Quantitative comparison of the expression of EVI1 and its presumptive antagonist, MDS1/EVI1, in patients with myeloid leukemia

Genes Chromosomes Cancer. 2003 Jan;36(1):80-9. doi: 10.1002/gcc.10144.

Abstract

The EVI1 gene in chromosome band 3q26 exhibits a number of properties consistent with a role as an oncogene, and its expression is activated in most myeloid leukemia patients with, as well as in a minority of patients without, 3q26 rearrangements. A splice variant of this gene, MDS1/EVI1, acts as its antagonist at least in some tissue culture assays. We established real-time quantitative reverse transcriptase polymerase chain reaction (RTQ-RT-PCR) assays for these mRNA variants to compare their expression levels in a quantitatively reliable manner. EVI1 was overexpressed to highly variable extents in all patients with, as well as in 14% of patients without, 3q26 rearrangements. In some of these samples, MDS1/EVI1 was also transcribed at elevated levels compared to those of healthy controls. However, although the induction of MDS1/EVI1 was comparable to, or higher than, that of EVI1 in three of five samples with a normal EVI1 locus, this was true for only two of 13 patients with a 3q26 aberration. We further provide preliminary evidence that the RTQ-RT-PCR assay may be useful for disease monitoring in patients overexpressing EVI1.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alternative Splicing / genetics
  • Child
  • Chromosome Aberrations
  • Chromosome Banding
  • Chromosomes, Human, Pair 3 / genetics
  • Cyclophilins / genetics
  • DNA-Binding Proteins / antagonists & inhibitors*
  • DNA-Binding Proteins / biosynthesis*
  • DNA-Binding Proteins / genetics
  • Disease Progression
  • Female
  • Humans
  • K562 Cells
  • Leukemia, Myeloid / genetics
  • Leukemia, Myeloid / metabolism*
  • Leukemia, Myeloid / pathology
  • MDS1 and EVI1 Complex Locus Protein
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Oncogene Proteins, Fusion*
  • Proto-Oncogenes*
  • Recombinant Fusion Proteins / biosynthesis*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / physiology*
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Transcription Factors / antagonists & inhibitors
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics
  • Tumor Cells, Cultured
  • U937 Cells

Substances

  • DNA-Binding Proteins
  • MDS1 and EVI1 Complex Locus Protein
  • MDS1-EVI1 fusion protein, human
  • MECOM protein, human
  • Oncogene Proteins, Fusion
  • Recombinant Fusion Proteins
  • Transcription Factors
  • Cyclophilins

Associated data

  • GENBANK/AF487422
  • GENBANK/AF487423
  • GENBANK/AF487424