Ovarian cancer cells polarize macrophages toward a tumor-associated phenotype

J Immunol. 2006 Apr 15;176(8):5023-32. doi: 10.4049/jimmunol.176.8.5023.

Abstract

Tumor-associated macrophages (TAM) may have tumor-promoting activity, but it is not clear how their phenotype is achieved. In this study, we demonstrate that ovarian cancer cells switch cocultured macrophages to a phenotype similar to that found in ovarian tumors. Tumor cells caused dynamic changes in macrophage cytokine, chemokine, and matrix metalloprotease mRNA, and protein-inducing mediators that are found in human cancer. Macrophage mannose, mannose receptor, and scavenger receptors (SR-As) were also up-regulated by coculture, but not by conditioned medium. To further validate the model, we studied SR-A regulation on TAM in vitro and in vivo. Coculture of murine macrophages from mice deficient in TNF-alpha or its receptors revealed that TNF-alpha was key to SR-A induction via its p75 receptor. SR-A expression was also reduced in TAM from ovarian cancers treated with anti-TNF-alpha Abs or grown in TNF-alpha(-/-) mice. Chemical communication between tumor cells and macrophages may be important in regulating the cancer cytokine microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Communication
  • Cell Line, Tumor
  • Chemokines / biosynthesis
  • Chemokines / genetics
  • Coculture Techniques
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Female
  • Gene Expression
  • Humans
  • Lectins, C-Type / metabolism
  • Macrophage Activation
  • Macrophages / immunology*
  • Macrophages / physiology
  • Mannose Receptor
  • Mannose-Binding Lectins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Ovarian Neoplasms / immunology*
  • Ovarian Neoplasms / physiopathology
  • Phenotype
  • Receptors, Cell Surface / metabolism
  • Scavenger Receptors, Class A / metabolism
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / deficiency
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Chemokines
  • Cytokines
  • Lectins, C-Type
  • Mannose Receptor
  • Mannose-Binding Lectins
  • Receptors, Cell Surface
  • Scavenger Receptors, Class A
  • Tumor Necrosis Factor-alpha