INCREASED EVI-1 EXPRESSION IS FREQUENTLY OBSERVED IN BLASTIC CRISIS OF CHRONIC MYELOCYTIC-LEUKEMIA

Citation
S. Ogawa et al., INCREASED EVI-1 EXPRESSION IS FREQUENTLY OBSERVED IN BLASTIC CRISIS OF CHRONIC MYELOCYTIC-LEUKEMIA, Leukemia, 10(5), 1996, pp. 788-794
Citations number
36
Categorie Soggetti
Hematology,Oncology
Journal title
ISSN journal
08876924
Volume
10
Issue
5
Year of publication
1996
Pages
788 - 794
Database
ISI
SICI code
0887-6924(1996)10:5<788:IEEIFO>2.0.ZU;2-S
Abstract
Evi-1 is a transforming gene originally identified in a common integra tion site of murine leukemia retrovirus and mapped in human chromosome 3q26. It is not normally expressed in either human or murine hematopo ietic cells, but is overexpressed in retrovirus-induced murine myeloid leukemias as well as human myeloid leukemias with 3q26 abnormalities, and thus thought to be responsible for both human and murine leukemog enesis. In this study, possible involvement of the Evi-1 gene in human leukemias was evaluated by Northern blot analysis in a total of 73 pa tients with various types of leukemias. We found that increased expres sion of the Evi-1 gene was most frequently observed in patients with C ML In blastic crisis, It was found in 10 of 14 (71.0%) samples from CM L in blastic crisis, three of 15(20.0%) from acute myelocytic leukemia , three of 11 (27.3%) from MDS-derived leukemia, and one of 11 (9.1%) from acute lymphoblastic leukemia. Among 18 patients showing increased Evi-1 expression, none of 17 informative patients showed cytogenetic abnormalities involving 3q26. In addition, Southern blot analysis reve aled neither amplification nor rearrangements of the Evi-1 gene in 11 Evi-1-positive patients whose DNA samples were available. Our results suggest that increased expression of the Evi-1 gene may play an import ant role in development of human leukemias, especially in progression from chronic phase to blastic crisis of CML even without 3q26 abnormal ities.