+ (OR = 8.7; 95%CI, 1.27-100.0; p = 0.022). The overall survival rate was 74.9%, 69.4%, 69.4%, and 53.5% at 12, 24, 36, and 48 months, respectively. CONCLUSION: A considerable number of patients with EpCAM+ HCC would benefit from a specific target therapy. Hindawi 2018-07-19 /pmc/articles/PMC6077358/ /pubmed/30112355 http://dx.doi.org/10.1155/2018/5970852 Text en Copyright © 2018 Leonardo do Prado Lima et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lima, Leonardo do Prado Machado, Carla Jorge Rodrigues, João Bernardo Sancio Rocha Vasconcellos, Leonardo de Souza Junior, Eduardo Paulino Vidigal, Paula Vieira Teixeira Resende, Vivian Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma |
title | Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma |
title_full | Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma |
title_fullStr | Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma |
title_full_unstemmed | Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma |
title_short | Immunohistochemical Coexpression of Epithelial Cell Adhesion Molecule and Alpha-Fetoprotein in Hepatocellular Carcinoma |
title_sort | immunohistochemical coexpression of epithelial cell adhesion molecule and alpha-fetoprotein in hepatocellular carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077358/ https://www.ncbi.nlm.nih.gov/pubmed/30112355 http://dx.doi.org/10.1155/2018/5970852 |
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