Ovarian cancer cells polarize macrophages toward a tumor-associated phenotype

T Hagemann, J Wilson, F Burke, H Kulbe… - The Journal of …, 2006 - journals.aai.org
T Hagemann, J Wilson, F Burke, H Kulbe, NF Li, A Pluddemann, K Charles, S Gordon…
The Journal of Immunology, 2006journals.aai.org
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 …
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-α or its receptors revealed that TNF-α 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-α Abs or grown in TNF-α−/− mice. Chemical communication between tumor cells and macrophages may be important in regulating the cancer cytokine microenvironment.
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