1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines

Genes Chromosomes Cancer. 1994 Jun;10(2):103-14. doi: 10.1002/gcc.2870100205.

Abstract

We report on the finding of a t(1;17) in two primary neuroblastomas. Subsequent fluorescence in situ hybridization (FISH) analysis revealed the presence of 1;17 translocations in four out of nine neuroblastoma cell lines. The chromosome 1 short arm breakpoints were determined using region-specific probes. FISH screening also demonstrated or confirmed the presence of 11;17 translocations in three cell lines and other chromosome 17 rearrangements in those cell lines that did not carry a t(1;17) or t(11;17). Our data extend previous cytogenetic findings and suggest that, in addition to the known involvement of chromosome 1, one or more genes on chromosome 17 also play a role in neuroblastoma development.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Gland Neoplasms / genetics
  • Adrenal Gland Neoplasms / pathology
  • Adrenal Gland Neoplasms / secondary
  • Bone Marrow / pathology
  • Bone Neoplasms / genetics
  • Bone Neoplasms / pathology
  • Bone Neoplasms / secondary
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / pathology
  • Cell Line
  • Child, Preschool
  • Chromosome Aberrations*
  • Chromosome Banding
  • Chromosome Disorders*
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 17*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Male
  • Neuroblastoma / genetics*
  • Neuroblastoma / pathology
  • Neuroblastoma / secondary
  • Translocation, Genetic*
  • Tumor Cells, Cultured