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The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors
INTRODUCTION: In the work up of primary solid liver lesions it is essential to differentiate correctly between benign and malignant tumors, such as hepatocellular adenoma (HCA) and hepatocellular carcinoma (HCC) respectively. A promising new marker to detect HCC is Golgi Protein 73 (GP73). Studies c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102481/ https://www.ncbi.nlm.nih.gov/pubmed/25033446 http://dx.doi.org/10.1371/journal.pone.0100187 |
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author | Bröker, Mirelle E. E. Ijzermans, Jan N. M. Witjes, Caroline D. M. van Vuuren, Hanneke J. de Man, Robert A. |
author_facet | Bröker, Mirelle E. E. Ijzermans, Jan N. M. Witjes, Caroline D. M. van Vuuren, Hanneke J. de Man, Robert A. |
author_sort | Bröker, Mirelle E. E. |
collection | PubMed |
description | INTRODUCTION: In the work up of primary solid liver lesions it is essential to differentiate correctly between benign and malignant tumors, such as hepatocellular adenoma (HCA) and hepatocellular carcinoma (HCC) respectively. A promising new marker to detect HCC is Golgi Protein 73 (GP73). Studies comparing patients with HCC and cirrhosis with normal controls suggested that GP73 is specific for patients with HCC; however, patients with other liver tumors were not included. We therefore studied the predictive value of GP73 in differentiating between solid benign and malignant liver tumors. MATERIALS AND METHODS: This study included 264 patients: 88 patients with HCC, 88 with hepatocellular adenoma (HCA), and 88 with focal nodal hyperplasia (FNH). A blood sample was collected from each patient to measure GP73 levels using a quantitative ELISA assay and differences in outcome between subgroups were compared. The receiver operating characteristic (ROC) curve, sensitivity and specificity of GP73 were calculated and compared to alpha-fetoprotein (AFP) levels. RESULTS: When comparing malignant and benign liver tumors the area under ROC was 0.701 and 0.912 for GP73 and AFP respectively. Test characteristics revealed a sensitivity of 60% for GP73 and 65% for AFP; in addition the specificity was 77% for GP73 and 96% for AFP. CONCLUSION: Although the literature suggests that GP73 is a valuable serum marker in patients with HCC, the serum concentration may also be increased in patients with solid benign liver tumors. Therefore, a GP73 assay is less suitable for discriminating between primary malignant and benign tumors of the liver. |
format | Online Article Text |
id | pubmed-4102481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41024812014-07-21 The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors Bröker, Mirelle E. E. Ijzermans, Jan N. M. Witjes, Caroline D. M. van Vuuren, Hanneke J. de Man, Robert A. PLoS One Research Article INTRODUCTION: In the work up of primary solid liver lesions it is essential to differentiate correctly between benign and malignant tumors, such as hepatocellular adenoma (HCA) and hepatocellular carcinoma (HCC) respectively. A promising new marker to detect HCC is Golgi Protein 73 (GP73). Studies comparing patients with HCC and cirrhosis with normal controls suggested that GP73 is specific for patients with HCC; however, patients with other liver tumors were not included. We therefore studied the predictive value of GP73 in differentiating between solid benign and malignant liver tumors. MATERIALS AND METHODS: This study included 264 patients: 88 patients with HCC, 88 with hepatocellular adenoma (HCA), and 88 with focal nodal hyperplasia (FNH). A blood sample was collected from each patient to measure GP73 levels using a quantitative ELISA assay and differences in outcome between subgroups were compared. The receiver operating characteristic (ROC) curve, sensitivity and specificity of GP73 were calculated and compared to alpha-fetoprotein (AFP) levels. RESULTS: When comparing malignant and benign liver tumors the area under ROC was 0.701 and 0.912 for GP73 and AFP respectively. Test characteristics revealed a sensitivity of 60% for GP73 and 65% for AFP; in addition the specificity was 77% for GP73 and 96% for AFP. CONCLUSION: Although the literature suggests that GP73 is a valuable serum marker in patients with HCC, the serum concentration may also be increased in patients with solid benign liver tumors. Therefore, a GP73 assay is less suitable for discriminating between primary malignant and benign tumors of the liver. Public Library of Science 2014-07-17 /pmc/articles/PMC4102481/ /pubmed/25033446 http://dx.doi.org/10.1371/journal.pone.0100187 Text en © 2014 Bröker et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bröker, Mirelle E. E. Ijzermans, Jan N. M. Witjes, Caroline D. M. van Vuuren, Hanneke J. de Man, Robert A. The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors |
title | The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors |
title_full | The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors |
title_fullStr | The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors |
title_full_unstemmed | The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors |
title_short | The Predictive Value of Golgi Protein 73 in Differentiating Benign from Malignant Liver Tumors |
title_sort | predictive value of golgi protein 73 in differentiating benign from malignant liver tumors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102481/ https://www.ncbi.nlm.nih.gov/pubmed/25033446 http://dx.doi.org/10.1371/journal.pone.0100187 |
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