Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia

Haematologica. 2006 Sep;91(9):1248-51.

Abstract

We developed dual-color split fluorescence in situ hybridization (FISH) assays to detect AF10 and/or CALM rearrangements. Among nine cases of acute leukemia with translocation breakpoints at 10p13 and 11q14-21, a CALM/AF10 rearrangement was found in seven and was confirmed by reverse transcriptase polymerase chain reaction (RT-PCR) in all. In 2/7 cases, FISH detected CALM/AF10 in extramedullary leukemic infiltrations in the mediastinum and breast. As expected, FISH was less sensitive than RT-PCR for disease monitoring of CALM-AF10 positive cases. This new FISH assay reliably discriminates between MLL/AF10 and CALM/AF10 genomic rearrangements, identifies variant and complex CALM/AF10 translocations and detects the CALM/AF10 rearrangement in extramedullary leukemic infiltrations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Child
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence / methods*
  • Leukemia / genetics*
  • Leukemia / pathology
  • Leukemic Infiltration / diagnosis
  • Male
  • Middle Aged
  • Oncogene Proteins, Fusion / genetics*
  • Retrospective Studies
  • Translocation, Genetic*

Substances

  • AF10-CALM fusion protein, human
  • Oncogene Proteins, Fusion