Infrequent mutations in the P53 gene in primary human T-cell acute lymphoblastic leukemia

Leukemia. 1991 Oct;5(10):839-40.

Abstract

Alterations of the P53 tumor suppressor gene are present in various human malignancies. P53 mutations have recently been detected in 60% of human T-cell leukemia permanent cell lines. To determine the frequency of P53 mutations in primary T-cell acute lymphoblastic leukemia (T-ALL), a powerful method for the detection of structural alterations of DNA was used, namely, single-strand conformation polymorphism analysis of DNA fragments amplified by the polymerase chain reaction. No point mutation in the P53 gene was shown in any of the 30 T-ALL patients tested. Unlike T-cell leukemia permanent cell lines, P53 mutations are uncommon in T-ALL.

MeSH terms

  • Base Sequence
  • Chromosomes, Human, Pair 17 / physiology
  • DNA, Neoplasm / analysis
  • DNA, Neoplasm / genetics
  • DNA, Single-Stranded / analysis
  • DNA, Single-Stranded / genetics
  • Genes, p53 / genetics*
  • Humans
  • Leukemia-Lymphoma, Adult T-Cell / genetics*
  • Molecular Sequence Data
  • Mutation
  • Polymerase Chain Reaction / methods
  • Polymorphism, Genetic
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*

Substances

  • DNA, Neoplasm
  • DNA, Single-Stranded