Cargando…

Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is a type of cancer with a very poor prognosis. Although α-fetoprotein (AFP) is the most effective marker available to detect HCC, the sensitivity and specificity are not optimal. Therefore, there is a need for the development of more sensitive and specific methods tha...

Descripción completa

Detalles Bibliográficos
Autores principales: SHAO, QING, REN, PENGFEI, LI, YANG, PENG, BO, DAI, LIPING, LEI, NINGJING, YAO, WU, ZHAO, GANG, LI, LINGGEN, ZHANG, JIANYING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582881/
https://www.ncbi.nlm.nih.gov/pubmed/22692946
http://dx.doi.org/10.3892/ijo.2012.1515
_version_ 1782260623273361408
author SHAO, QING
REN, PENGFEI
LI, YANG
PENG, BO
DAI, LIPING
LEI, NINGJING
YAO, WU
ZHAO, GANG
LI, LINGGEN
ZHANG, JIANYING
author_facet SHAO, QING
REN, PENGFEI
LI, YANG
PENG, BO
DAI, LIPING
LEI, NINGJING
YAO, WU
ZHAO, GANG
LI, LINGGEN
ZHANG, JIANYING
author_sort SHAO, QING
collection PubMed
description Hepatocellular carcinoma (HCC) is a type of cancer with a very poor prognosis. Although α-fetoprotein (AFP) is the most effective marker available to detect HCC, the sensitivity and specificity are not optimal. Therefore, there is a need for the development of more sensitive and specific methods that can supplement AFP in the early detection of this cancer. In this study, autoantibody responses to glucose-regulated protein 78 (GRP78) were evaluated by enzyme-linked immunosorbent assay (ELISA), western blotting and indirect immunofluorescence assay in sera from patients with HCC, liver cirrhosis (LC) and chronic hepatitis (CH), as well as from normal human individuals. Immunohistochemistry (IHC) with tissue array slides was also preformed to analyze protein expression profiles of GRP78 in HCC and control tissues. The prevalence of autoantibodies against GRP78 was 35.5% (27/76) in HCC, which was significantly higher than that in LC, CH and normal human sera (NHS; P<0.01). The average titer of autoantibodies against GRP78 in HCC sera was higher compared to that in LC, CH and NHS(P<0.01). When both autoantibodies against GRP78 and AFP were used simultaneously as diagnostic markers, sensitivity reached 71.4%. Our data indicate that anti-GRP78 autoantibodies may be potential diagnostic markers for HCC, especially in conjunction with AFP.
format Online
Article
Text
id pubmed-3582881
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-35828812013-03-04 Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma SHAO, QING REN, PENGFEI LI, YANG PENG, BO DAI, LIPING LEI, NINGJING YAO, WU ZHAO, GANG LI, LINGGEN ZHANG, JIANYING Int J Oncol Articles Hepatocellular carcinoma (HCC) is a type of cancer with a very poor prognosis. Although α-fetoprotein (AFP) is the most effective marker available to detect HCC, the sensitivity and specificity are not optimal. Therefore, there is a need for the development of more sensitive and specific methods that can supplement AFP in the early detection of this cancer. In this study, autoantibody responses to glucose-regulated protein 78 (GRP78) were evaluated by enzyme-linked immunosorbent assay (ELISA), western blotting and indirect immunofluorescence assay in sera from patients with HCC, liver cirrhosis (LC) and chronic hepatitis (CH), as well as from normal human individuals. Immunohistochemistry (IHC) with tissue array slides was also preformed to analyze protein expression profiles of GRP78 in HCC and control tissues. The prevalence of autoantibodies against GRP78 was 35.5% (27/76) in HCC, which was significantly higher than that in LC, CH and normal human sera (NHS; P<0.01). The average titer of autoantibodies against GRP78 in HCC sera was higher compared to that in LC, CH and NHS(P<0.01). When both autoantibodies against GRP78 and AFP were used simultaneously as diagnostic markers, sensitivity reached 71.4%. Our data indicate that anti-GRP78 autoantibodies may be potential diagnostic markers for HCC, especially in conjunction with AFP. D.A. Spandidos 2012-06-12 /pmc/articles/PMC3582881/ /pubmed/22692946 http://dx.doi.org/10.3892/ijo.2012.1515 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
SHAO, QING
REN, PENGFEI
LI, YANG
PENG, BO
DAI, LIPING
LEI, NINGJING
YAO, WU
ZHAO, GANG
LI, LINGGEN
ZHANG, JIANYING
Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma
title Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma
title_full Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma
title_fullStr Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma
title_full_unstemmed Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma
title_short Autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma
title_sort autoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582881/
https://www.ncbi.nlm.nih.gov/pubmed/22692946
http://dx.doi.org/10.3892/ijo.2012.1515
work_keys_str_mv AT shaoqing autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT renpengfei autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT liyang autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT pengbo autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT dailiping autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT leiningjing autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT yaowu autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT zhaogang autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT lilinggen autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma
AT zhangjianying autoantibodiesagainstglucoseregulatedprotein78asserologicaldiagnosticbiomarkersinhepatocellularcarcinoma