A new recurrent 9q34 duplication in pediatric T-cell acute lymphoblastic leukemia

Leukemia. 2006 Jul;20(7):1245-53. doi: 10.1038/sj.leu.2404247. Epub 2006 May 4.


Over the last decade, genetic characterization of T-cell acute lymphoblastic leukemia (T-ALL) has led to the identification of a variety of chromosomal abnormalities. In this study, we used array-comparative genome hybridization (array-CGH) and identified a novel recurrent 9q34 amplification in 33% (12/36) of pediatric T-ALL samples, which is therefore one of the most frequent cytogenetic abnormalities observed in T-ALL thus far. The exact size of the amplified region differed among patients, but the critical region encloses approximately 4 Mb and includes NOTCH1. The 9q34 amplification may lead to elevated expression of various genes, and MRLP41, SSNA1 and PHPT1 were found significantly expressed at higher levels. Fluorescence in situ hybridization (FISH) analysis revealed that this 9q34 amplification was in fact a 9q34 duplication on one chromosome and could be identified in 17-39 percent of leukemic cells at diagnosis. Although this leukemic subclone did not predict for poor outcome, leukemic cells carrying this duplication were still present at relapse, indicating that these cells survived chemotherapeutic treatment. Episomal NUP214-ABL1 amplification and activating mutations in NOTCH1, two other recently identified 9q34 abnormalities in T-ALL, were also detected in our patient cohort. We showed that both of these genetic abnormalities occur independently from this newly identified 9q34 duplication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 9*
  • Female
  • Gene Duplication*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Leukemia-Lymphoma, Adult T-Cell / genetics*
  • Male
  • Oncogene Proteins, Fusion / genetics
  • Predictive Value of Tests
  • Receptor, Notch1 / genetics
  • Recurrence
  • Reverse Transcriptase Polymerase Chain Reaction


  • NOTCH1 protein, human
  • NUP214-ABL1 fusion protein, human
  • Oncogene Proteins, Fusion
  • Receptor, Notch1