Patched 2, located in 1p32-34, is not mutated in high stage neuroblastoma tumors

Int J Oncol. 2000 May;16(5):943-9. doi: 10.3892/ijo.16.5.943.

Abstract

Neuroblastoma is a childhood malignancy originating from cells of the sympathetic nervous system, exhibiting a marked diversity in outcome, with spontaneous regression at one end of the spectrum and severe disease and death at the other end. Features associated with frequent recurrence, a poor prognosis, and high tumor stage are loss of heterozygosity in the distal region of chromosome 1p and amplification of the N-myc gene. Patched 2 is a novel homologue to the tumor suppressor gene Patched 1, and has been mapped to 1p32-34, a part of chromosome 1 frequently deleted in high stage neuroblastoma tumors. RT-PCR analysis of 9 neuroblastoma cell lines showed expression of both Patched 1 and 2. We analyzed 14, mainly high stage, neuroblastoma tumors for mutations in the Patched 2 gene with denaturing HPLC using the Wave DNA fragment analysis system. In four tumor samples variations were detected within the coding sequence, and two of them gave rise to amino-acid substitutions. These variations were, however, also detected in normal DNA from the respective patients. We conclude that Patched 2 is expressed, but not frequently mutated, in high stage neuroblastomas and is therefore not likely to be involved in the genesis of this tumor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Chromosomes, Human, Pair 1*
  • Humans
  • Membrane Proteins / genetics*
  • Mutation
  • Neuroblastoma / genetics*
  • Neuroblastoma / pathology
  • Patched Receptors
  • Patched-1 Receptor
  • Patched-2 Receptor
  • Receptors, Cell Surface

Substances

  • Membrane Proteins
  • PTCH1 protein, human
  • PTCH2 protein, human
  • Patched Receptors
  • Patched-1 Receptor
  • Patched-2 Receptor
  • Receptors, Cell Surface