ALL-1 gene at chromosome 11q23 is consistently altered in acute leukemia of early infancy

Blood. 1993 Jul 15;82(2):544-6.

Abstract

Early infancy (< 1 year of age), massive tumor cell burden, and extremely poor prognosis are characteristic features of a particular subset of childhood acute leukemias (AL). In these cases, chromosome aberrations at the 11q23 band are the most frequently reported cytogenetic abnormalities. We have recently cloned a genetic locus named ALL-1, in which DNA breakpoints are clustered in leukemic patients with 11q23 aberrations. Analysis of the ALL-1 genomic configuration in DNA from 15 infants with AL showed specific ALL-1 rearrangements in 12 cases (80%), including 5 with normal karyotypes. These findings indicate that a consistent genetic defect underlies this particular leukemic subset.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 11*
  • DNA, Neoplasm / genetics
  • Deoxyribonuclease BamHI
  • Deoxyribonuclease HindIII
  • Female
  • Gene Rearrangement
  • Humans
  • Infant
  • Karyotyping
  • Leukemia / genetics*
  • Male
  • Restriction Mapping

Substances

  • DNA, Neoplasm
  • Deoxyribonuclease BamHI
  • Deoxyribonuclease HindIII