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Experimental Therapeutics, Preclinical Pharmacology |
Breast Oncology and Department of Pathology, Tokyo Metropolitan Komagome Hospital, 3-18-22, Honkomagome, Bunkyo-ku, Tokyo 113, Japan [T. U., M. T., H. S., M. M., H. B., K. K., M. K.], and Department of Molecular Preventive Medicine, School of Medicine, Tokyo University, Tokyo, Japan [H. I., K. M.]
Tumor cells stimulate the formation of stroma that secretes
various mediators pivotal for tumor growth, including growth factors,
cytokines, and proteases. However, little is known about the local
regulation of these soluble mediators in the human tumor
microenvironment. In this study, the local expression of cytokines,
chemokines, and angiogenic factors was investigated in primary breast
cancer tissue. The concentrations of interleukin (IL)-1, IL-4, IL-6,
IL-10, IL-12, tumor necrosis factor (TNF)-
, IFN-
, IL-8,
macrophage chemoattractant protein (MCP)-1, epithelial-neutrophil
activating peptide-78, vascular endothelial growth factor, and
thymidine phosphorylase (TP) were measured in 151 primary breast cancer
extracts by ELISA. Tumor-associated macrophages (TAMs) were also
examined by immunohistochemistry with anti-CD68 antibodies. The
correlation between soluble mediators and the relationship between TAM
count and soluble mediators were evaluated. MCP-1 concentration was
correlated significantly with the level of vascular endothelial growth
factor, TP, TNF-
, and IL-8, which are potent angiogenic factors.
IL-4 concentration was correlated significantly with IL-8 and IL-10. On
the other hand, an inverse association was observed between TP and
IL-12. The level of MCP-1 was associated significantly with TAM
accumulation. In the immunohistochemical analysis, MCP-1 expression was
observed in both infiltrating macrophages and tumor cells. Prognostic
analysis revealed that high expression of MCP-1, as well as of VEGF,
was a significant indicator of early relapse. These findings indicate
that interaction between the immune network system and angiogenesis is
important for progression of human breast cancer, and that MCP-1 may
play an important role in the regulation of angiogenesis and the immune
system.
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