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Glypican 3 as a Serum Marker for Hepatoblastoma
Hepatoblastoma (HB) is the most common primary liver cancer in children. The conventional serum marker for HB, alpha-fetoprotein (AFP), has its limitations. Novel serum markers need to be explored. Glypican 3 (GPC3) has been reported to be an excellent histological immunomarker for HB. However, the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381115/ https://www.ncbi.nlm.nih.gov/pubmed/28378832 http://dx.doi.org/10.1038/srep45932 |
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author | Zhou, Shengmei O’Gorman, Maurice R. G. Yang, Fusheng Andresen, Kevin Wang, Larry |
author_facet | Zhou, Shengmei O’Gorman, Maurice R. G. Yang, Fusheng Andresen, Kevin Wang, Larry |
author_sort | Zhou, Shengmei |
collection | PubMed |
description | Hepatoblastoma (HB) is the most common primary liver cancer in children. The conventional serum marker for HB, alpha-fetoprotein (AFP), has its limitations. Novel serum markers need to be explored. Glypican 3 (GPC3) has been reported to be an excellent histological immunomarker for HB. However, the clinical value of serum GPC3 in patients with HB is unknown. A total of 184 serum samples were tested for both GPC3 by ELISA, and AFP by immunometric assay. Of these, 134 were from 32 patients with HB at three treatment stages, 30 from age-matched patients with benign hepatobiliary disorders (BHD) and 20 from age-matched “normal controls”(NC). We found that the GPC3 levels in HB pretreatment group were significantly higher than those in NC group and HB remission group but not statistically different from those in BHD group and HB during treatment group. In contrast, AFP showed significant differences among different groups. The areas under the receiver operating curve (AUROC) value, sensitivity and specificity of GPC3 for HB pretreatment group versus all controls were all significantly lower than those of AFP. Serum GPC3 levels were not associated with prognostic parameters. We concluded that GPC3 is inferior to AFP as a serum marker for HB. |
format | Online Article Text |
id | pubmed-5381115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53811152017-04-10 Glypican 3 as a Serum Marker for Hepatoblastoma Zhou, Shengmei O’Gorman, Maurice R. G. Yang, Fusheng Andresen, Kevin Wang, Larry Sci Rep Article Hepatoblastoma (HB) is the most common primary liver cancer in children. The conventional serum marker for HB, alpha-fetoprotein (AFP), has its limitations. Novel serum markers need to be explored. Glypican 3 (GPC3) has been reported to be an excellent histological immunomarker for HB. However, the clinical value of serum GPC3 in patients with HB is unknown. A total of 184 serum samples were tested for both GPC3 by ELISA, and AFP by immunometric assay. Of these, 134 were from 32 patients with HB at three treatment stages, 30 from age-matched patients with benign hepatobiliary disorders (BHD) and 20 from age-matched “normal controls”(NC). We found that the GPC3 levels in HB pretreatment group were significantly higher than those in NC group and HB remission group but not statistically different from those in BHD group and HB during treatment group. In contrast, AFP showed significant differences among different groups. The areas under the receiver operating curve (AUROC) value, sensitivity and specificity of GPC3 for HB pretreatment group versus all controls were all significantly lower than those of AFP. Serum GPC3 levels were not associated with prognostic parameters. We concluded that GPC3 is inferior to AFP as a serum marker for HB. Nature Publishing Group 2017-04-05 /pmc/articles/PMC5381115/ /pubmed/28378832 http://dx.doi.org/10.1038/srep45932 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhou, Shengmei O’Gorman, Maurice R. G. Yang, Fusheng Andresen, Kevin Wang, Larry Glypican 3 as a Serum Marker for Hepatoblastoma |
title | Glypican 3 as a Serum Marker for Hepatoblastoma |
title_full | Glypican 3 as a Serum Marker for Hepatoblastoma |
title_fullStr | Glypican 3 as a Serum Marker for Hepatoblastoma |
title_full_unstemmed | Glypican 3 as a Serum Marker for Hepatoblastoma |
title_short | Glypican 3 as a Serum Marker for Hepatoblastoma |
title_sort | glypican 3 as a serum marker for hepatoblastoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381115/ https://www.ncbi.nlm.nih.gov/pubmed/28378832 http://dx.doi.org/10.1038/srep45932 |
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