Gene signatures in hepatocellular carcinoma (HCC)

Semin Cancer Biol. 2011 Feb;21(1):4-9. doi: 10.1016/j.semcancer.2010.09.002. Epub 2010 Sep 17.

Abstract

Primary hepatocellular carcinoma (HCC) is a significant human cancer globally, with poor prognosis. New and efficacious therapy strategies are needed as well as new biomarkers for early detection of at-risk patients. In this review, we discuss select microarray studies of human HCCs, and propose a gene signature that has promise for clinical/translational application. This gene signature combines the proliferation cluster of genes and the hepatic cancer initiating/stem cell gene cluster for identification of HCCs with poor prognosis. Evidence from cell-based assays identifies the existence of a mechanistic link between these two gene clusters, involving the proliferation cluster gene polo-like kinase 1 (PLK1). We propose that PLK1 is a promising therapy target for HCC.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism
  • Carcinoma, Hepatocellular / genetics*
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Epithelial Cell Adhesion Molecule
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Liver Neoplasms / genetics*
  • Multigene Family
  • Neoplastic Stem Cells / metabolism
  • Polo-Like Kinase 1
  • Polycomb-Group Proteins
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Repressor Proteins / metabolism
  • Signal Transduction

Substances

  • Antigens, Neoplasm
  • Cell Adhesion Molecules
  • Cell Cycle Proteins
  • Epithelial Cell Adhesion Molecule
  • Polycomb-Group Proteins
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • Protein Serine-Threonine Kinases