Cloning, characterization, and chromosomal localization of a gene frequently deleted in human liver cancer (DLC-1) homologous to rat RhoGAP

Cancer Res. 1998 May 15;58(10):2196-9.

Abstract

The isolation of genes involved in cancer development is critical for uncovering the molecular basis of cancer. We report here the isolation of the full-length cDNA and chromosomal localization of a new gene frequently deleted in liver cancer (DLC-1) that was identified by representational difference analysis. Loss of heterozygosity was detected for DLC-1 in 7 of 16 primary hepatocellular carcinomas (HCCs) and in 10 of 11 HCC cell lines. Although mRNA for DLC-1 was expressed in all normal human tissues, it was not expressed in 4 of 14 HCC cell lines. Full-length cDNA for DLC-1 of 3800 bp encodes a protein of 1091 amino acids, has 86% homology with rat p122 RhoGAP gene, and was localized by fluorescence in situ hybridization on chromosome 8 at bands p21.3-22. Deletions on the short arm of chromosome 8 are recurrent in liver, breast, lung, and prostate cancers, suggesting the presence of tumor suppressor genes. DLC-1 may be a tumor suppressor gene in liver cancer as well as in other cancers.

MeSH terms

  • Animals
  • Carcinoma, Hepatocellular / genetics*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 8 / genetics*
  • GTPase-Activating Proteins
  • Gene Deletion
  • Genes, Tumor Suppressor / genetics*
  • Humans
  • Liver Neoplasms / genetics*
  • Loss of Heterozygosity
  • Molecular Sequence Data
  • Proteins / genetics*
  • Rats
  • Tumor Cells, Cultured
  • Tumor Suppressor Proteins*

Substances

  • DLC1 protein, human
  • GTPase-Activating Proteins
  • Proteins
  • Tumor Suppressor Proteins

Associated data

  • GENBANK/AF035119