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Diagnostic value of angiopoietin-like protein 2 for CHB-related hepatocellular carcinoma

Authors Zhou J, Yang W, Zhang S, He X, Lin J, Zhou T, Li Y, Wang G, Chen J

Received 27 May 2019

Accepted for publication 15 July 2019

Published 29 July 2019 Volume 2019:11 Pages 7159—7169

DOI https://doi.org/10.2147/CMAR.S217170

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Colin Mak

Peer reviewer comments 3

Editor who approved publication: Dr Eileen O'Reilly


Jiyuan Zhou,1 Wanna Yang,2 Shu Zhang,1 Xuanqiu He,3 Jiatian Lin,1 Tao Zhou,1 Yaqin Li,3 Guiqiang Wang,2,4 Junhui Chen1

1Intervention and Cell Therapy Center, Peking University Shenzhen Hospital, Shenzhen Peking University-the Hong Kong University of Science and Technology Medical Center, Shenzhen 518035, Guangdong, People’s Republic of China; 2Department of Infectious Disease, Center for Liver Disease, Peking University First Hospital, Beijing 100034, People’s Republic of China; 3Department of Infectious Disease, Peking University Shenzhen Hospital, Shenzhen 518035, Guangdong, People’s Republic of China; 4The Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang University, Hangzhou 310013, Zhejiang, People’s Republic of China

Purpose: Angiopoietin-like protein 2 (ANGPTL2) is a secretory glycoprotein with various functions in vascular biology, inflammation and tumor development. As shown in our previous studies, ANGPTL2 expression positively correlates with liver fibrosis stages in chronic hepatitis B (CHB) patients. The aim of this study was further to assess whether ANGPTL2 represents a potential biomarker for detecting hepatocellular carcinoma (HCC).
Patients and methods: This study enrolled 361 participants including healthy controls (HCs) and patients with CHB, liver cirrhosis (LC) and HCC. A discovery cohort consisted of 35 HCs and 55 patients with HCC. A total of 271 participants, including 45 HCs, 125 patients with CHB, 38 patients with LC, and 63 patients with HCC were enrolled in a validation cohort. Serum ANGPTL2 levels were detected using a human ANGPTL2 assay kit, and hepatic expression of ANGPTL2 was analyzed using immunohistochemistry.
Results: In the discovery cohort, a significantly higher serum ANGPTL2 level was detected in HCC than in HCs (73.49±33.87 vs 30.54±9.86; p<0.001). The results of the receiver operating characteristic curve indicated a significantly higher area under the curve for the ability of the ANGPTL2 to predict HCC than alpha fetoprotein (AFP). In the validation cohort, serum ANGPTL2 level gradually increased with the progression of chronic hepatitis B virus infection and reached the highest level in HCC. Immunohistochemical staining also confirmed these findings. The serum ANGPTL2 displayed better diagnostic efficiency not only for differentiating HCC from HC but also for differentiating HCC from high-risk controls (CHB+LC). Furthermore, the combination of ANGPTL2 and AFP may increase the diagnostic accuracy for HCC compared to ANGPTL2 or AFP alone. Importantly, ANGPTL2 levels also correlated with the detection of AFP-negative HCC.
Conclusions: ANGPTL2 may be used as a promising biomarker for the diagnosis of CHB-related HCC.

Keywords: ANGPTL2, CHB, HCC, diagnosis


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