Mutations in the Wilms' tumor gene WT1 in leukemias

Blood. 1996 Mar 15;87(6):2171-9.

Abstract

The tissue-specific Wilms' tumor gene WT1 is expressed in a range of acute leukemias and hematopoietic cell lines. Using single-strand conformational polymorphism analysis, we have found mutations in the WT1 gene in 4 of 36 acute leukemias. WT1 mutations are found in 15% of cases of acute myeloid leukemia, in which they are associated with a poor response to chemotherapy. The mutations comprise small insertions in exons 1 and 7 and a nonsense mutation in exon 9. All are predicted to produce a truncated WT1 protein with absence or disruption of the zinc finger region. These are the first mutations in the WT1 gene to be described in sporadic leukemia.

Publication types

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

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Amino Acid Sequence
  • Base Sequence
  • Cells, Cultured
  • Child
  • DNA Mutational Analysis
  • DNA, Neoplasm / genetics*
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics
  • Exons / genetics
  • Fatal Outcome
  • Female
  • Genes, Wilms Tumor*
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • Leukemia / classification
  • Leukemia / genetics*
  • Leukemia / mortality
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Polymorphism, Single-Stranded Conformational
  • Prognosis
  • RNA, Neoplasm / genetics
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics
  • WT1 Proteins
  • Zinc Fingers / genetics

Substances

  • DNA, Neoplasm
  • DNA-Binding Proteins
  • RNA, Neoplasm
  • Transcription Factors
  • WT1 Proteins

Associated data

  • GENBANK/S82032