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Primary malignant lymphoma of the brain: mutation pattern of rearranged immunoglobulin heavy chain gene.

Authors
  • Endo, Sumio1
  • Zhang, Shu-Jing
  • Saito, Takafumi
  • Kouno, Mitsuo
  • Kuroiwa, Toshihiko
  • Washiyama, Kazuo
  • Kumanishi, Toshiro
  • 1 Molecular Neuropathology, Brain Research Institute, Niigata University, Niigata 951-8585, Japan. , (Japan)
Type
Published Article
Journal
Japanese journal of cancer research : Gann
Publication Date
December 2002
Volume
93
Issue
12
Pages
1308–1316
Identifiers
PMID: 12495470
Source
Medline
License
Unknown

Abstract

Using reverse transcription-polymerase chain reaction (RT-PCR), six primary brain lymphomas, pathologically diagnosed as diffuse large B-cell lymphoma, were examined for rearranged VH-D-JH sequences of the immunoglobulin heavy chain gene, focusing on somatic mutations and intraclonal heterogeneity. The reliability of the isolated PCR clones was confirmed by in situ hybridization (ISH) with complementarity-determining region (CDR) 3 oligonucleotide probes. Sequence analysis of the PCR clones revealed a high frequency of somatic mutation, ranging from 8.8 to 27.3% (mean 18.2%) in the VH gene segments in all the lymphomas. A significantly lower frequency of replacement (R) mutations than expected was also seen in their frameworks (FRs) in all cases. These findings suggested that the precursor cells were germinal center (GC)-related cells in these lymphomas. However, despite extensive cloning experiments, intraclonal heterogeneity was not detected in any case except for one in which it could not be ruled out. Thus, it seemed likely that all of our brain lymphomas were derived from GC-related cells and that at least most of them were from post-GC cells.

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