High-infiltration of tumor-associated macrophages predicts unfavorable clinical outcome for node-negative breast cancer

PLoS One. 2013 Sep 30;8(9):e76147. doi: 10.1371/journal.pone.0076147. eCollection 2013.

Abstract

The tumor microenvironment is composed of tumor cells, fibroblasts, endothelial cells and infiltrating immune cells, which may inhibit or promote tumor growth and progression. The objectives of this retrospective study were to characterize the density of tumor-associated macrophages (TAMs) in breast cancer, and to correlate the density of TAMs with clinicopathological parameters. Paraffin-embedded specimens and clinicopathological data, including up to 5 years follow-up information, were obtained from 172 breast cancer patients. Immunohistochemical staining for CD68 (marker for macrophages) was performed and evaluated in a blinded fashion. We found that TAMs were significantly frequent in high histopathological grade breast cancer patients. Breast cancer patients with a high density of TAMs had significantly lower rates of disease-free survival and 5-year overall survival than patients with low density of TAMs. Furthermore, high-infiltration of TAMs indicated worse survival rate for patients with node-negative breast cancer. In conclusion, the number of TAMs in the tumor stroma is an independent predictor of survival time for breast cancer patients. High-infiltration of TAMs is a significant unfavorable prognostic factor for patients with invasive breast cancer and, as such, is a potentially useful prognostic marker for breast cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Biomarkers, Tumor / immunology*
  • Breast Neoplasms / immunology
  • Breast Neoplasms / physiopathology*
  • Disease-Free Survival
  • Female
  • Humans
  • Immunohistochemistry
  • Macrophages / immunology*
  • Prognosis
  • Retrospective Studies
  • Survival Rate
  • Tumor Microenvironment / immunology*

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers, Tumor
  • CD68 antigen, human

Grants and funding

The study was supported by Foundation of Educational Commission of Heilongjiang Province for Returned Overseas Chinese Scholars (1154h19). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.