Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: A complex chromosomal rearrangement of underestimated frequency in disease progression?

• Published in: Genes chromosomes & cancer 2008-12, Vol.47 (12), p.1110-1117
• Main Authors: Deluche, Lauréline, Joha, Sami, Corm, Sélim, Daudignon, Agnès, Geffroy, Sandrine, Quief, Sabine, Villenet, Céline, Kerckaert, Jean-Pierre, Laï, Jean-Luc, Preudhomme, Claude, Roche-Lestienne, Catherine
• Format: Article
• Language: English
• Subjects: Adult; Chromosomes, Human, Pair 21 - genetics; Core Binding Factor Alpha 2 Subunit - genetics; Disease Progression; DNA-Binding Proteins - genetics; Female; Gene Duplication; Humans; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics; Models, Genetic; Nucleic Acid Hybridization; Oncogene Proteins, Fusion - genetics; Oncogene Proteins, Fusion - metabolism; Protein Isoforms; Recombinant Fusion Proteins - genetics; Sequence Deletion; Transcription Factors - genetics; Translocation, Genetic; Tumor Cells, Cultured
• ISSN: 1045-2257; 1098-2264
• DOI: 10.1002/gcc.20611

Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by the presence in leukemic stem cells of the Philadelphia chromosome (Ph) and the formation of the BCR‐ABL1 fusion. Untreated, the disease progresses to accelerate phase and blast crisis in which hematopoietic differentiation has become arrested. CML progression is frequently associated with cytogenetic evidence of clonal evolution, defined as additional chromosomal aberrations. We here report a CML resistant to tyrosine kinase inhibitors that rapidly progressed to blastic phase. At this time, array CGH performed on CD34+ cells revealed cryptic partial deletions of both PRDM16 and RUNX1 and duplication of the der(21) chromosome. These genomic rearrangements were confirmed by FISH with probes targeting the deletion on chromosome 21 (24 kb), and with BAC probes flanking the deletion on 1p36 (220 kb). However, no cryptic t(1;21)(p36;q22) and/or RUNX1‐PRDM16 were detected, suggesting that these deletions are the residual hallmarks of a more complex mechanism of chromosomal rearrangement, as indicated by the additional inversion of the region bounded by 1p36.32 and 1p36.12 breaks. At the molecular level, these abnormalities lead to the overexpression of the PR‐domain negative oncogenic isoform of PRDM16, associated with two deleted copies within the runt domain of C‐teminal aberrant RUNX1. These events are not detectable by conventional cytogenetic and molecular strategies, and may be of underestimated frequency in disease progression. © 2008 Wiley‐Liss, Inc.