Analyses of autoantibodies against tumor-associated antigens in patients with hepatocellular carcinoma

Int J Oncol. 2005 Oct;27(4):1079-85.

Abstract

Autoantibodies against tumor-associated antigens (TAAs) such as insulin-like growth factor II mRNA-binding proteins (IMPs), p53, c-myc, and survivin were analyzed in patients with hepatocellular carcinoma (HCC), using recombinant proteins of these antigens. Eight of 86 (9.3%) HCC patients had one or more of these autoantibodies. However, serum alpha-fetoprotein (AFP) levels ranged within normal limits in HCC patients with anti-TAAs except for one case with anti-IMP1. One of the HCC patients had autoantibodies against IMP1, IMP3 and p53 before the diagnosis of HCC. These findings may indicate that anti-TAAs seem to be supplementary serological markers for the diagnosis of HCC in AFP-negative cases and that autoantibodies against IMP1, IMP3 and p53 are candidates for predictive markers of HCC development.

MeSH terms

  • Antigens, Neoplasm / chemistry*
  • Autoantibodies / chemistry*
  • Biomarkers, Tumor / metabolism
  • Blotting, Western
  • Carcinoma, Hepatocellular / diagnosis
  • Carcinoma, Hepatocellular / metabolism*
  • DNA, Complementary / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Fibrosis
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Liver / metabolism
  • Liver Neoplasms / diagnosis
  • Liver Neoplasms / metabolism*
  • Microtubule-Associated Proteins / metabolism
  • Neoplasm Proteins / metabolism
  • Proto-Oncogene Proteins c-myc / metabolism
  • RNA, Messenger / metabolism
  • Recombinant Proteins / chemistry
  • Survivin
  • Tumor Suppressor Protein p53 / metabolism
  • alpha-Fetoproteins / biosynthesis

Substances

  • Antigens, Neoplasm
  • Autoantibodies
  • BIRC5 protein, human
  • Biomarkers, Tumor
  • DNA, Complementary
  • Inhibitor of Apoptosis Proteins
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • Recombinant Proteins
  • Survivin
  • Tumor Suppressor Protein p53
  • alpha-Fetoproteins