NPM/ALK downregulates p27Kip1 in a PI-3K-dependent manner

Exp Hematol. 2004 Dec;32(12):1265-71. doi: 10.1016/j.exphem.2004.11.002.

Abstract

Objectives: Anaplastic large-cell lymphomas (ALCL) are frequently associated with the chromosomal translocation t(2;5) (p23;q35) resulting in the NPM/ALK fusion gene that encodes a constitutively activated tyrosine kinase. We showed that NPM/ALK stimulated cell proliferation and that PI-3K/AKT pathway played an important role in this effect. p27Kip1 is a member of the CDK family inhibitory proteins regulating the entry into S phase. It was reported that p27Kip1 function is impaired in many tumors. In this study we investigated the role of PI-3K/AKT in NPM/ALK-dependent downregulation of p27Kip1 protein.

Materials and methods: To investigate this phenomenon the pro-B cell line BaF3, BaF3 cell line stably expressing NPM/ALK, and ALCL SUP-M2 cell line were used. The p27Kip1 protein expression before and after LY294002, wortmannin, or epoxomicin treatment and phosphorylation status of AKT were measured in parental and NPM/ALK+ cells by Western analysis. Also, the localization of p27Kip1 protein was analyzed by fractionation and immunoblotting.

Results: p27Kip1 was found to be downregulated in NPM/ALK-transformed hematopoietic cells, but inhibition of proteasome-dependent degradation pathway by epoxomicin reversed this effect. In addition, treatment of NPM/ALK+ cells with LY294002, the PI-3K inhibitor, caused elevation of p27Kip1 protein expression and its nuclear localization.

Conclusions: Taken together, we postulate that NPM/ALK-PI-3K pathway stimulates cell proliferation by regulation of the expression and nuclear localization of p27Kip1.

Publication types

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

MeSH terms

  • B-Lymphocytes / cytology
  • B-Lymphocytes / metabolism
  • B-Lymphocytes / pathology
  • Blotting, Western
  • Carrier Proteins / metabolism*
  • Cell Line, Transformed
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Cell Proliferation / drug effects
  • Cell Transformation, Neoplastic / genetics
  • Chromones / pharmacology
  • Cyclin-Dependent Kinase Inhibitor p27
  • Down-Regulation* / drug effects
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation, Leukemic* / drug effects
  • Hematopoietic Stem Cells / metabolism
  • Hematopoietic Stem Cells / pathology
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Lymphoma, Large B-Cell, Diffuse / genetics*
  • Lymphoma, Large B-Cell, Diffuse / metabolism*
  • Lymphoma, Large B-Cell, Diffuse / pathology
  • Morpholines / pharmacology
  • Oligopeptides / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphorylation / drug effects
  • Proteasome Endopeptidase Complex / metabolism
  • Protein Transport / drug effects
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / metabolism*
  • S Phase / drug effects
  • S Phase / genetics
  • Signal Transduction / drug effects
  • Transformation, Genetic
  • Translocation, Genetic / genetics

Substances

  • CDKN1B protein, human
  • Carrier Proteins
  • Chromones
  • Enzyme Inhibitors
  • Intracellular Signaling Peptides and Proteins
  • Morpholines
  • Oligopeptides
  • Cyclin-Dependent Kinase Inhibitor p27
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Phosphatidylinositol 3-Kinases
  • p80(NPM-ALK) protein
  • Protein-Tyrosine Kinases
  • Proteasome Endopeptidase Complex
  • epoxomicin