In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemia

Genes Chromosomes Cancer. 1990 Nov;2(4):341-4. doi: 10.1002/gcc.2870020413.

Abstract

In situ hybridization was performed in a case of acute monoblastic leukemia (FAB type M5b) with a rearrangement of the long arm of chromosome 11. Cytogenetic analysis after R- and G-banding showed an apparent deletion of 11q with a breakpoint at 11q23, and a translocation t(6;11) was suspected in certain metaphases. In situ hybridization with a biotinylated cosmid probe hybridizing at 11q25 confirmed the translocation t(6;11)(q27;q23). Use of nonradioactive in situ hybridization techniques for more precise characterization of chromosomal rearrangements in malignant cells is emphasized.

Publication types

  • Case Reports

MeSH terms

  • Bone Marrow / ultrastructure
  • Child
  • Chromosome Banding
  • Chromosomes, Human, Pair 11*
  • Chromosomes, Human, Pair 6*
  • Cosmids
  • DNA, Neoplasm
  • Female
  • Humans
  • Karyotyping
  • Leukemia, Monocytic, Acute / genetics*
  • Nucleic Acid Hybridization
  • Translocation, Genetic*

Substances

  • DNA, Neoplasm