Liver Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 15, 2003; 9(4): 710-713
Published online Apr 15, 2003. doi: 10.3748/wjg.v9.i4.710
Glycylproline dipeptidyl aminopeptidase isoenzyme in diagnosis of primary hepatocellular carcinoma
Run-Zhou Ni, Jie-Fei Huang, Ming-Bing Xiao, Mei Li, Xian-Yong Meng
Run-Zhou Ni, Jie-Fei Huang, Ming-Bing Xiao, Mei Li, Xian-Yong Meng, Department of Gastroenterology, Affiliated Hospital of Nantong Medical College, Nantong 226001, Jiangsu Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Run-Zhou Ni, Department of Gastroenterology, Affiliated Hospital of Nantong Medical College, Nantong 226001, Jiangsu Province, China. nirz@public.nt.js.cn
Telephone: +86-513-5119461
Received: September 14, 2002
Revised: October 10, 2002
Accepted: October 17, 2002
Published online: April 15, 2003
Abstract

AIM: To investigate the role of glycylproline dipeptidyl aminopeptidase (GPDA) isoenzyme in the diagnosis of primary hepatocellular carcinoma (PHC), especially in patients with negative alpha-fetoprotein (AFP).

METHODS: A stage gradient polyacrylamide gel discontinuous electrophoresis system was developed to separate serum GPDA isoenzymes, which were determined in 102 patients with PHC, 45 cases with liver cirrhosis, 24 cases with chronic hepatitis, 35 cases with benign liver space-occupying lesions, 20 cases with metastatic liver cancer and 50 cases with extra-hepatic cancer, as well as 80 healthy subjects. The relationships between GPDA isoenzymes and AFP, the sizes of tumors, as well as alanine aminotransferase (ALT) were also analyzed.

RESULTS: Serum GPDA was separated into two isoenzymes, GPDA-S and GPDA-F. The former was positive in all subjects, while the latter was found mainly in majority of PHC (85.3%) and a few cases with liver cirrhosis (11.1%), chronic hepatitis (33.3%), metastatic liver cancer (15.0%) and non-hepatic cancer (16.0%). GPDA-F was negative in all healthy subjects and patients with benign liver space-occupying lesions, including abscess, cysts and angioma. There was no correlation between GPDA-F and AFP concentration or tumor size. GPDA-F was consistently positive and not correlated with ALT in PHC, but GPDA-F often converted to negative as decline of ALT in benign liver diseases. The electrophoretic migration of GPDA-F became sluggish after the treatment of neuraminidase.

CONCLUSION: GPDA-F is a new useful serum marker for PHC. Measurement of serum GPDA-F is helpful in diagnosis of PHC, especially in patients with negative AFP. GPDA-F is one kind of glycoproteins rich in sialic acid.

Keywords: $[Keywords]