Galectin-3 expression is induced in cirrhotic liver and hepatocellular carcinoma

Int J Cancer. 1999 May 17;81(4):519-26. doi: 10.1002/(sici)1097-0215(19990517)81:4<519::aid-ijc3>3.0.co;2-0.

Abstract

Galectins are a family of beta-galactoside-binding animal lectins. In particular, a widely studied member galectin-3, previously designated as epsilonBP, CBP35, Mac-2, L-29 and L-34, has been associated with assorted processes such as cell growth, tumor transformation and metastasis. Galectin-3 is expressed in various tissues and organs but is significantly absent in normal hepatocytes. However, evaluation of patient liver biopsies for galectin-3 expression resulted in the finding that hepatocellular carcinoma (HCC) frequently expressed significant levels of this lectin (76% immunohistochemically positive). Further investigation revealed that galectin-3 expression in HCC is independent of whether the patient had prior hepatitis B virus infection: 14 of 18 HCC cases from HBV- patients, and 5 of 7 cases from HBV patients demonstrated positive galectin-3 immunohistochemistry. However, co-transfection studies using a galectin-3 promoter construct and an HBV-X protein (HBV-X) expression vector demonstrated that galectin-3 expression can occur through transactivation of the lectin promoter by HBV-X. Based on presently known properties of this lectin, it is possible that deregulated expression of galectin-3 can result in tumor transformation and invasiveness, or confer propensity for tumor cell survival. In addition, galectin-3 was abundantly expressed in cirrhotic liver in peripheral distribution within regenerating nodules. Such galectin-3 expression in rapidly proliferating hepatocytes in cirrhotic liver may be a result of the high mitotic index. Alternatively, it is possible that proliferating cells expressing galectin-3 are in the process of being transformed, thus indicating an early neoplastic event.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, Differentiation / analysis
  • Antigens, Differentiation / genetics*
  • Biopsy
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / pathology
  • Galectin 3
  • Gene Expression Regulation
  • Gene Expression Regulation, Neoplastic
  • Hepatitis B / complications
  • Hepatitis B / pathology
  • Hepatitis B Antigens / genetics
  • Hepatitis B Antigens / metabolism
  • Humans
  • Immunohistochemistry
  • Lectins / analysis
  • Lectins / genetics
  • Liver / cytology
  • Liver / metabolism
  • Liver / pathology
  • Liver Cirrhosis / genetics*
  • Liver Cirrhosis / pathology
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / pathology
  • Mice
  • Organ Specificity
  • Promoter Regions, Genetic
  • Spleen / metabolism
  • Thymus Gland / metabolism
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcriptional Activation
  • Tumor Cells, Cultured
  • Viral Regulatory and Accessory Proteins

Substances

  • Antigens, Differentiation
  • Galectin 3
  • Hepatitis B Antigens
  • Lectins
  • Trans-Activators
  • Viral Regulatory and Accessory Proteins
  • hepatitis B virus X protein