Identification of Two Critically Deleted Regions within Chromosome Segment 7q35-q36 in EVI1 Deregulated Myeloid Leukemia Cell Lines |
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| Authors: | An De Weer Bruce Poppe Sarah Vergult Pieter Van Vlierberghe Marjan Petrick Robrecht De Bock Yves Benoit Lucien Noens Anne De Paepe Nadine Van Roy Bj?rn Menten Frank Speleman |
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| Affiliation: | 1. Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; 2. Department of Radiotherapy, Oncology and Hematology, AZ Sint-Lucas, Ghent, Belgium.; 3. Department of Hematology, ZNA Middelheim, Antwerp, Belgium.; 4. Department of Pediatric Hemato-Oncology, Ghent University Hospital, Ghent, Belgium.; 5. Department of Hematology, Ghent University Hospital, Ghent, Belgium.;Innsbruck Medical University, Austria |
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| Abstract: | Chromosomal rearrangements involving the EVI1 proto-oncogene are a recurrent finding in myeloid leukemias and are indicative of a poor prognosis. Rearrangements of the EVI1 locus are often associated with monosomy 7 or cytogenetic detectable deletions of part of 7q. As EVI1 overexpression alone is not sufficient to induce leukemia, loss of a 7q tumour suppressor gene might be a required cooperating event. To test this hypothesis, we performed high-resolution array comparative genomic hybridization analysis of twelve EVI1 overexpressing patients and three EVI1 deregulated cell lines to search for 7q submicroscopic deletions. This analysis lead to the delineation of two critical regions, one of 0.39 Mb on 7q35 containing the CNTNAP2 gene and one of 1.33 Mb on chromosome bands 7q35–q36 comprising nine genes in EVI1 deregulated cell lines. These findings open the way to further studies aimed at identifying the culprit EVI1 implicated tumour suppressor genes on 7q. |
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