ESTABLISHMENT OF A NOVEL HUMAN MYELOID-LEUKEMIA CELL-LINE (FKH-1) WITH T(6-9)(P23-Q34) AND THE EXPRESSION OF DEK-CAN CHIMERIC TRANSCRIPT

Citation
H. Hamaguchi et al., ESTABLISHMENT OF A NOVEL HUMAN MYELOID-LEUKEMIA CELL-LINE (FKH-1) WITH T(6-9)(P23-Q34) AND THE EXPRESSION OF DEK-CAN CHIMERIC TRANSCRIPT, British Journal of Haematology, 102(5), 1998, pp. 1249-1256
Citations number
30
Categorie Soggetti
Hematology
ISSN journal
00071048
Volume
102
Issue
5
Year of publication
1998
Pages
1249 - 1256
Database
ISI
SICI code
0007-1048(1998)102:5<1249:EOANHM>2.0.ZU;2-S
Abstract
Translocation t(6;9)(p23;q34), resulting in a dek-can gene fusion, is a recurrent chromosomal abnormality mainly associated with specific su btypes of acute myeloid leukaemia (AML) and myelodysplastic syndrome ( MDS). Patients with this type of chromosomal change are usually young and their prognosis is poor. The role of fusion protein generated from dek-can chimaeric transcript on the leukaemogenesis of t(6;9) AML or MDS is as yet unknown. We have established the first permanent cell li ne (FKH-1) with t(6;9), derived from the peripheral blood of a patient with t(6;9) AML transformed from Philadelphia chromosome (Phl)negativ e chronic myelocytic leukaemia (CML). The FKH-1 expressed myelomonocyt ic markers and dek-can chimaeric transcript, In the presence of 10 ng/ ml recombinant human granulocyte colony-stimulating factor (G-CSF), th e cells doubled every 54h and showed multilineage myeloid differentiat ion,; resulting in heterogenous morphologies such as macrophages, baso phils, eosinophils and neutrophils. Thus, this cell line may be derive d from a pluripotent myeloid stem cell and should be a useful tool for biomolecular studies on the pathogenesis of t(6;9) myeloid malignanci es which have rarely been investigated because of the lack of continuo usly proliferating cells.