Complex chromosomal rearrangements leading toMECOMoverexpression are recurrent in myeloid malignancies with various 3q abnormalities
Autor: | Giulia Marzocchi, Carmela Gurrieri, Elisa Zuffa, Gaia Ameli, Maria Antonella Bardi, Cristina Papayannidis, Rossella Paolini, Nicoletta Testoni, Giovanni Martinelli, Simona Luatti, Laura Bonaldi, Michele Cavo, Antonio Cuneo, Emanuela Ottaviani, Gian Matteo Rigolin, Carmen Baldazzi |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Cancer Research Myeloid MECOM medicine.diagnostic_test Breakpoint Myeloid leukemia Chromosomal translocation Biology medicine.disease 03 medical and health sciences Leukemia 030104 developmental biology 0302 clinical medicine medicine.anatomical_structure 030220 oncology & carcinogenesis Gene duplication Genetics Cancer research medicine Fluorescence in situ hybridization |
Zdroj: | Genes, Chromosomes and Cancer. 55:375-388 |
ISSN: | 1045-2257 |
Popis: | Chromosomal rearrangements involving 3q26 are recurrent findings in myeloid malignancies leading to MECOM overexpression, which has been associated with a very poor prognosis. Other 3q abnormalities have been reported and cryptic MECOM rearrangements have been identified in some cases. By fluorescence in situ hybridization (FISH) analysis, we investigated 97 acute myeloid leukemia/myelodysplastic syndrome patients with various 3q abnormalities to determine the role and the frequency of the involvement of MECOM. We identified MECOM rearrangements in 51 patients, most of them showed 3q26 involvement by chromosome banding analysis (CBA): inv(3)/t(3;3) (n = 26) and other balanced 3q26 translocations (t(3q26)) (n = 15); the remaining cases (n = 10) showed various 3q abnormalities: five with balanced translocations involving 3q21 or 3q25; two with homogenously staining region (hsr) on 3q; and three with other various 3q abnormalities. Complex rearrangements with multiple breakpoints on 3q, masking 3q26 involvement, were identified in cases with 3q21/3q25 translocations. Furthermore, multiple breaks were observed in two cases with t(3q26), suggesting that complex rearrangement may also occur in apparently simple t(3q26). Intrachromosomal gene amplification was another mechanism leading to MECOM overexpression in two cases with hsr on 3q. In the last three cases, FISH analysis revealed 3q26 involvement that was missed by CBA because of metaphases' suboptimal quality. All cases with MECOM rearrangements showed overexpression by real-time quantitative PCR. Finally, MECOM rearrangements can occur in patients with 3q abnormalities even in the absence of specific 3q26 involvement, underlining that their frequency is underestimated. As MECOM rearrangement has been associated with very poor prognosis, its screening should be performed in patients with any 3q abnormalities. |
Databáze: | OpenAIRE |
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