Absence of the t(2;5) in Hodgkin's disease

Blood. 1995 May 15;85(10):2845-7.

Abstract

The cytogenetics of Hodgkin's disease (HD) is poorly understood. However, a t(2;5) is a common finding in CD30+ anaplastic large cell lymphoma (ALCL), a neoplasm thought by some to be closely related to HD. Recently, the t(2;5) has been cloned and found to represent fusion of the NPM gene with the ALK gene. Using Southern blot hybridization, one group has reported finding rearrangements of NPM in a proportion of cases of both ALCL and HD. In the current study, we used a highly sensitive reverse transcriptase-polymerase chain reaction methodology to analyze 34 cases of HD for the t(2;5). We were unable to find polymerase chain reaction evidence for the t(2;5) in any of the cases of HD, a result significantly different from our previous study of CD30+ non-Hodgkin's lymphomas (P < .02) including ALCL (P < .04), using identical methods. Our results do not support the hypothesis that the t(2;5) represents a common chromosomal abnormality for both HD and ALCL.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anaplastic Lymphoma Kinase
  • Base Sequence
  • Chromosome Aberrations / pathology
  • Chromosome Disorders
  • Chromosomes, Human, Pair 2
  • Chromosomes, Human, Pair 5
  • DNA Primers / chemistry
  • Gene Expression
  • Hodgkin Disease / genetics*
  • Humans
  • Molecular Sequence Data
  • Nuclear Proteins / genetics*
  • Nucleophosmin
  • Protein-Tyrosine Kinases / genetics*
  • RNA, Messenger / genetics
  • RNA, Neoplasm / genetics
  • Receptor Protein-Tyrosine Kinases
  • Translocation, Genetic

Substances

  • DNA Primers
  • Nuclear Proteins
  • RNA, Messenger
  • RNA, Neoplasm
  • Nucleophosmin
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • Protein-Tyrosine Kinases
  • Receptor Protein-Tyrosine Kinases