Elevation of serum MAGE-4 protein levels and prediction of hepatocellular carcinogenesis in patients with liver cirrhosis

Jpn J Cancer Res. 2002 Apr;93(4):453-8. doi: 10.1111/j.1349-7006.2002.tb01277.x.

Abstract

Early detection of hepatocellular carcinoma (HCC) is clinically important because advanced HCC limits treatment modalities for the cancer. We have previously reported that serum levels of MAGE-4 protein are strongly associated with the development of HCC. The present study was designed to determine whether elevated serum MAGE-4 protein levels can predict hepatocellular carcinogenesis in patients with liver cirrhosis before clinical diagnosis. Among 62 cirrhotic patients, 28 patients were diagnosed with HCC during the follow-up period. The levels of MAGE-4 protein and alpha-fetoprotein (AFP) were significantly elevated in cirrhotic patients with HCC. Univariate and multivariate analyses suggest that elevated serum MAGE-4 protein is more significant than AFP. Importantly, retrospective analysis of prefrozen sera of cirrhotic patients revealed a transient or continuous elevation of serum MAGE-4 protein levels in 14 of 28 cirrhotic patients with HCC (50%) before clinical diagnosis. In contrast, elevated serum MAGE-4 protein levels were observed in 3 of 33 cirrhotic patients without HCC (9%), and in 2 of 34 hepatitic patients (6%). These results indicate that elevated serum MAGE-4 protein levels can be a predictive marker of hepatocellular carcinogenesis in cirrhotic patients, thereby enabling us to treat patients at an earlier stage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antibodies, Monoclonal / chemistry
  • Antigens, Neoplasm
  • Carcinoma, Hepatocellular / blood*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Fibrosis / complications
  • Follow-Up Studies
  • Hepatitis / blood*
  • Humans
  • Kinetics
  • Liver Cirrhosis / blood*
  • Liver Neoplasms / blood*
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Neoplasm Proteins / blood*
  • Odds Ratio
  • Retrospective Studies
  • Time Factors
  • alpha-Fetoproteins / biosynthesis

Substances

  • Antibodies, Monoclonal
  • Antigens, Neoplasm
  • MAGEA4 protein, human
  • Neoplasm Proteins
  • alpha-Fetoproteins