Constitutive activation of STAT5 by the BCR-ABL oncogene in chronic myelogenous leukemia

Oncogene. 1996 Jul 18;13(2):247-54.

Abstract

Using chronic myelogenous leukemia (CML) as a model, we tested the hypothesis that cytokine-independent growth of leukemia cells results from aberrant activation of cytokine signaling pathways. The STAT5 (signal transducer and activator of transcription) protein, which is activated transiently in normal myeloid cells by cytokines such as GM-CSF (granulocyte-macrophage colony stimulating factor), was constitutively activated in cell lines derived from CML patients, even in the absence of GM-CSF. STAT5 was also activated in primary mouse bone marrow cells acutely transformed by the CML-specific BCR-ABL oncogene, but not by the serine kinase oncogene v-MOS. Reconstitution experiments in non-hematopoietic cells show that STAT5 activation by BCR-ABL occurs independent of cytokines. Results using BCR-ABL mutants which specifically uncouple connections to known signal transduction pathways show that STAT5 activation is kinase dependent and correlates directly with ability to confer cytokine independent growth in hematopoietic cells. BCR-ABL also activates JAK kinases, which may provide a mechanism for STAT activation. These findings are consistent with a role for STAT5 in hematopoietic transformation by BCR-ABL.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Bone Marrow / pathology
  • Bone Marrow / physiology
  • Bone Marrow Cells
  • Cell Division / physiology
  • Cell Transformation, Neoplastic
  • Cytokines / biosynthesis
  • DNA-Binding Proteins / physiology*
  • Enzyme Activation
  • Fusion Proteins, bcr-abl / genetics
  • Fusion Proteins, bcr-abl / physiology*
  • Humans
  • Janus Kinase 1
  • Janus Kinase 2
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / physiopathology*
  • Mice
  • Milk Proteins*
  • Molecular Sequence Data
  • Mutation
  • Protein-Tyrosine Kinases / metabolism
  • Proto-Oncogene Proteins*
  • STAT5 Transcription Factor
  • Signal Transduction / physiology
  • Trans-Activators / physiology*
  • Tumor Cells, Cultured

Substances

  • Cytokines
  • DNA-Binding Proteins
  • Milk Proteins
  • Proto-Oncogene Proteins
  • STAT5 Transcription Factor
  • Trans-Activators
  • Protein-Tyrosine Kinases
  • Fusion Proteins, bcr-abl
  • JAK1 protein, human
  • JAK2 protein, human
  • Jak1 protein, mouse
  • Jak2 protein, mouse
  • Janus Kinase 1
  • Janus Kinase 2