Cargando…
Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients
The aim of this study was to explore the value of autoantibody to GNAS in the early detection of hepatocellular carcinoma (HCC). In a large-scale sample set of 912 participants (228 cases in each of HCC, liver cirrhosis (LC), chronic hepatitis B (CHB), and normal controls (NCs) groups), autoantibody...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773227/ https://www.ncbi.nlm.nih.gov/pubmed/35052777 http://dx.doi.org/10.3390/biomedicines10010097 |
_version_ | 1784636031189909504 |
---|---|
author | Wang, Xiao Wang, Keyan Qiu, Cuipeng Wang, Bofei Zhang, Xiaojun Ma, Yangcheng Dai, Liping Zhang, Jian-Ying |
author_facet | Wang, Xiao Wang, Keyan Qiu, Cuipeng Wang, Bofei Zhang, Xiaojun Ma, Yangcheng Dai, Liping Zhang, Jian-Ying |
author_sort | Wang, Xiao |
collection | PubMed |
description | The aim of this study was to explore the value of autoantibody to GNAS in the early detection of hepatocellular carcinoma (HCC). In a large-scale sample set of 912 participants (228 cases in each of HCC, liver cirrhosis (LC), chronic hepatitis B (CHB), and normal controls (NCs) groups), autoantibody to GNAS was detected with a positive result in 47.8% of HCC patients, which was significantly higher than that in patients with LC (35.1%), CHB (19.7%), and NCs (19.7%). Further analysis showed that the frequency of autoantibody to GNAS started increasing in compensated cirrhosis patients (37.0%) with a jump in decompensated cirrhosis patients (53.2%) and reached a peak in early HCC patients (62.4%). The increasing autoantibody response to GNAS in patients at different stages was closely associated with the progression of chronic liver lesions. The result from 44 human serial sera demonstrated that 5 of 11 (45.5%) HCC patients had elevated autoantibody to GNAS before and/or at diagnosis of HCC. Moreover, 46.1% and 62.4% of high positive rates in alpha-fetoprotein (AFP) negative and early-stage HCC patients can supplement AFP in early detection of HCC. These findings suggest that autoantibody to GNAS could be used as a potential biomarker for the early detection of HCC. |
format | Online Article Text |
id | pubmed-8773227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87732272022-01-21 Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients Wang, Xiao Wang, Keyan Qiu, Cuipeng Wang, Bofei Zhang, Xiaojun Ma, Yangcheng Dai, Liping Zhang, Jian-Ying Biomedicines Article The aim of this study was to explore the value of autoantibody to GNAS in the early detection of hepatocellular carcinoma (HCC). In a large-scale sample set of 912 participants (228 cases in each of HCC, liver cirrhosis (LC), chronic hepatitis B (CHB), and normal controls (NCs) groups), autoantibody to GNAS was detected with a positive result in 47.8% of HCC patients, which was significantly higher than that in patients with LC (35.1%), CHB (19.7%), and NCs (19.7%). Further analysis showed that the frequency of autoantibody to GNAS started increasing in compensated cirrhosis patients (37.0%) with a jump in decompensated cirrhosis patients (53.2%) and reached a peak in early HCC patients (62.4%). The increasing autoantibody response to GNAS in patients at different stages was closely associated with the progression of chronic liver lesions. The result from 44 human serial sera demonstrated that 5 of 11 (45.5%) HCC patients had elevated autoantibody to GNAS before and/or at diagnosis of HCC. Moreover, 46.1% and 62.4% of high positive rates in alpha-fetoprotein (AFP) negative and early-stage HCC patients can supplement AFP in early detection of HCC. These findings suggest that autoantibody to GNAS could be used as a potential biomarker for the early detection of HCC. MDPI 2022-01-04 /pmc/articles/PMC8773227/ /pubmed/35052777 http://dx.doi.org/10.3390/biomedicines10010097 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Xiao Wang, Keyan Qiu, Cuipeng Wang, Bofei Zhang, Xiaojun Ma, Yangcheng Dai, Liping Zhang, Jian-Ying Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients |
title | Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients |
title_full | Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients |
title_fullStr | Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients |
title_full_unstemmed | Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients |
title_short | Autoantibody to GNAS in Early Detection of Hepatocellular Carcinoma: A Large-Scale Sample Study Combined with Verification in Serial Sera from HCC Patients |
title_sort | autoantibody to gnas in early detection of hepatocellular carcinoma: a large-scale sample study combined with verification in serial sera from hcc patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773227/ https://www.ncbi.nlm.nih.gov/pubmed/35052777 http://dx.doi.org/10.3390/biomedicines10010097 |
work_keys_str_mv | AT wangxiao autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients AT wangkeyan autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients AT qiucuipeng autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients AT wangbofei autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients AT zhangxiaojun autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients AT mayangcheng autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients AT dailiping autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients AT zhangjianying autoantibodytognasinearlydetectionofhepatocellularcarcinomaalargescalesamplestudycombinedwithverificationinserialserafromhccpatients |