p53 gene mutation in the bone-marrow of a patient with diffuse mixed cell type lymphoma at diagnosis predicting eventual progression to large cell lymphoma

Leuk Lymphoma. 1998 Apr;29(3-4):415-21. doi: 10.3109/10428199809068578.

Abstract

Mutations of the p53 tumor suppressor gene have been used as molecular genetic markers of disease and serve as a prognostic indicator in various malignancies including non-Hodgkin's lymphoma (NHL). Alterations in the p53 gene were investigated in a bone marrow sample from a NHL patient admitted for autologous bone marrow transplantation. Diffuse mixed small and large cell NHL, was initially diagnosed which eventually progressed to large cell lymphoma at relapse following poly-chemotherapy. A sequential technique of polymerase chain reaction-mediated single-strand conformational polymorphism (PCR-SSCP) of the p53 gene revealed a shift in one band of exon 6 in the bone marrow, collected at the time of initial diagnosis. No mutations were detected in exons 5, 7, 8 and 9. Direct sequencing of exon 6 detected a single base change from G to C resulting in an amino acid substitution from glycine to histidine. Results of this study and data reviewed from other publications suggest that the missense p53 mutation seen in this patient at the time of diagnosis may perhaps have been used to predict the eventual outcome of the disease. This could, therefore, serve as an important genetic disease marker particularly in bone marrow or peripheral blood samples initially collected and cryopreserved for future possible autologous transplantation.

Publication types

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

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bone Marrow
  • Cisplatin / administration & dosage
  • Dexamethasone / administration & dosage
  • Disease Progression
  • Etoposide / administration & dosage
  • Fatal Outcome
  • Genes, p53 / genetics*
  • Genetic Markers
  • Humans
  • Ifosfamide / administration & dosage
  • Lymphoma, Large B-Cell, Diffuse / genetics*
  • Lymphoma, Non-Hodgkin / drug therapy
  • Lymphoma, Non-Hodgkin / genetics*
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Sequence Analysis, DNA

Substances

  • Genetic Markers
  • Etoposide
  • Dexamethasone
  • Cisplatin
  • Ifosfamide

Supplementary concepts

  • DICE protocol