Down-regulation in human cancers of DRHC, a novel helicase-like gene from 17q25.1 that inhibits cell growth

Cancer Lett. 2003 Apr 10;193(1):41-7. doi: 10.1016/s0304383502006882.

Abstract

Frequent observations of allelic loss in chromosomal band 17q25.1 in a variety of human cancers have suggested that one or more tumor suppressor genes are normally present in this region. Moreover, a locus responsible for hereditary focal non-epidermolytic palmoplantar keratoderma (tylosis oesophageal cancer; TOC), a condition associated with esophageal cancer, has been mapped to the same band. During efforts to sequence, by shot-gun methods, a 1 Mb target region that we had defined as the DNA segment harboring the putative tumor suppressor gene(s) involved in these events, we identified a novel cDNA, DRHC (down-regulated in human cancers), that showed reduced expression in 28 of 95 (29%) cell lines derived from a variety of human cancers. The full-length cDNA, 6275 bp long, was expressed predominantly in thymus and brain. The predicted 1942-amino-acid product exhibited significant sequence homology to yeast enzymes belonging to the DEAD-helicase superfamily, and appeared to be a Uvr/Rep helicase with a DEXDc consensus domain. Transfection of a DRHC expression vector inhibited growth of cancer cells in liquid medium or soft agar. The results suggest that loss of expression of DRHC may play a role in human carcinogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Northern
  • Brain / metabolism
  • Cell Division
  • Chromosomes, Human, Pair 17*
  • Cloning, Molecular
  • DNA / metabolism
  • DNA Helicases / biosynthesis*
  • DNA Helicases / genetics
  • DNA Helicases / metabolism
  • DNA, Complementary / metabolism
  • Databases as Topic
  • Down-Regulation*
  • Esophageal Neoplasms / genetics
  • Esophageal Neoplasms / metabolism
  • Genes, Tumor Suppressor
  • Genetic Vectors
  • Humans
  • Models, Genetic
  • Neoplasm Proteins
  • Neoplasms / genetics*
  • Neoplasms / metabolism*
  • Polymorphism, Single-Stranded Conformational
  • Protein Structure, Tertiary
  • RNA Helicases
  • Reverse Transcriptase Polymerase Chain Reaction
  • Thymus Gland / metabolism
  • Time Factors
  • Transfection
  • Tumor Cells, Cultured

Substances

  • DNA, Complementary
  • Neoplasm Proteins
  • DNA
  • DNA Helicases
  • MAPK4 protein, human
  • RNA Helicases