Activation of insulin-like growth factor I receptor signaling pathway is critical for mouse plasma cell tumor growth

Cancer Res. 2000 Jul 15;60(14):3909-15.

Abstract

Plasma cell neoplasia in humans generally occurs as multiple myeloma, an incurable form of cancer. Tumors with marked similarity can be induced in mice by a variety of agents, including chemicals, silicone, and oncogene-containing retroviruses, suggesting the use of murine tumors as an informative model to study plasma cell disease. Herein, we have focused on the role of insulin-like growth factor I receptor (IGF-IR) signaling in the development of plasma cell disease. The insulin receptor substrate 2/phosphatidylinositol 3'-kinase/p70S6K pathway was found to be either constitutively or IGF-I-dependently activated in all plasma cell tumors. Biological relevance was demonstrated in that plasma cell lines with up-regulated IGF-IR expression levels exhibited mitogenic responses to IGF-I. More importantly, expression of a dominant-negative mutant of IGF-IR in these lines strongly suppressed tumorigenesis in vivo. Taken together, these results demonstrate that up-regulation and activation of IGF-IR and the downstream signaling pathway involving insulin receptor substrate 2, phosphatidylinositol 3'-kinase, and p70S6K may play an important role in the development of a broad spectrum of plasma cell tumors.

MeSH terms

  • Animals
  • Culture Media, Serum-Free
  • Enzyme Activation
  • Female
  • Immunoblotting
  • Insulin Receptor Substrate Proteins
  • Intracellular Signaling Peptides and Proteins
  • Lymphoma, B-Cell / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Neoplasm Transplantation
  • Neoplasms, Experimental / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Plasmacytoma / chemically induced
  • Plasmacytoma / metabolism*
  • Precipitin Tests
  • Proto-Oncogene Proteins c-abl / metabolism
  • Proto-Oncogene Proteins c-myc / metabolism
  • Proto-Oncogene Proteins c-raf / metabolism
  • Receptor, IGF Type 1 / metabolism*
  • Receptor, IGF Type 1 / physiology*
  • Ribosomal Protein S6 Kinases / metabolism
  • Signal Transduction
  • Time Factors
  • Transfection
  • Tumor Cells, Cultured
  • Up-Regulation

Substances

  • Culture Media, Serum-Free
  • IRS2 protein, human
  • Insulin Receptor Substrate Proteins
  • Intracellular Signaling Peptides and Proteins
  • Irs2 protein, mouse
  • Phosphoproteins
  • Proto-Oncogene Proteins c-myc
  • Phosphatidylinositol 3-Kinases
  • Receptor, IGF Type 1
  • Proto-Oncogene Proteins c-abl
  • Proto-Oncogene Proteins c-raf
  • Ribosomal Protein S6 Kinases