Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Shengmei, O’Gorman, Maurice R. G., Yang, Fusheng, Andresen, Kevin, Wang, Larry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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
_version_ 1782519874886565888
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
work_keys_str_mv AT zhoushengmei glypican3asaserummarkerforhepatoblastoma
AT ogormanmauricerg glypican3asaserummarkerforhepatoblastoma
AT yangfusheng glypican3asaserummarkerforhepatoblastoma
AT andresenkevin glypican3asaserummarkerforhepatoblastoma
AT wanglarry glypican3asaserummarkerforhepatoblastoma