3q26/EVI1 rearrangements in myeloid hemopathies: a cytogenetic review

Author:

De Braekeleer Marc123,Le Bris Marie-Josée3,De Braekeleer Etienne45,Basinko Audrey23,Morel Frédéric123,Douet-Guilbert Nathalie123

Affiliation:

1. Laboratoire d'Histologie, Embryologie et Cytogénétique, Faculté de Médecine et des Sciences de la Santé, Université de Brest, Brest, France

2. Institut National de la Santé et de la Recherche Médicale (INSERM), U1078, Brest, France

3. Service de Cytogénétique et Biologie de la Reproduction, Hôpital Morvan, CHRU Brest, Brest, France

4. Division of Stem Cells & Cancer, German Cancer Research Center (DKFZ) & Heidelberg Institute for Stem Cell Technology & Experimental Medicine GmbH (HI-STEM), Heidelberg, Germany

5. Haematological Cancer Genetics, Wellcome Trust Sanger Institute, Cambridge, UK

Abstract

ABSTRACT  The EVI1 gene, located in chromosomal band 3q26, is a transcription factor that has stem cell-specific expression pattern and is essential for the regulation of self-renewal of hematopoietic stem cells. It is now recognized as one of the dominant oncogenes associated with myeloid leukemia. EVI1 overexpression is associated with minimal to no response to chemotherapy and poor clinical outcome. Several chromosomal rearrangements involving band 3q26 are known to induce EVI1 overexpression. They are mainly found in acute myeloid leukemia and blastic phase of Philadelphia chromosome-positive chronic myeloid leukemia, more rarely in myelodysplastic syndromes. They include inv(3)(q21q26), t(3;3)(q21;q26), t(3;21)(q26;q22), t(3;12)(q26;p13) and t(2;3)(p15–23;q26). However, many other chromosomal rearrangements involving 3q26/EVI1 have been identified. The precise molecular event has not been elucidated in the majority of these chromosomal abnormalities and most gene partners remain unknown.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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