p53 mutations in hairy cell leukemia

Leukemia. 2000 Apr;14(4):706-11. doi: 10.1038/sj.leu.2401721.

Abstract

We have studied the frequency of p53 mutations in genomic DNA extracted from peripheral blood or the spleen of 61 patients with hairy cell leukemia using PCR-SSCP and automated cycle sequencing. We identified exon 5-8 mutations in 17 cases, corresponding to a frequency of 28%. In four cases, mutations were localized in exon 5; one patient with atypical HCL had a mutation in exon 6 at the 3' boundary; five cases showed mutations in exon 7, while exon 8 was found to be mutated in seven cases. The mutations found could be divided into three major categories: structural (n=9), inactivating (n= 6), and neutral (n= 2) mutations. None of the three transitions found occurred at CpG dinucleotides. The rate of p53 mutations found in this large cohort of HCL patients is unexpectedly high as in other non-Hodgkin lymphomas p53 mutations predict for poor treatment outcome. The character of the mutations we have found is entirely different from that described in other hematologic malignancies.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Amino Acid Substitution
  • Cell Cycle
  • Codon
  • Cohort Studies
  • CpG Islands
  • DNA Mutational Analysis
  • DNA, Neoplasm / blood
  • DNA, Neoplasm / genetics
  • Female
  • Genes, p53*
  • Humans
  • Leukemia, Hairy Cell / genetics*
  • Leukemia, Hairy Cell / mortality
  • Leukemia, Hairy Cell / pathology
  • Lymphoma, Non-Hodgkin / genetics
  • Lymphoma, Non-Hodgkin / mortality
  • Male
  • Middle Aged
  • Mutation*
  • Point Mutation
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Prognosis
  • Sequence Deletion
  • Spleen / chemistry

Substances

  • Codon
  • DNA, Neoplasm