ECOTROPIC VIRUS INTEGRATIONS SITE-1 GENE PREFERENTIALLY EXPRESSED IN POST-MYELODYSPLASIA ACUTE MYELOID-LEUKEMIA - POSSIBLE ASSOCIATION WITHGATA-1, GATA-2, AND STEM-CELL LEUKEMIA GENE-EXPRESSION
Jh. Ohyashiki et al., ECOTROPIC VIRUS INTEGRATIONS SITE-1 GENE PREFERENTIALLY EXPRESSED IN POST-MYELODYSPLASIA ACUTE MYELOID-LEUKEMIA - POSSIBLE ASSOCIATION WITHGATA-1, GATA-2, AND STEM-CELL LEUKEMIA GENE-EXPRESSION, Blood, 85(12), 1995, pp. 3713-3718
We investigated expression of the human ecotropic virus integration si
te-1 (EVI1) gene in patients with leukemia and myelodysplastic syndrom
e (MDS) using the reverse transcriptase-polymerase chain reaction (RI-
PCR) method. The EVI1 transcripts were detected in 5 (10.0%) of 50 pat
ients with de novo acute myeloid leukemia (AML), including two AML pat
ients with trilineage myelodysplasia, and in 8 (34.8%) of 23 patients
with post-myelodysplastic syndrome AML (post-MDS AML). EVI1 expression
was also detected in 6 (35.3%) of 17 MDS patients and three of six pa
tients with chronic myeloid leukemia (CML) in myelomegakaryoblast cris
is. No EVI1 transcripts were detected in patients with acute lymphoid
leukemia (n = 15) or CML in lymphoid blast crisis (n = 4). Chromosomal
abnormalities at the 3q26 region, where the EVI1 gene is located, wer
e found in one patient with MDS and two patients with CML myelomegakar
yoblast crisis who had EVI1 expression. Our results showed that EVI1 e
xpression was frequent in patients with post-MDS AML and AML with tril
ineage myelodysplasia, regardless of the presence or absence of 3q26 a
bnormalities. EVI1 expression was accompanied by expression of GATA-1
and GATA-2 and often by stem cell leukemia (SCL) gene expression. In p
atients with post-MDS AML, EVI1 expression was not always associated w
ith a 3q26 abnormality, whereas EVI1 expression in CML myelomegakaryob
last crisis was often linked to a 3q26 abnormality. Our results sugges
t that the leukemogenic role of EVI1 expression may differ between pos
t-MDS AML and leukemia, with EVI1 expression associated with a 3q26 ab
normality. (C) 1995 by The American Society of Hematology.