Abstract
NUP98 is among the most promiscuously translocated genes in hematological diseases. Among the 28 known fusion partners, there are two categories: homeobox genes and non-homeobox genes. The homeobox fusion partners are well-studied in animal models, resulting in HoxA cluster overexpression and hematological disease. The non-homeobox fusion partners are less well studied. We created transgenic animal models for three NUP98 fusion genes (one homeobox, two non-homeobox), and show that in this system, the NUP98-homeobox fusion promotes self-renewal and aberrant gene expression to a significantly greater extent. We conclude that homeobox partners create more potent NUP98 fusion oncogenes than do non-homeobox partners.
Original language | English |
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Pages (from-to) | 1668-1673 |
Number of pages | 6 |
Journal | Leukemia Research |
Volume | 37 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2013 |
Keywords
- Homeobox
- HOX
- Leukemia
- NUP98
- Translocation