Golgi protein 73, not Glypican-3, may be a tumor marker complementary to α-Fetoprotein for hepatocellular carcinoma diagnosis

Background and Aim This study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican‐3 (GPC‐3) as tumor markers for diagnosis of hepatocellular carcinoma (HCC). Methods A total of 257 subjects were enrolled and consisted of 61 healthy controls, 32 hepatitis B virus carrier...

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Published inJournal of gastroenterology and hepatology Vol. 29; no. 3; pp. 597 - 602
Main Authors Wang, Yichen, Yang, Huayu, Xu, Haifeng, Lu, Xin, Sang, Xinting, Zhong, Shouxian, Huang, Jiefu, Mao, Yilei
Format Journal Article
LanguageEnglish
Published Australia Blackwell Publishing Ltd 01.03.2014
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Abstract Background and Aim This study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican‐3 (GPC‐3) as tumor markers for diagnosis of hepatocellular carcinoma (HCC). Methods A total of 257 subjects were enrolled and consisted of 61 healthy controls, 32 hepatitis B virus carriers, 80 cirrhosis patients, and 84 HCC patients. Diagnosis was performed based on established clinical procedure. Serum GP73, GPC‐3, and α‐fetoprotein were measured. Receiving operating characteristic (ROC) curves were plotted to determine the sensitivity and specificity of each serum marker and their combinations. Result Serum GP73 levels were significantly increased in HCC patients. No significant differences were observed between GP73 and α‐fetoprotein (AFP) as markers for HCC diagnosis. However, GP73 was more sensitive than AFP in the diagnosis of small HCC. A combination of GP73 and AFP tests increased the sensitivity and specificity for HCC diagnosis. The area under the ROC curve (AUC) of combined test was 0.93 compared with 0.88 for GP73 and 0.90 for AFP alone. GPC‐3 tests were negative in all 84 HCC patients. The AUC for GPC‐3 is 0.43, indicating that serum GPC‐3 was not an effective tumor marker for HCC diagnosis. Conclusion Serum GP73 is a potential tumor marker for HCC diagnosis, especially for differential diagnosis of small HCC and cirrhosis. The combination of GP73 and AFP is more sensitive than AFP alone. Serum GPC‐3 does not appear to be an effective tumor marker for HCC diagnosis.
AbstractList This study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican-3 (GPC-3) as tumor markers for diagnosis of hepatocellular carcinoma (HCC). A total of 257 subjects were enrolled and consisted of 61 healthy controls, 32 hepatitis B virus carriers, 80 cirrhosis patients, and 84 HCC patients. Diagnosis was performed based on established clinical procedure. Serum GP73, GPC-3, and α-fetoprotein were measured. Receiving operating characteristic (ROC) curves were plotted to determine the sensitivity and specificity of each serum marker and their combinations. Serum GP73 levels were significantly increased in HCC patients. No significant differences were observed between GP73 and α-fetoprotein (AFP) as markers for HCC diagnosis. However, GP73 was more sensitive than AFP in the diagnosis of small HCC. A combination of GP73 and AFP tests increased the sensitivity and specificity for HCC diagnosis. The area under the ROC curve (AUC) of combined test was 0.93 compared with 0.88 for GP73 and 0.90 for AFP alone. GPC-3 tests were negative in all 84 HCC patients. The AUC for GPC-3 is 0.43, indicating that serum GPC-3 was not an effective tumor marker for HCC diagnosis. Serum GP73 is a potential tumor marker for HCC diagnosis, especially for differential diagnosis of small HCC and cirrhosis. The combination of GP73 and AFP is more sensitive than AFP alone. Serum GPC-3 does not appear to be an effective tumor marker for HCC diagnosis.
Background and Aim This study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican‐3 (GPC‐3) as tumor markers for diagnosis of hepatocellular carcinoma (HCC). Methods A total of 257 subjects were enrolled and consisted of 61 healthy controls, 32 hepatitis B virus carriers, 80 cirrhosis patients, and 84 HCC patients. Diagnosis was performed based on established clinical procedure. Serum GP73, GPC‐3, and α‐fetoprotein were measured. Receiving operating characteristic (ROC) curves were plotted to determine the sensitivity and specificity of each serum marker and their combinations. Result Serum GP73 levels were significantly increased in HCC patients. No significant differences were observed between GP73 and α‐fetoprotein (AFP) as markers for HCC diagnosis. However, GP73 was more sensitive than AFP in the diagnosis of small HCC. A combination of GP73 and AFP tests increased the sensitivity and specificity for HCC diagnosis. The area under the ROC curve (AUC) of combined test was 0.93 compared with 0.88 for GP73 and 0.90 for AFP alone. GPC‐3 tests were negative in all 84 HCC patients. The AUC for GPC‐3 is 0.43, indicating that serum GPC‐3 was not an effective tumor marker for HCC diagnosis. Conclusion Serum GP73 is a potential tumor marker for HCC diagnosis, especially for differential diagnosis of small HCC and cirrhosis. The combination of GP73 and AFP is more sensitive than AFP alone. Serum GPC‐3 does not appear to be an effective tumor marker for HCC diagnosis.
This study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican-3 (GPC-3) as tumor markers for diagnosis of hepatocellular carcinoma (HCC).BACKGROUND AND AIMThis study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican-3 (GPC-3) as tumor markers for diagnosis of hepatocellular carcinoma (HCC).A total of 257 subjects were enrolled and consisted of 61 healthy controls, 32 hepatitis B virus carriers, 80 cirrhosis patients, and 84 HCC patients. Diagnosis was performed based on established clinical procedure. Serum GP73, GPC-3, and α-fetoprotein were measured. Receiving operating characteristic (ROC) curves were plotted to determine the sensitivity and specificity of each serum marker and their combinations.METHODSA total of 257 subjects were enrolled and consisted of 61 healthy controls, 32 hepatitis B virus carriers, 80 cirrhosis patients, and 84 HCC patients. Diagnosis was performed based on established clinical procedure. Serum GP73, GPC-3, and α-fetoprotein were measured. Receiving operating characteristic (ROC) curves were plotted to determine the sensitivity and specificity of each serum marker and their combinations.Serum GP73 levels were significantly increased in HCC patients. No significant differences were observed between GP73 and α-fetoprotein (AFP) as markers for HCC diagnosis. However, GP73 was more sensitive than AFP in the diagnosis of small HCC. A combination of GP73 and AFP tests increased the sensitivity and specificity for HCC diagnosis. The area under the ROC curve (AUC) of combined test was 0.93 compared with 0.88 for GP73 and 0.90 for AFP alone. GPC-3 tests were negative in all 84 HCC patients. The AUC for GPC-3 is 0.43, indicating that serum GPC-3 was not an effective tumor marker for HCC diagnosis.RESULTSerum GP73 levels were significantly increased in HCC patients. No significant differences were observed between GP73 and α-fetoprotein (AFP) as markers for HCC diagnosis. However, GP73 was more sensitive than AFP in the diagnosis of small HCC. A combination of GP73 and AFP tests increased the sensitivity and specificity for HCC diagnosis. The area under the ROC curve (AUC) of combined test was 0.93 compared with 0.88 for GP73 and 0.90 for AFP alone. GPC-3 tests were negative in all 84 HCC patients. The AUC for GPC-3 is 0.43, indicating that serum GPC-3 was not an effective tumor marker for HCC diagnosis.Serum GP73 is a potential tumor marker for HCC diagnosis, especially for differential diagnosis of small HCC and cirrhosis. The combination of GP73 and AFP is more sensitive than AFP alone. Serum GPC-3 does not appear to be an effective tumor marker for HCC diagnosis.CONCLUSIONSerum GP73 is a potential tumor marker for HCC diagnosis, especially for differential diagnosis of small HCC and cirrhosis. The combination of GP73 and AFP is more sensitive than AFP alone. Serum GPC-3 does not appear to be an effective tumor marker for HCC diagnosis.
Author Xu, Haifeng
Huang, Jiefu
Zhong, Shouxian
Yang, Huayu
Sang, Xinting
Wang, Yichen
Lu, Xin
Mao, Yilei
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Keywords glypican-3
differential diagnosis
α-fetoprotein
Golgi protein 73
hepatocellular carcinoma
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References_xml – reference: Filmus J, Shi W, Wong ZM, Wong MJ. Identification of a new membrane-bound heparan sulphate proteoglycan. Biochem. J. 1995; 311: 561-565.
– reference: Marrero JA, Feng Z, Wang Y et al. Alpha-fetoprotein, des-gamma carboxyprothrombin, and lectin-bound alpha-fetoprotein in early hepatocellular carcinoma. Gastroenterology 2009; 137: 110-118.
– reference: Mao Y, Yang H, Xu H et al. Golgi protein 73 (GOLPH2) is a valuable serum marker for hepatocellular carcinoma. Gut 2010; 59: 1687-1693.
– reference: Witjes CD, van Aalten SM, Steyerberg EW et al. Recently introduced biomarkers for screening of hepatocellular carcinoma: a systematic review and meta-analysis. Hepatol. Int. 2013; 7: 59-64.
– reference: Pilia G, Hughes-Benzie RM, MacKenzie A et al. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nat. Genet. 1996; 12: 241-247.
– reference: Ozkan H, Erdal H, Kocak E et al. Diagnostic and prognostic role of serum glypican 3 in patients with hepatocellular carcinoma. J. Clin. Lab. Anal. 2011; 25: 350-353.
– reference: Maitra A, Thuluvath PJ. GP73 and liver disease: a (Golgi) complex enigma. Am. J. Gastroenterol. 2004; 99: 1096-1098.
– reference: Yano Y, Seo Y, Azuma T, Hayashi Y. Hepatitis B virus and host factors. Hepatobiliary Surg. Nutr. 2013; 2: 121-123.
– reference: Capurro M, Wanless IR, Sherman M et al. Glypican-3: a novel serum and histochemical marker for hepatocellular carcinoma. Gastroenterology 2003; 125: 89-97.
– reference: Marrero JA, Romano PR, Nikolaeva O et al. GP73, a resident Golgi glycoprotein, is a novel serum marker for hepatocellular carcinoma. J. Hepatol. 2005; 43: 1007-1012.
– reference: Chen M, Li G, Yan J et al. Reevaluation of glypican-3 as a serological marker for hepatocellular carcinoma. Clin. Chim. Acta 2013; 423: 105-111.
– reference: Block TM, Comunale MA, Lowman M et al. Use of targeted glycoproteomics to identify serum glycoproteins that correlate with liver cancer in woodchucks and humans. Proc. Natl Acad. Sci. U.S.A. 2005; 102: 779-784.
– reference: Murthy SS, Shen T, De Rienzo A et al. Expression of GPC3, an X-linked recessive overgrowth gene, is silenced in malignant mesothelioma. Oncogene 2000; 19: 410-416.
– reference: Gonzalez AD, Kaya M, Shi W et al. OCI-5/GPC3, a glypican encoded by a gene that is mutated in the Simpson-Golabi-Behmel overgrowth syndrome, induces apoptosis in a cell line-specific manner. J. Cell Biol. 1998; 141: 1407-1414.
– reference: Trevisani F, D'Intino PE, Morselli-Labate AM et al. Serum alpha-fetoprotein for diagnosis of hepatocellular carcinoma in patients with chronic liver disease: influence of HBsAg and anti-HCV status. J. Hepatol. 2001; 34: 570-575.
– reference: Kladney RD, Tollefson AE, Wold WS, Fimmel CJ. Upregulation of the Golgi protein GP73 by adenovirus infection requires the E1A CtBP interaction domain. Virology 2002; 301: 236-246.
– reference: Saunders S, Paine-Saunders S, Lander AD. Expression of the cell surface proteoglycan glypican-5 is developmentally regulated in kidney, limb, and brain. Dev. Biol. 1997; 190: 78-93.
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Snippet Background and Aim This study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican‐3 (GPC‐3) as tumor markers for diagnosis of...
This study aimed to evaluate the effectiveness of serum Golgi protein 73 (GP73) and Glypican-3 (GPC-3) as tumor markers for diagnosis of hepatocellular...
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pubmed
wiley
istex
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StartPage 597
SubjectTerms Adult
Aged
alpha-Fetoproteins - analysis
Biomarkers, Tumor - blood
Carcinoma, Hepatocellular - diagnosis
Carcinoma, Hepatocellular - pathology
Diagnosis, Differential
differential diagnosis
Female
glypican-3
Glypicans - blood
Golgi protein 73
hepatocellular carcinoma
Humans
Liver Neoplasms - diagnosis
Liver Neoplasms - pathology
Male
Membrane Proteins - blood
Middle Aged
ROC Curve
Sensitivity and Specificity
α-fetoprotein
Title Golgi protein 73, not Glypican-3, may be a tumor marker complementary to α-Fetoprotein for hepatocellular carcinoma diagnosis
URI https://api.istex.fr/ark:/67375/WNG-ZF7B7NBK-K/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjgh.12461
https://www.ncbi.nlm.nih.gov/pubmed/24236824
https://www.proquest.com/docview/1503542797
Volume 29
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