Abstract
Hepatocellular carcinoma (HCC) patients commonly experience poor overall survival (OS) and disease-free survival (DFS) after curative surgical resection. Glypican-3 (GPC3) has been suggested as a prognostic biomarker for post-operative survival. However, few to none of these studies have included South Korean patients. This study aimed to determine GPC3 expression rate, clinical correlation, and post-operative prognostic value in South Korean HCC patients who underwent curative surgical resection. Surgically resected tissues from 185 HCC patients were collected and assembled into tissue microarrays (TMAs), which were stained for GPC3 by immunohistochemistry. GPC3 expression rates were correlated with clinicopathological information, and survival analyses were performed to assess the prognostic value of GPC3. GPC3 expression was present in 153 patients (82.7%). GPC3-positive patients were younger with higher frequencies of microvascular invasion and higher AFP levels than GPC3-negative patients. There was no significant difference in survival between GPC3-negative and GPC3-positive patients. Based on multivariate analysis, GPC3 expression was not a prognostic marker for post-operative survival. In South Korean HCC patients, GPC3 expression was more frequent in HCCs with aggressive features, but it was not an independent prognostic biomarker.
Keywords
biomarkers
glypican-3
hepatocellular carcinoma
immunohistochemistry
prognosis
MeSH Terms
Adult
Aged
Aged, 80 and over
Biomarkers, Tumor/genetics
Body Mass Index
Carcinoma, Hepatocellular/diagnosis,genetics,surgery
Female
Gene Expression Regulation, Neoplastic
Glypicans/genetics,metabolism
Humans
Immunohistochemistry
Liver Neoplasms/diagnosis,genetics,surgery
Male
Middle Aged
Multivariate Analysis
Postoperative Complications/genetics
Prognosis
Proportional Hazards Models
Republic of Korea
Retrospective Studies
Survival Analysis
Transcriptome
Chemicals
Biomarkers, Tumor
GPC3 protein, human
Glypicans
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Jeon Yejoo
Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Kim Haeryoung
Department of Pathology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Jang Eun Sun
Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Hong Sukho
Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Kim Jin Wook
Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Yoon Yoo-Seok
Department of Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Cho Jai Young
Department of Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Han Ho-Seong
Department of Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Jeong Sook-Hyang
Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.