Insulin-like growth factor-I-induced migration of melanoma cells is mediated by interleukin-8 induction

Cell Growth Differ. 2002 Feb;13(2):87-93.

Abstract

Successive events of growth factor-induced autocrine and paracrine activation promote tumor growth and metastasis. Insulin-like growth factor-I (IGF-I) stimulates melanoma cells to grow, survive, and migrate. Interleukin-8 (IL-8) is produced by melanoma cells and has been correlated with melanoma metastasis, but the biological functions of this cytokine have not been elucidated. We show here that IGF-I-induced migration of melanoma cells could be inhibited by neutralizing antibody against IL-8. IGF-I overexpression induced IL-8 production in melanoma cells, especially in biologically early melanomas by accelerating its transcription rate via activation of mitogen-activated protein kinase pathway. IGF-I treatment phosphorylated c-Jun and stimulated the binding of AP-1 but not NF-kappaB to the IL-8 promoter. These data identify IL-8 as a new target of IGF-I in melanoma and suggest that some of the biological functions of IGF-I are mediated by IL-8.

Publication types

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

MeSH terms

  • Antibodies, Monoclonal
  • Blotting, Northern
  • Blotting, Western
  • Cell Movement / drug effects*
  • Cell Nucleus / metabolism
  • DNA Primers / chemistry
  • Electrophoretic Mobility Shift Assay
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • In Vitro Techniques
  • Insulin / metabolism
  • Insulin-Like Growth Factor I / pharmacology*
  • Interleukin-8 / biosynthesis*
  • Melanoma / metabolism*
  • RNA, Messenger / metabolism
  • Tumor Cells, Cultured / drug effects*
  • Tumor Cells, Cultured / metabolism

Substances

  • Antibodies, Monoclonal
  • DNA Primers
  • Insulin
  • Interleukin-8
  • RNA, Messenger
  • Insulin-Like Growth Factor I