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Leukemia ; 24(7): 1290-8, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20508609

RESUMO

Transformation to acute leukemia is a major complication of myeloproliferative neoplasms (MPNs), however, the genetic changes leading to transformation remain largely unknown. We screened nine patients with post-MPN leukemia for chromosomal aberrations using microarray karyotyping. Deletions on the short arm of chromosome 7 (del7p) emerged as a recurrent defect. We mapped the common deleted region to the IKZF1 gene, which encodes the transcription factor Ikaros. We further examined the frequency of IKZF1 deletions in a total of 29 post-MPN leukemia and 526 MPN patients without transformation and observed a strong association of IKZF1 deletions with post-MPN leukemia in two independent cohorts. Patients with IKZF1 loss showed complex karyotypes, and del7p was a late event in the genetic evolution of the MPN clone. IKZF1 deletions were observed in both undifferentiated and differentiated myeloid cell types, indicating that IKZF1 loss does not cause differentiation arrest but rather renders progenitors susceptible to transformation, most likely through chromosomal instability. Induced Ikzf1 haploinsufficiency in primary murine progenitors resulted in elevated Stat5 phosphorylation and increased cytokine-dependent growth, suggesting that reduced expression of IKZF1 is sufficient to perturb growth regulation. Thus, IKZF1 loss is an important step in the leukemic transformation of a subpopulation of MPN patients.


Assuntos
Cromossomos Humanos Par 7/genética , Deleção de Genes , Fator de Transcrição Ikaros/genética , Transtornos Mieloproliferativos/genética , Animais , Biomarcadores Tumorais/genética , Biomarcadores Tumorais/metabolismo , Células Cultivadas , Dosagem de Genes , Perfilação da Expressão Gênica , Humanos , Janus Quinase 2/genética , Perda de Heterozigosidade , Camundongos , Camundongos Endogâmicos C57BL , Mutação/genética , Análise de Sequência com Séries de Oligonucleotídeos , Fosforilação , Reação em Cadeia da Polimerase , RNA Mensageiro/genética , Receptores de Trombopoetina/genética , Fator de Transcrição STAT5/genética , Células-Tronco/metabolismo
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