Tyrosine kinase mutations of JAK2 are rare events in AML but influence prognosis of patients with CBF-leukemias

Haematologica. 2007 Jan;92(1):137-8. doi: 10.3324/haematol.10489.

Abstract

We investigated a large number of acute myeloid leukemia (AML) samples (n=959) for the presence of the JAK2 V617F mutation. We found a low incidence of the mutation in these AML samples (1%). JAK2 V617F mutations clustered in AML samples with an aberrant karyotype (p<0.05). The incidence of JAK2 V617F in patients with a core binding factor (CBF) leukemia was 3.6% (p<0.01). Moreover, JAK2 V617F mutations in CBF leukemias were associated with an aggressive clinical course with 80% of the patients relapsing.

Publication types

  • Letter

MeSH terms

  • Aged
  • Cell Transformation, Neoplastic
  • Core Binding Factors / genetics*
  • Cytogenetics
  • Gene Expression Regulation, Leukemic*
  • Humans
  • Janus Kinase 2 / genetics*
  • Leukemia / genetics*
  • Leukemia, Myeloid, Acute / genetics*
  • Leukocyte Count
  • Middle Aged
  • Mutation*
  • Prognosis*

Substances

  • Core Binding Factors
  • JAK2 protein, human
  • Janus Kinase 2