Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2139058 | Leukemia Research | 2008 | 4 Pages |
Abstract
Approximately half of essential thrombocythemia (ET) patients and almost all with polycythemia vera (PV) bear the activating JAK2617V>F point mutation, which arises at the multipotent haemopoietic progenitor cell level. Although ET is mainly characterized by megacaryocyte proliferation, the cases that are positive for the JAK2617V>F mutation also show increased bone marrow cellularity and higher erythrocyte and granulocyte counts. After establishing short- and long-term bone marrow cultures we found that the frequency of committed haemopoietic progenitors in the bone marrow, was not increased in JAK2617V>F positive ET compared to the negative ones, whereas in long-term cultures (LTBMC) JAK2617V>F positive ET display a growth pattern more similar to that observed in LTBMC produced by PV marrow cells. Our data support the notion that JAK2617V>F positive ET and PV represents a continuum spectrum of alterations within the same disease.
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Authors
E. Spanoudakis, D. Margaritis, I. Kotsianidis, G. Georgiou, G. Tripsianis, A. Anastasiadis, A. Karakolios, D. Pantelidou, P. Panayiotidis, G. Bourikas, C. Tsatalas,