Absence of mutations in the NBS1 gene in B-cell malignant lymphoma patients

Anticancer Res. 2000 May-Jun;20(3B):1897-900.

Abstract

Background: Nijmegen breakage syndrome (NBS), also known as ataxia-telangiectasia (AT) variant, is an autosomal recessive disorder characterized by microcephaly, growth retardation, severe combined immunodeficiency and a high incidence of lymphoid carcinoma, the majority of which are B-cell lymphomas. To determine whether the NBS1 gene is a tumor suppressor gene in B-cell lymphoma, we screened B-cell malignant lymphoma (ML) for any evidence of NBS1 mutation.

Materials and methods: Sequence analysis of the NBS1 gene was performed from PCR products amplified from the DNA of 12 extracranial ML or RT-PCR products amplified from cDNA of 8 primary central nervous system lymphoma.

Results: Direct sequence analysis revealed that no NBS1 mutations were present in any of these patients.

Conclusion: The present results suggested that the contribution of NBS1 mutations to B-cell ML was minimal, despite the fact that the NBS1 gene was causative factor in these cases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Brain Neoplasms / genetics
  • Child
  • Child, Preschool
  • Codon / genetics
  • DNA Mutational Analysis
  • DNA, Neoplasm / genetics*
  • Genes, Recessive
  • Genes, Tumor Suppressor
  • Humans
  • Infant
  • Lymphoma, B-Cell / genetics*
  • Neoplasm Proteins / genetics*
  • Neoplastic Syndromes, Hereditary / genetics*
  • Nuclear Proteins / genetics*
  • Polymorphism, Genetic
  • Polymorphism, Single-Stranded Conformational
  • Radiation Tolerance / genetics
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Codon
  • DNA, Neoplasm
  • Neoplasm Proteins
  • Nuclear Proteins